HDAC4 (Protein|Antibody|cDNA Clone|ELISA Kit)

All HDAC4 reagents are produced in house and quality controlled, including 2 HDAC4 Antibody, 1 HDAC4 Gene, 1 HDAC4 IPKit, 1 HDAC4 Lysate, 1 HDAC4 Protein. All HDAC4 reagents are ready to use.

Recombinant HDAC4 proteins are expressed by Baculovirus-Insect Cells with fusion tags as N-GST & His, N-cleavage.

HDAC4 antibodies are validated with different applications, which are WB, ICC/IF, IF, IP, ELISA.

HDAC4 cDNA clones are full length sequence confirmed and expression validated. There are 13 kinds of tags for each HDAC4 of different species, especially GFP tag, OFP tag, FLAG tag and so on. There are three kinds of vectors for choice, cloning vector, expression vector and lentivrial expression vector.

HDAC4 Protein (1)


HDAC4 Protein, Human, Recombinant (aa 612-1084)


Expression host: Baculovirus-Insect Cells

Human HDAC4 Protein 9838

HDAC4 Antibody (2)

Application Clonality

Anti-HDAC4 Antibody


Specificity: Human

Application: WB,ICC/IF,IF,IP

Clonality: PAb

Human HDAC4 Immunohistochemistry(IHC) 3029

Anti-HDAC4 Antibody


Specificity: Human

Application: ELISA

Clonality: MAb


HDAC4 cDNA Clone (1)


HDAC4 IP Kit (1)

HDAC4 Lysate (1)

HDAC4 (histone deacetylase 4), belongs to class II of the histone deacetylase/acuc/apha family. Histone Deacetylases (HDACs) are a group of enzymes closely related to sirtuins. They catalyze the removal of acetyl groups from lysine residues in histones and non-histone proteins, resulting in transcriptional repression. In general, they do not act autonomously but as components of large multiprotein complexes, such as pRb-E2F and mSin3A, that mediate important transcription regulatory pathways. There are three classes of HDACs; classes 1, 2 and 4, which are closely related Zn2+-dependent enzymes. HDACs are ubiquitously expressed and they can exist in the nucleus or cytosol. Their subcellular localization is effected by protein-protein interactions and by the class to which they belong. HDACs have a role in cell growth arrest, differentiation and death and this has led to substantial interest in HDAC inhibitors as possible antineoplastic agents. HDAC4 possesses histone deacetylase activity and represses transcription when tethered to a promoter. It does not bind DNA directly, but through transcription factors MEF2C and MEF2D. HDAC4 seems to interact in a multiprotein complex with RbAp48 and HDAC3.