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MilliporeSigma

EPI003

In Situ Histone Deacetylase (HDAC) Activity Fluorometric Assay Kit

100 assays in 96 well plates

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UNSPSC Code:
12352200
EC Number:
200-664-3
NACRES:
NA.41
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Nombre del producto

In Situ Histone Deacetylase (HDAC) Activity Fluorometric Assay Kit, 100 assays in 96 well plates

usage

100 assays in 96 well plates

shipped in

wet ice

storage temp.

−20°C

Application

In Situ Histone Deacetylase (HDAC) Activity Fluorometric Assay Kit has been used to determine HDAC activity.

Biochem/physiol Actions

Site specific histone acetylation and deacetylation have been shown to activate or repress eukaryotic gene transcription, respectively, and as a consequence, histone deacetylases (HDACs) play a crucial role in organism development and disease. Mutation or abnormal expression of HDAC is observed in cancer.

Features and Benefits

  • Simple two-step sensitive and reliable assay
  • All steps performed in the same cell culture plate
  • Utilizes fluorometric method
  • Sample type: cultured, adherent, and suspension cells
  • Suitable for individual tests or high throughput assays and kinetic studies
  • Convenient 96-well microplate format
  • Suitable for screening HDAC inhibitors or activators
  • Suitable for studying growth factors or other regulators that influence HDAC activity

General description

Histone deacetylases (HDACs) are a large family of enzymes that remove acetyl groups from histone proteins. HDACs are localized in both the cytosol and nucleus and some shuttle between the two locations.
Sigma′s InSitu HDAC Activity Fluorometric Assay Kit provides a direct, fast, fluorescence-based method to measure HDAC activity in cultured cells. The procedure requires just two steps, both performed in the original 96-well cell culture plate. First, the cell culture medium is replaced with a cell permeable HDAC Substrate, containing an acetylated lysine side chain. During the subsequent incubation, HDAC Substrate enters the cells and is deacetylated by intracellular HDAC. In the second step, Developer is added to lyse the cells and cleave the deacetylated HDAC Substrate to release a fluorophore. The fluorescence generated can be quantified at Ex/Em = 368/442 nm. The assay is well suited for either individual or high throughput screening.

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Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

Clase de almacenamiento

10 - Combustible liquids

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup


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Controlling the double helix.
Felsenfeld G and Groudine M
Nature, 421(6921), 448-448 (2003)
Influenza A virus dysregulates host histone deacetylase 1 that inhibits viral infection in lung epithelial cells.
Nagesh P T and Husain M
Journal of Virology (2016)
Qing-Shan Gao et al.
Zygote (Cambridge, England), 24(2), 236-244 (2015-05-01)
We investigated the effect of human induced pluripotent stem cell (hiPS) medium on porcine somatic cell nuclear transfer and bovine in vitro fertilized early blastocysts, in comparison with North Carolina State University (NCSU)-37 medium and in vitro culture (IVC)-II medium.
Long Jin et al.
Biotechnology letters, 38(9), 1433-1441 (2016-06-09)
To examine the effect of PCI-24781 (abexinostat) on the blastocyst formation rate in pig somatic cell nuclear transferred (SCNT) embryos and acetylation levels of the histone H3 lysine 9 and histone H4 lysine 12. Treatment with 0.5 nM PCI-24781 for 6 h
Christina Stache et al.
Neurosurgical focus, 41(6), E14-E14 (2016-12-03)
OBJECTIVE In this study, the authors investigated the underlying mechanisms responsible for high tumor recurrence rates of adamantinomatous craniopharyngioma (ACP) after radiotherapy and developed new targeted treatment protocols to minimize recurrence. ACPs are characterized by the activation of the receptor

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