Histone H2B Human, RecombinantProduct information
|100 µg ( 1 mg/ml )||-||Unavailable in your region|
Histone H2B combines with Histone H2A to form the H2A-H2B heterodimer. Two H2A/H2B heterodimers interact with an H3/H4 tetramer to form the histone octamer. Histone H2B is also modified by various enzymes and can act as a substrate for them. These modifications have been shown to be important in gene regulation.
Protein Sequence: PEPAK SAPAP KKGSK KAVTK AQKKD GKKRK RSRKE SYSIY VYKVL KQVHP DTGIS SKAMG IMNSF VNDIF ERIAG EASRL AHYNK RSTIT SREIQ TAVRL LLPGE LAKHA VSEGT KAVTK YTSSK(Genbank accession number: AAN59961)
Properties and Usage
300 mM NaCl
1 mM EDTA
20 mM sodium phosphate
pH 7.0 @ 25°C
Quality Control AssaysThe following Quality Control Tests are performed on each new lot and meet the specifications designated for the product. Individual lot data can be found on the Product Summary Sheet/Datacard or Manual which can be found in the Supporting Documents section of this page. Further information regarding NEB product quality can be found here.
- Endonuclease Activity (Nicking):
The product is tested in a reaction containing a supercoiled DNA substrate. After incubation for 4 hours the percent converted to the nicked form is determined by agarose gel electrophoresis.
- Exonuclease Activity (Radioactivity Release):
The product is tested in a reaction containing a radiolabeled mixture of single and double-stranded DNA. After incubation for 4 hours the exonuclease activity is determined by the % release of radioactive nucleotides.
- Molecular Weight Determination (Mass Spectrometry) :
The molecular weight of the product is determined using mass spectrometry.
- Protease Activity (SDS-PAGE):
The product is tested for protease activity by incubation with a standard mixture of proteins resulting in no detectable degradation of the proteins as determined by SDS-PAGE.
This product is covered by one or more patents, trademarks and/or copyrights owned or controlled by New England Biolabs, Inc (NEB).
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This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.
- 1 mg/ml, 73 µM is calculated using the molar extinction coefficient for Histone H2B (6400) and its absorbance at 280 nm (3,4). 1.0 A280 units = 2.2 mg/ml
- Kornberg, R.D. (1977). Annu. Rev. Biochem.. 46, 931-954.
- van Holde, K.E. (1989). Chromatin. 1-497.
- Gill, S.C. and von Hippel, P.H. (1988). Anal. Biochem.. 182, 319-326.
- Pace, C.N. et al. (1995). Protein Science. 4, 2411-2423.
The supporting documents available for this product can be downloaded below.