7188570

HDAC2 Monoclonal Antibody (3F3), Active Motif™

Mouse Monoclonal Antibody

Manufacturer: Fischer Scientific

The price for this product is unavailable. Please request a quote

Antigen

HDAC2

Concentration

1 mg/mL

Classification

Monoclonal

Form

Liquid

Regulatory Status

RUO

Formulation

antibody with 30% glycerol and 0.035% sodium azide; pH

Gene Alias

BOS_9605; D10Wsu179e; HD2; HDAC2; Histone deacetylase 2; histone deacetylase 2-like protein; histone deacetylase-2; I79_010219; mRPD3; RPD3; transcriptional regulator homolog RPD3; YAF1; YY1 transcription factor-binding protein; YY1-associated factor 1; Yy1bp

Gene Symbols

HDAC2

Isotype

IgG1

Content And Storage

-20°C, Avoid Freeze/Thaw Cycles

Gene

HDAC2

Clone

3F3

Applications

Immunocytochemistry, Immunofluorescence, Western Blot

Conjugate

Unconjugated

Host Species

Mouse

Target Species

Human, Mouse, Rat

Gene Accession No.

P70288, Q92769

Gene ID (Entrez)

15182, 3066, 84577

Immunogen

This HDAC2 antibody was raised against a kLH-conjugated peptide corresponding to amino acids 473-488 of human HDAC2.

Primary or Secondary

Primary

Product Type

Antibody

Related Products

Img

Fischer Scientific

7188756

Mouse Monoclonal Antibody...

Img

Fischer Scientific

7188678

Mouse Monoclonal Antibody...

Img

Fischer Scientific

7188678

Mouse Monoclonal Antibody...

Img

Fischer Scientific

7188753

Rat Monoclonal Antibody...

Img

Fischer Scientific

7188517

Rat Monoclonal Antibody...

Img

Fischer Scientific

7188674

Mouse Monoclonal Antibody...

Img

Fischer Scientific

7188563

Mouse Monoclonal Antibody...

Img

Fischer Scientific

7188563

Mouse Monoclonal Antibody...

Description

  • The protein encoded by this gene is a member of the SWI/SNF family of proteins
  • Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes
  • The encoded protein shows sequence similarity to the E
  • coli RNA polymerase-binding protein HepA
  • Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency.