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Histone H3-MeK9 AntibodyPurified Rabbit Polyclonal Antibody (Pab)

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AP1050a 0.1 mg 400 ul In Stock $ 255.00 Add to cart
AP1050a-ev20 20 ug 100 ul In Stock $ 95.00 Add to cart
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Histone H3-MeK9 Antibody - Product info

ApplicationDB
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionP84243
ReactivityHuman
Concentration0.25 mg/ml
IsotypeRabbit Ig
Calculated MW15328 Da

Histone H3-MeK9 Antibody - Additional info

Gene ID 3021
Other Names
H3F3A; H3.3A; H3F3; Histone H3.3
Target/Specificity
This Histone H3-MeK9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide methylated on K9(2 methyl groups) between 1~30 amino acids from aa 6~12 of human Histone 3.
Dilution
DB~~1:100~500
Format
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
Histone H3-MeK9 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.

Histone H3-MeK9 Antibody - Protein Information

Name H3F3A
Synonyms H3.3A, H3F3
Function
Variant histone H3 which replaces conventional H3 in a wide range of nucleosomes in active genes. Constitutes the predominant form of histone H3 in non-dividing cells and is incorporated into chromatin independently of DNA synthesis Deposited at sites of nucleosomal displacement throughout transcribed genes, suggesting that it represents an epigenetic imprint of transcriptionally active chromatin. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling
Cellular Location
Nucleus. Chromosome.

Histone H3-MeK9 Antibody - Related products

AM1151a: Phospho-Histone H3-S10 Antibody

AM1151b: Phospho-Histone H3-S10 Antibody

AM1151c: Phospho-Histone H3-S10 Antibody

AP1050a: Histone H3-MeK9 Antibody

AP1051a: Histone H3 (N-term)

AP1051d: Histone H3 Antibody (S10)

AP3667a: Phospho-H3-S10 Antibody

AP8890a: H3-S10 Antibody

AP9934a: Histone H3-K9 Antibody

RI12390: H3F3B predesign siRNA

DC00525: Human H3F3B cDNA Clone

LY11083a: H3F3B Over-expression Lysate

BP1050a: Histone H3-MeK9 Antibody Blocking Peptide

BP1051a: Histone H3 (N-term) Blocking Peptide

BP1051d: Histone H3 Antibody (S10) Blocking Peptide

BP3667a: Phospho-H3-S10 Antibody Blocking Peptide

BP8890a: H3-S10 Antibody Blocking Peptide

BP9934a: Histone H3-K9 Antibody Blocking Peptide

AJ1354a: Histone H3.3 Antibody Phospho (pS31)

AJ1358a: Histone-H3.3 Antibody Phospho-pS28&31

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BACKGROUND

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene for histone H3-MeK9 is intronless and encodes a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3.

REFERENCES

Marzluff, W.F., et al., Genomics 80(5):487-498 (2002). Albig, W., et al., Hum. Genet. 101(3):284-294 (1997). Albig, W., et al., Genomics 40(2):314-322 (1997). Albig, W., et al., Genomics 10(4):940-948 (1991).