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Merck

CS1010

Sigma-Aldrich

Histone Deacetylase Assay Kit, Fluorometric

sufficient for 100 assays (96 well plates)

Synonim(y):

HDAC Assay Kit

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1 KIT
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5010,00 zł


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1 KIT
5010,00 zł

About This Item

Numer WE:
Kod UNSPSC:
12161503
NACRES:
NA.84

5010,00 zł


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zastosowanie

sufficient for 100 assays (96 well plates)

Poziom jakości

Warunki transportu

dry ice

temp. przechowywania

−20°C

informacje o genach

human ... HDAC1(3065)

Zastosowanie

The Histone Deacetylase Assay Kit provides a simple method for the detection of HDAC activity based on a two-step enzymatic reaction. The substrate for this enzymatic assay is a substituted peptide with an acetylated lysine residue and a bound fluorescent group. The first step of the reaction is deacetylation of the acetylated lysine side chain by the HDAC containing sample (HeLa cell extract, purified enzyme, etc.). The second step is the cleavage of the deacetylated substrate by the developer solution and the release of the free highly fluorescent group. The measured fluorescence is directly proportional to the deacetylation activity of the sample.

Działania biochem./fizjol.

Histone deacetylases (HDACs) are enzymes that remove acetyl groups from histone proteins. HDACs are important regulators of gene expression and genome function. They are implicated in a number of human disease states, namely several cancers, neurological disorders, and aging. Therefore, HDAC are relevant key targets for therapeutic intervention. Moreover, histone deacetylase inhibitors have been shown to serve as anti-tumor agents.

Cechy i korzyści

The kit includes all the reagents required for the fast and easy measurement of HDAC activity in cell or nuclear extracts, or with purified enzyme preparations. In addition, the kit provides HeLa cell lysate as a source of HDAC activity for inhibitor screening or as a positive control, a HDAC inhibitor (Trichostatin A), and a standard to enable activity quantitation.

Komentarz do analizy

The Histone Deacetylase Assay Kit has been tested on HeLa, HEK 293T, NIH 3T3, and U 973 cell extracts.
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Tylko elementy zestawu

Numer produktu
Opis

  • Assay Buffer 20 mL

  • Developer Solution 1.5 mL

  • HDAC Inhibitor (Trichostatin A), 1 mM 50 μL

  • HDAC Substrate, 20 mM 50 μL

  • HeLa Cell Lysate 500 μL

  • Standard (non-acetylated substrate), 4 mM 50 μL

Kod klasy składowania

10 - Combustible liquids

Temperatura zapłonu (°F)

188.6 °F - closed cup

Temperatura zapłonu (°C)

87 °C - closed cup


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Francis Wang Dang et al.
The Journal of biological chemistry, 291(36), 18765-18777 (2016-07-16)
The ubiquitin/proteasome pathway is a well characterized system for degrading intracellular proteins, although many aspects remain poorly understood. There is, for instance, a conspicuous lack of understanding of the site(s) where nuclear proteins are degraded because the subcellular distribution of
Ze Yang et al.
Cell research, 20(3), 276-287 (2010-01-27)
LSD1 (KDM1 under the new nomenclature) was the first identified lysine-specific histone demethylase belonging to the flavin-dependent amine oxidase family. Here, we report that AOF1 (KDM1B under the new nomenclature), a mammalian protein related to LSD1, also possesses histone demethylase
Lin Du et al.
Journal of natural products, 77(7), 1753-1757 (2014-07-08)
The cyclic tetrapeptide 1-alaninechlamydocin was purified from a Great Lakes-derived fungal isolate identified as a Tolypocladium sp. Although the planar structure was previously described, a detailed analysis of its spectroscopic data and biological activity are reported here for the first
Bartosz Bieszczad et al.
Pharmaceuticals (Basel, Switzerland), 14(9) (2021-09-29)
Histone deacetylase (HDAC) inhibitors are a class of drugs used in the cancer treatment. Here, we developed a library of 19 analogues of Vorinostat, an HDAC inhibitor used in lymphomas treatment. In Vorinostat, we replaced the hydrophobic phenyl group with
Jason D Plummer et al.
eLife, 10 (2021-03-31)
Methionine restriction (MR) dramatically extends the healthspan of several organisms. Methionine-restricted rodents have less age-related pathology and increased longevity as compared with controls, and recent studies suggest that humans might benefit similarly. Mechanistically, it is likely that the decreased IGF-1

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