Anti-H2BK5ac Antibody | A2053

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone 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 is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack poly A tails; instead, they contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6p22-p21.3.

A2053 | Anti-H2BK5ac Antibody DataSheet

Antibody Target: H2BK5ac

Target Alternative Name: Histone H2B type 1-B (Histone H2B.1) (Histone H2B.f) (H2B/f), HIST1H2BB, H2BFF

Tag Line: Rabbit polyclonal antibody to detect acetylation of Histone H2B at Lysine 5 in human samples

Category: Primary antibody

Host: Rabbit

Isotype: IgG

Species Reactivities: Human

Immunogen Sequence: Acetylated peptide sequence targeting residues around Lysine 5 of human Histone H2B type 1-B

Accession #: P33778

Gene ID: 3018

Appearance: Colorless liquid

Form: Liquid

Concentration:

Formulation: In 0.01 M PBS, 50% glycerol, 0.03% proclin 300, pH 7.4

Purification: Antigen Affinity purified

Application: ChiP,Immunofluorescence (IF),Immunocytochemistry (ICC)

Positive Control:

Application And Usages: ICC,1:20-1:200, IF,1:50-1:200

Country of Animal Origin: USA

Country of Manufacture: USA

Usage: For Research Use Only! Not to be used in humans.

Handling: The antibody solution should be gently mixed before use.

Western Blot Verified: False

Immunocytochemistry Verified: True

Immunofluorescence Verified: True

Immunoprecipitation Verified: False

FACS Verified: False

ELISA Verified: False

ChIP Verified: True

Dot Blot Verified: False

Flow Cytometry Verified: False