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H2662

Sigma-Aldrich

Anti-Histone Deacetylase 7 (HDAC7) (KG-17) antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

Sinonimo/i:

Anti-HD7, Anti-HD7A, Anti-HDAC7A

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About This Item

Numero MDL:
Codice UNSPSC:
12352203
NACRES:
NA.41

Origine biologica

rabbit

Livello qualitativo

Coniugato

unconjugated

Forma dell’anticorpo

affinity isolated antibody

Tipo di anticorpo

primary antibodies

Clone

polyclonal

Forma fisica

buffered aqueous solution

PM

antigen ~105 kDa

Reattività contro le specie

mouse, human, rat

tecniche

immunoprecipitation (IP): 1.0-1.5 μg using RIPA extract of 293T cells expressing recombinant human HDAC7
indirect immunofluorescence: 1:50 using rat NRK cells
western blot: 1:1,000 using whole extracts of mouse NIH-3T3 cells

N° accesso UniProt

Condizioni di spedizione

dry ice

Temperatura di conservazione

−20°C

modifica post-traduzionali bersaglio

unmodified

Informazioni sul gene

human ... HDAC7(51564)
mouse ... Hdac7(56233)
rat ... Hdac7a(84582)

Descrizione generale

Mammalian histone deacetylases (HDACs) can be divided into three classes according to sequence homology. Class I consists of the yeast transcriptional regulatory protein Rpd3-like proteins HDAC1, HDAC2, HDAC3, and HDAC8. Class II consists of the yeast Hda1-like proteins HDAC4, HDAC5, HDAC6, HDAC7, HDAC9 and HDAC10. Class III consists of the yeast sirtuin 2 (Sir2)-like proteins. Although HDAC7 is localized mostly to the cell nucleus, it is also found in the cytoplasm.

Specificità

Anti-Histone Deacetylase 7 recognizes human, mouse, and rat HDAC7.

Immunogeno

Synthetic peptide corresponding to amino acids of human HDAC7, conjugated to KLH.

Applicazioni

Anti-Histone Deacetylase 7 (HDAC7) (KG-17) antibody produced in rabbit has been used in
  • indirect immunofluorescene
  • immunoblotting
  • immunoprecipitation

Azioni biochim/fisiol

Class II histone deacetylases (HDACs) have been implicated in the regulation of muscle differentiation. Interaction of HDAC4, -5, and -7 with members of the myocyte enhancer factor-2 (Mef2) family of transcription factors represses their transcriptional activity and prevents myogenesis. Shuttling of HDAC7 between the cell nucleus and the cytoplasm is controlled by a mechanism involving calmodulin independent kinase I (CaMKI) and 14-3-3 proteins. The HDAC7 enzymatic activity depends on its interaction with the class I HDAC3, and the corepressors silencing mediator of retinoic acid and thyroid hormone receptors (SMRT) and nuclear receptor co-repressor (N-COR). HDAC7 also interacts with the transcriptional repressor B-cell lymphoma 6 (BCL-6).

Stato fisico

Solution in 0.01 M phosphate buffered saline containing 1% bovine serum albumin and 15 mM sodium azide.

Esclusione di responsabilità

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

nwg

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

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Class II histone deacetylases are directly recruited by BCL6 transcriptional repressor
Lemercier C, et al.
Test, 277(24), 22045-22052 (2002)
Splicing of HDAC7 modulates the SRF-myocardin complex during stem-cell differentiation towards smooth muscle cells
Margariti A, et al.
Journal of Cell Science, 122(4), 460-470 (2009)
Erasers of histone acetylation: the histone deacetylase enzymes
Seto E and Yoshida M
Cold Spring Harbor Perspectives in Biology, 6(4), a018713-a018713 (2014)
Human HDAC7 Histone Deacetylase Activity Is Associated with HDAC3in Vivo
Fischle W, et al.
Test, 276(38), 35826-35835 (2001)
Caroline L Benn et al.
PloS one, 4(6), e5747-e5747 (2009-06-02)
Huntington's disease (HD) is an inherited, progressive neurological disorder caused by a CAG/polyglutamine repeat expansion, for which there is no effective disease modifying therapy. In recent years, transcriptional dysregulation has emerged as a pathogenic process that appears early in disease

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