|Application ||WB, FC, E|
|Other Accession||Q9JHD2, NP_066564|
|Calculated MW||93926 Da|
|Antigen Region||807-837 aa|
|Other Names||Histone acetyltransferase KAT2A, General control of amino acid synthesis protein 5-like 2, Histone acetyltransferase GCN5, HsGCN5, Lysine acetyltransferase 2A, STAF97, KAT2A, GCN5, GCN5L2, HGCN5|
|Target/Specificity||This hGCN5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 807-837 amino acids from the C-terminal region of human hGCN5.|
|Format||Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.|
|Storage||Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||hGCN5 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Synonyms||GCN5, GCN5L2, HGCN5|
|Function||Functions as a histone acetyltransferase (HAT) to promote transcriptional activation. Acetylation of histones gives a specific tag for epigenetic transcription activation. Has significant histone acetyltransferase activity with core histones, but not with nucleosome core particles. In case of HIV-1 infection, it is recruited by the viral protein Tat. Regulates Tat's transactivating activity and may help inducing chromatin remodeling of proviral genes. Component of the ATAC complex, a complex with histone acetyltransferase activity on histones H3 and H4.|
|Tissue Location||Expressed in all tissues tested, with most abundant expression in ovary|
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Provided below are standard protocols that you may find useful for product applications.
KAT2A, or GCN5, is a histone acetyltransferase (HAT) that functions primarily as a transcriptional activator. It also functions as a repressor of NF-kappa-B (see MIM 164011) by promoting ubiquitination of the NF-kappa-B subunit RELA (MIM 164014) in a HAT-independent manner (Mao et al., 2009 [PubMed 19339690]).
Terreni, M., et al. Retrovirology 7, 18 (2010) :
Atanassov, B.S., et al. Mol. Cell 35(3):352-364(2009)
Kelly, T.J., et al. J. Biol. Chem. 284(30):19945-19952(2009)
Mao, X., et al. Genes Dev. 23(7):849-861(2009)
Paolinelli, R., et al. Nat. Struct. Mol. Biol. 16(4):412-420(2009)
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