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Merck
CN

17-320

Histone Deacetylase Assay Kit (HDAC)

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UNSPSC Code:
12161503
NACRES:
NA.84
eCl@ss:
32161000
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technique(s)

enzyme immunoassay: suitable

UniProt accession no.

Quality Level

General description

FUNCTION: SwissProt: Q9UQL6 # Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation by repressing transcription of myocyte enhancer MEF2C. During muscle differentiation, it shuttles into the cytoplasm, allowing the expression of myocyte enhancer factors.
SIZE: 1122 amino acids; 121992 Da
SUBUNIT: Interacts with BCOR, HDAC7, HDAC9, CTBP1, MEF2C, NCOR2, NRIP1, PHB2 and a 14-3-3 chaperone protein. Interacts with JARID1B.
SUBCELLULAR LOCATION: Nucleus. Cytoplasm. Note=Shuttles between the nucleus and the cytoplasm. In muscle cells, it shuttles into the cytoplasm during myocyte differentiation. The export to cytoplasm depends on the interaction with a 14-3-3 chaperone protein and is due to its phosphorylation at Ser-259 and Ser-498 by CaMK.TISSUE SPECIFICITY: Ubiquitous.DOMAIN:SwissProt: Q9UQL6 The nuclear export sequence mediates the shuttling between the nucleus and the cytoplasm (By similarity).
PTM: Phosphorylated by CaMK at Ser-259 and Ser-498. The phosphorylation is required for the export to the cytoplasm. & Ubiquitinated. Polyubiquitination however does not lead to its degradation.
SIMILARITY: Belongs to the histone deacetylase family. Type 2 subfamily.

Packaging

Kit capacity: 100 assays

Analysis Note

Routinely evaluated with two experiments, The dependence of HDAC activity on HeLa Nuclear Extract and the inhibition of HDAC Activity by Sodium Butyrate.

In the first experiment, HeLa nuclear extract was incubated at room temperature with [3H]-acetyl-Histone H4 peptide. Released [3H]-acetate was measured using a scintillation counter.

In the second experiment, [3H]-acetyl-Histone H4 peptide was incubated with HeLa nuclear extract in the presence or absence of Sodium Butyrate. Sodium Butyrate inhibited release of [3H]-acetate by ~92%.

Other Notes

HeLa NuCLEAR Extract (Cat.# 12-309) Histone H4 Peptide, biotin conjugate, residues 2-24 (Cat.# 12-372) HAT Assay Buffer, 5X (Cat.# 20-148) Sodium Butyrate (Cat.# 19-137) 5X HDAC Assay Buffer Streptavidin Agarose PCAF active

Legal Information

NuCLEAR is a trademark of Sigma-Aldrich Co. LLC

Disclaimer

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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相关内容

"Epigenetics describes heritable changes in gene expression caused by non-genetic mechanisms instead of by alterations in DNA sequence. These changes can be cell- or tissue-specific, and can be passed on to multiple generations. Epigenetic regulation enriches DNAbased information, allowing a cell to vary its response across diverse biological and environmental contexts. Although epigenetic mechanisms are primarily centered in the nucleus, these mechanisms can be induced by environmental signals such as hormones, nutrients, stress, and cellular damage, pointing to the involvement of cytoplasmic and extracellular factors in epigenetic regulation."

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