Human H1(Histone H1) ELISA Kit

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Histone H1 (H1) in tissue homogenates, cell lysates and other biological fluids.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Histone H1 (H1) in tissue homogenates, cell lysates and other biological fluids.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Histone H1 (H1) in tissue homogenates, cell lysates and other biological fluids.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Histone H1 (H1) in tissue homogenates, cell lysates and other biological fluids.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Human Histone H1 (H1) in samples from tissue homogenates, cell lysates and other biological fluids with no significant corss-reactivity with analogues from other species.

Description: A sandwich ELISA kit for detection of Histone H1 from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: Recombinant Human Histone H1 expressed in: E.coli

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a Blasticidin marker under Rsv promoter.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a Puromycin marker under Rsv promoter.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a GFP-Blasticidin fusion marker under Rsv promoter.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a GFP-Puromycin fusion marker under Rsv promoter.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a RFP-Blasticidin fusion marker under Rsv promoter.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a RFP-puromycin fusion marker under Rsv promoter.

Description: Purified Polyclonal Histone H1 antibody

Description: Rabbit polyclonal Histone H1 antibody

Description: A polyclonal antibody against Histone H1. Recognizes Histone H1 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: WB;WB:1:1000-2000

Description: A polyclonal antibody against Histone H1. Recognizes Histone H1 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: WB, IHC, IF, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.IF:1/200-1/1000.ELISA:1/20000

Description: Mouse polyclonal to Histone H1

Description: Mouse polyclonal to Histone H1

Description: Mouse polyclonal to Histone H1

Description: Rabbit polyclonal to Histone H1

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Five major families of histones exist: H1/H5, H2A, H2B, H3, and H4. Histones H2A, H2B, H3 and H4 are known as the core histones, while histones H1/H5 are known as the linker histones. The core histones all exist as dimers, which are similar in that they all possess the histone fold domain; three alpha helices linked by two loops. It is this helical structure that allows for interaction between distinct dimers, particularly in a head-tail fashion (also called the handshake motif). The linker histone H1 binds the nucleosome at the entry and exit sites of the DNA, thus locking the DNA into place and allowing the formation of higher order structure. [Wiki]

Description: Five major families of histones exist: H1/H5, H2A, H2B, H3, and H4. Histones H2A, H2B, H3 and H4 are known as the core histones, while histones H1/H5 are known as the linker histones. The core histones all exist as dimers, which are similar in that they all possess the histone fold domain; three alpha helices linked by two loops. It is this helical structure that allows for interaction between distinct dimers, particularly in a head-tail fashion (also called the handshake motif). The linker histone H1 binds the nucleosome at the entry and exit sites of the DNA, thus locking the DNA into place and allowing the formation of higher order structure. [Wiki]

Description: Five major families of histones exist: H1/H5, H2A, H2B, H3, and H4. Histones H2A, H2B, H3 and H4 are known as the core histones, while histones H1/H5 are known as the linker histones. The core histones all exist as dimers, which are similar in that they all possess the histone fold domain; three alpha helices linked by two loops. It is this helical structure that allows for interaction between distinct dimers, particularly in a head-tail fashion (also called the handshake motif). The linker histone H1 binds the nucleosome at the entry and exit sites of the DNA, thus locking the DNA into place and allowing the formation of higher order structure. [Wiki]

Description: Five major families of histones exist: H1/H5, H2A, H2B, H3, and H4. Histones H2A, H2B, H3 and H4 are known as the core histones, while histones H1/H5 are known as the linker histones. The core histones all exist as dimers, which are similar in that they all possess the histone fold domain; three alpha helices linked by two loops. It is this helical structure that allows for interaction between distinct dimers, particularly in a head-tail fashion (also called the handshake motif). The linker histone H1 binds the nucleosome at the entry and exit sites of the DNA, thus locking the DNA into place and allowing the formation of higher order structure. [Wiki]

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. Histones are subject to posttranslational modification by enzymes primarily on their N-terminal tails, but also in their globular domains. Such modifications include methylation, citrullination, acetylation, phosphorylation, sumoylation, ubiquitination and ADP-ribosylation.

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Histones H1 are necessary for the condensation of nucleosome chains into higher-order structures. The H1F0 histones are found in cells that are in terminal stages of differentiation or that have low rates of cell division. [UniProt]

Description: Please note that this antibody is a recombinant mouse version of original anti-histone H1 antibody (clone AE-4). Because the variable heavy (VH) and variable light (VL) domains are the same, this recombinant antibody has the same exact reactivity as the original AE-4 MAb. There are several advantages of producing a recombinant version of a monoclonal antibody. For example, a recombinant antibody is a purer preparation of active immunoglobulin with no contaminating non-functional intact Ig or free light/heavy chains. Secondly, antibody can always be produced, even if hybridoma line is lost. Moreover, it adds the flexibility of converting the antibody to any species, isotype or format.Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. This antibody is extensively used as a pan-nuclear marker.

Description: Please note that this antibody is a recombinant mouse version of original anti-histone H1 antibody (clone AE-4). Because the variable heavy (VH) and variable light (VL) domains are the same, this recombinant antibody has the same exact reactivity as the original AE-4 MAb. There are several advantages of producing a recombinant version of a monoclonal antibody. For example, a recombinant antibody is a purer preparation of active immunoglobulin with no contaminating non-functional intact Ig or free light/heavy chains. Secondly, antibody can always be produced, even if hybridoma line is lost. Moreover, it adds the flexibility of converting the antibody to any species, isotype or format.Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. This antibody is extensively used as a pan-nuclear marker.

Description: Please note that this antibody is a recombinant mouse version of original anti-histone H1 antibody (clone AE-4). Because the variable heavy (VH) and variable light (VL) domains are the same, this recombinant antibody has the same exact reactivity as the original AE-4 MAb. There are several advantages of producing a recombinant version of a monoclonal antibody. For example, a recombinant antibody is a purer preparation of active immunoglobulin with no contaminating non-functional intact Ig or free light/heavy chains. Secondly, antibody can always be produced, even if hybridoma line is lost. Moreover, it adds the flexibility of converting the antibody to any species, isotype or format.Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. This antibody is extensively used as a pan-nuclear marker.

Description: Please note that this antibody is a recombinant rabbit version of original anti-histone H1 antibody (clone AE-4). Because the variable heavy (VH) and variable light (VL) domains are the same, this recombinant antibody has the same exact reactivity as the original AE-4 MAb. There are several advantages of producing a recombinant version of a monoclonal antibody. For example, a recombinant antibody is a pure preparation of active immunoglobulin with no contaminating non-functional intact Ig or free light/heavy chains. Secondly, antibody can always be produced, even if hybridoma line is lost. Moreover, it adds the flexibility of converting the antibody to any species, isotype or format. Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. This antibody is extensively used as a pan-nuclear marker.

Description: Please note that this antibody is a recombinant rabbit version of original anti-histone H1 antibody (clone AE-4). Because the variable heavy (VH) and variable light (VL) domains are the same, this recombinant antibody has the same exact reactivity as the original AE-4 MAb. There are several advantages of producing a recombinant version of a monoclonal antibody. For example, a recombinant antibody is a pure preparation of active immunoglobulin with no contaminating non-functional intact Ig or free light/heavy chains. Secondly, antibody can always be produced, even if hybridoma line is lost. Moreover, it adds the flexibility of converting the antibody to any species, isotype or format. Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. This antibody is extensively used as a pan-nuclear marker.

Description: Please note that this antibody is a recombinant rabbit version of original anti-histone H1 antibody (clone AE-4). Because the variable heavy (VH) and variable light (VL) domains are the same, this recombinant antibody has the same exact reactivity as the original AE-4 MAb. There are several advantages of producing a recombinant version of a monoclonal antibody. For example, a recombinant antibody is a pure preparation of active immunoglobulin with no contaminating non-functional intact Ig or free light/heavy chains. Secondly, antibody can always be produced, even if hybridoma line is lost. Moreover, it adds the flexibility of converting the antibody to any species, isotype or format. Eukaryotic histones are basic and water-soluble nuclear proteins that form hetero-octameric nucleosome particles by wrapping 146 base pairs of DNA in a left-handed super-helical turn sequentially to form chromosomal fiber. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form the octamer; formed of two H2A-H2B dimers and two H3-H4 dimers, forming two nearly symmetrical halves by tertiary structure. Over 80% of nucleosomes contain the linker Histone H1, derived from an intronless gene that interacts with linker DNA between nucleosomes and mediates compaction into higher order chromatin. This antibody is extensively used as a pan-nuclear marker.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a GFP-Blasticidin fusion marker under Rsv promoter. Virus was concentrated and provided in PBS solution.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a GFP-Puromycin fusion marker under Rsv promoter. Virus was concentrated and provided in PBS solution.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a RFP-Blasticidin fusion marker under Rsv promoter. Virus was concentrated and provided in PBS solution.

Description: Pre-made optional inducible lentiviral shRNA expression particles under human H1 promoter, containing a hairpin insert that should not knockdown any known human or mouse gene. This non-targeting control serves as a negative control for shRNA knockdown experiments. It also contains a RFP-puromycin fusion marker under Rsv promoter. Virus was concentrated and provided in PBS solution.

Description: Rabbit Polyclonal Antibody for Histone H1 Antibody (HIST1H1B) detection.tested for WB in Human, Mouse.

Description: Rabbit polyclonal Histone H1 antibody (Thr17)

Description: A polyclonal antibody for detection of Histone H1 from Human, Mouse. This Histone H1 antibody is for WB. It is affinity-purified from rabbit antiserum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthetic peptide

Description: A polyclonal antibody for detection of Histone H1 from Human, Mouse. This Histone H1 antibody is for WB. It is affinity-purified from rabbit antiserum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthetic peptide

Description: A polyclonal antibody for detection of Histone H1 from Human, Mouse. This Histone H1 antibody is for WB. It is affinity-purified from rabbit antiserum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthetic peptide

Description: A polyclonal antibody for detection of Histone H1 from Human. This Histone H1 antibody is for IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human Histone H1 around the non-acetylation site of K25 at AA rangle: 100-180

Description: A polyclonal antibody for detection of Histone H1 from Human. This Histone H1 antibody is for IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human Histone H1 around the non-acetylation site of K25 at AA rangle: 100-180

Description: A polyclonal antibody for detection of Histone H1 from Human. This Histone H1 antibody is for IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human Histone H1 around the non-acetylation site of K25 at AA rangle: 100-180

Description: A polyclonal antibody for detection of Histone H1 from Human, Mouse. This Histone H1 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human Histone H1 around the non-phosphorylation site of T17

Description: A polyclonal antibody for detection of Histone H1 from Human, Mouse. This Histone H1 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human Histone H1 around the non-phosphorylation site of T17

Description: A polyclonal antibody for detection of Histone H1 from Human, Mouse. This Histone H1 antibody is for WB, IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human Histone H1 around the non-phosphorylation site of T17

Description: A Rabbit Polyclonal antibody against Histone H1 from Human/Mouse. This antibody is tested and validated for WB, ELISA, IHC, IF, WB, ELISA

Description: A Rabbit Polyclonal antibody against Histone H1 from Human/Mouse. This antibody is tested and validated for WB, ELISA, IHC, IF, WB, ELISA

Description: A Rabbit Polyclonal antibody against Histone H1 from Human/Mouse. This antibody is tested and validated for WB, ELISA

Description: A Rabbit Polyclonal antibody against Histone H1 from Human/Mouse. This antibody is tested and validated for WB, ELISA

Description: A Rabbit Polyclonal antibody against Histone H1 from Human. This antibody is tested and validated for IHC, IF, WB, ELISA

Description: A Rabbit Polyclonal antibody against Histone H1 from Human. This antibody is tested and validated for IHC, IF, WB, ELISA

Description: Antibody raised against Histone H1

Description: Rabbit polyclonal to Histone H1.

Description: Rabbit polyclonal to Histone H1.

Description: Rabbit polyclonal to Histone H1.

Description: Primary antibody against Histone H1(AE-4), CF405S conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF405S conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF405S conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF405S conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF405S conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF405S conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF405M conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF405M conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF405M conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF405M conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF405M conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF405M conjugate, Concentration: 0.1mg/mL

Description: A polyclonal antibody against Phospho-Histone H1 (Ser1). Recognizes Phospho-Histone H1 (Ser1) from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB;WB:1:1000-2000

Description: A polyclonal antibody against Phospho-Histone H1 (Thr3). Recognizes Phospho-Histone H1 (Thr3) from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB;WB:1:1000-2000

Description: A polyclonal antibody against Phospho-Histone H1 (Thr17). Recognizes Phospho-Histone H1 (Thr17) from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB;WB:1:1000-2000

Description: Primary antibody against Histone H1(AE-4), Alkaline Phosphatase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), Alkaline Phosphatase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), Alkaline Phosphatase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), Alkaline Phosphatase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), Alkaline Phosphatase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), Alkaline Phosphatase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), Biotin conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), Biotin conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), Biotin conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), Biotin conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), Biotin conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), Biotin conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), PerCP conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), PerCP conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), PerCP conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), RPE conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), RPE conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), RPE conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF594 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF594 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF594 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF594 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF594 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF594 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), APC conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), APC conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), APC conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF680R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF680R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF680R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF680R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF680R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF680R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), Concentration: 0.2mg/mL

Description: Primary antibody against Histone H1(AE-4), Concentration: 0.2mg/mL

Description: Primary antibody against Histone H1(1415--1), Concentration: 0.2mg/mL

Description: Primary antibody against Histone H1(1415--1), Concentration: 0.2mg/mL

Description: Primary antibody against Histone H1(HH1/957), Concentration: 0.2mg/mL

Description: Primary antibody against Histone H1(HH1/957), Concentration: 0.2mg/mL

Description: Primary antibody against Histone H1(AE-4), Horseradish Peroxidase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), Horseradish Peroxidase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), Horseradish Peroxidase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), Horseradish Peroxidase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), Horseradish Peroxidase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), Horseradish Peroxidase conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF488A conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF488A conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF488A conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF488A conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF488A conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF488A conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF568 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF568 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF568 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF568 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF568 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF568 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF647 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF647 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF647 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF647 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF647 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF647 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF640R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF640R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF640R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF640R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF543 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF543 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF543 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF543 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF543 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF543 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF555 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF555 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF555 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF555 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF660R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF660R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF660R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF660R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF660R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF660R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF680 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF680 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF680 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF680 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF680 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF680 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF640R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF640R conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF770 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(HH1/957), CF770 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF555 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF555 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF770 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(AE-4), CF770 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF770 conjugate, Concentration: 0.1mg/mL

Description: Primary antibody against Histone H1(1415--1), CF770 conjugate, Concentration: 0.1mg/mL