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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

Histone H1.4 (D4J5Q) Rabbit mAb #41328

Filter:
  • WB
  • IF
  • ChIP

    Supporting Data

    REACTIVITY H Mk
    SENSITIVITY Endogenous
    MW (kDa) 30
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    • IF-Immunofluorescence 
    • ChIP-Chromatin Immunoprecipitation 
    Species Cross-Reactivity Key:
    • H-Human 
    • Mk-Monkey 

    Product Information

    Product Usage Information

    For optimal ChIP results, use 10 μl of antibody and 10 μg of chromatin (approximately 4 x 106 cells) per IP. This antibody has been validated using SimpleChIP® Enzymatic Chromatin IP Kits.

    Application Dilution
    Western Blotting 1:1000
    Immunofluorescence (Immunocytochemistry) 1:200 - 1:800
    Chromatin IP 1:50

    Storage

    Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

    Protocol

    Specificity / Sensitivity

    Histone H1.4 (D4J5Q) Rabbit mAb recognizes endogenous levels of total histone H1.4 protein. This antibody also cross reacts with histone H1.5 (UniProt P16401) and weakly with histones H1.1 (UniProt Q02539), H1.2 (UniProt P16403), and H1.3 (UniProt P16402).


    Species Reactivity:

    Human, Monkey


    The antigen sequence used to produce this antibody shares 100% sequence homology with the species listed here, but reactivity has not been tested or confirmed to work by CST. Use of this product with these species is not covered under our Product Performance Guarantee.

    Species predicted to react based on 100% sequence homology:

    Hamster, Bovine, Dog

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala176 of human histone H1.4 protein.

    Background

    Histones are evolutionarily conserved proteins that play a vital role in the compaction, storage, and regulation of DNA within the eukaryotic nucleus. The basic subunit of chromatin, the nucleosome core particle, is composed of DNA wound around two copies each of the core histone proteins H2A, H2B, H3, and H4 (1-3). Formation of higher order chromatin structure is facilitated through the binding of linker histone H1 to the nucleosome particle (chromatosome) (4-6). In humans and mice, there are 11 distinct histone H1 variants, which include the somatic variants (H1.1, H1.2, H1.3, H1.4, and H1.5) that are expressed ubiquitously, and cell type specific variants such as H1t found in the testis and H1.0 expressed in terminally differentiated cells (6-10). Binding of histone H1 to chromatin limits accessibility of DNA to other proteins by stabilizing nucleosome positioning, competing for binding sites, and limiting the activity of chromatin remodeling proteins such as the SWI/SNF complex (6,11-14). Histone H1 binding is highly dynamic and is thought to be regulated by post-translational modifications (6). For example, cell cycle regulated phosphorylation of histone H1 leads to chromatin condensation and decondensation depending on the site of phosphorylation and histone H1.4 Lys34 acetylation by GCN5 has been linked to increased mobility of H1.4 and transcriptional activation (6, 15-18).

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    4. Thoma, F. et al. (1979) J Cell Biol 83, 403-27.
    5. Carruthers, L.M. et al. (1998) Biochemistry 37, 14776-87.
    6. Harshman, S.W. et al. (2013) Nucleic Acids Res 41, 9593-609.
    7. Eick, S. et al. (1989) Eur J Cell Biol 49, 110-5.
    8. Carozzi, N. et al. (1984) Science 224, 1115-7.
    9. Drabent, B. et al. (1991) Gene 103, 263-8.
    10. Pehrson, J.R. and Cole, R.D. (1982) Biochemistry 21, 456-60.
    11. Bustin, M. et al. (2005) Mol Cell 17, 617-20.
    12. Hill, D.A. and Imbalzano, A.N. (2000) Biochemistry 39, 11649-56.
    13. Ramachandran, A. et al. (2003) J Biol Chem 278, 48590-601.
    14. Horn, P.J. et al. (2002) Nat Struct Biol 9, 263-7.
    15. Hohmann, P. et al. (1976) J Biol Chem 251, 3685-92.
    16. D'Anna, J.A. et al. (1978) Nucleic Acids Res 5, 3195-207.
    17. Matsumoto, Y. et al. (1980) Nature 284, 181-3.
    18. Kamieniarz, K. et al. (2012) Genes Dev 26, 797-802.
    For Research Use Only. Not For Use In Diagnostic Procedures.
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