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Sigma-Aldrich

Acetyl-Histone H4 (Lys8) Peptide

Acetyl-Histone H4 (Lys8) Peptide primarily used in Histone Acetyltransferase Assays (HAT) and Western Blotting.

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About This Item

UNSPSC Code:
12352202
eCl@ss:
32160405
NACRES:
NA.42

Quality Level

form

liquid

manufacturer/tradename

Upstate®

technique(s)

activity assay: suitable (histone acetyltransferase (HAT))
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

dry ice

Application

Acetyl-Histone H4 (Lys8) Peptide primarily used in Histone Acetyltransferase Assays (HAT) and Western Blotting.

Quality

Routinely evaluated by Dot Blot Analysis. This peptide was used as a standard to assess the specificity of anti-acetyl histone antibodies for acetyl lysine 8 of Histone H4.

Physical form

sterile deionized water

Storage and Stability

2 years at -20°C

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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.

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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MCP-1 promotes mural cell recruitment during angiogenesis in the aortic ring model.
Alfred C Aplin,Eric Fogel,Roberto F Nicosia
Angiogenesis null
C A Mizzen et al.
Cell, 87(7), 1261-1270 (1996-12-27)
The transcription initiation factor TFIID is a multimeric protein complex composed of TATA box-binding protein (TBP) and many TBP-associated factors (TAF(II)s). TAF(II)s are important cofactors that mediate activated transcription by providing interaction sites for distinct activators. Here, we present evidence

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