Histone, acetylated BioAssay™ Sample Kit

Referencia H5110-05-8x20ul

embalaje : 8x20ul

Marca : US Biological



H5110-05 Histone, acetylated BioAssay™ Sample Kit

Shipping Temp
Blue Ice
Storage Temp
-20°C

The Acetyl-Histone Antibody Sampler Kit provides a fast and economical means to evaluate the activation status of the acetylation sites on all of the histones. The kit contains enough primary and secondary antibodies to perform two mini-blot experiments.

Modulation of the chromatin structure plays an important role in the regulation of transcription in eukaryotes. The nucleosome, made up of four core histone proteins (H2A, H2B, H3 and H4), is the primary building block of chromatin (1). The N-terminal tail of core histones undergoes different posttranslational modifications including acetylation, phosphorylation and methylation (2-4). These modifications occur in response to cell signal stimuli and have a direct effect on gene expression. In most species, the histone H2B is primarily acetylated at lysines 5, 12, 15 and 20 (4,5). Histone H3 is primarily acetylated at lysines 9, 14, 18 and 23 (2,3). Acetylation at lysine 9 appears to have a dominant role in histone deposition and chromatin assembly in some organisms (2,3). Phosphorylation at Ser10 of histone H3 is tightly correlated with chromosome condensation during both mitosis and meiosis (6).

Applications
Purity: Purified by Protein A and peptide affinity chromatography.|Form: Supplied as a liquid in 10mM sodium HEPES, pH 7.5, 150mM sodium chloride, 0.1mg/ml BSA, 50% glycerol.|Specificity: Note: Adherence to the attached protocol is extremely important.||Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Form
Supplied as a liquid in 10mM sodium HEPES, pH 7.5, 150mM sodium chloride, 0.1mg/ml BSA, 50% glycerol.
Purity
Purified by Protein A and peptide affinity chromatography.
Specificity
Note: Adherence to the attached protocol is extremely important.
References
Background References: (1) Workman, J.L. and Kingston, R.E. (1998) Annu. Rev. Biochem. 67, 545–579. (2) Hansen, J. C. et al. (1998) Biochemistry 37, 17637–17641. (3) Strahl, B.D. and Allis, C.D. (2000) Nature 403, 41–45. (4) Cheung, P. et al. (2000) Cell 103, 263–271. (5) Thorne, A. W. et al. (1990) Eur. J. Biochem. 193, 701–713. (6) Hendzel, M. J. et al. (1997) Chromosoma 106, 348–360.