General description
P2334-200ml′更新后的产品编号为GE17-0965-05
Application
苯基[YM=“琼脂糖”]可用于蛋白质层析、亲和层析、疏水相互作用介质、树脂和分离介质。苯基-琼脂糖™已被用于促进去污剂和饲料工业中添加剂工业应用改善的研究中。苯基-琼脂糖还被用于研究存在微生物菌群的高盐环境。
Physical form
悬浮于20%乙醇中
乙醇-水混悬液
Legal Information
Sepharose is a trademark of Cytiva
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
95.0 °F
flash_point_c
35 °C
法规信息
危险化学品
此项目有
P D Zschocke et al.
European journal of biochemistry, 213(1), 263-269 (1993-04-01)
A purification procedure for guanylate kinase from pig brain has been developed consisting of ammonium sulfate precipitation and heptane extraction of the crude extract, hydrophobic-interaction chromatography, affinity chromatography and chromatofocussing. From 1.75 kg pig brain, 1.2 mg enzyme was isolated
Agnes Marot-Leblond et al.
Journal of clinical microbiology, 44(1), 138-142 (2006-01-05)
Cell components of the dimorphic pathogenic fungus Candida dubliniensis were used to prepare monoclonal antibodies (MAbs). One MAb, designated 12F7-F2, was shown by indirect immunofluorescence to be specific for a surface antigen of Candida dubliniensis yeast cells. No reactivity was
J L Blank et al.
The Journal of biological chemistry, 268(33), 25184-25191 (1993-11-25)
We report the purification from bovine brain cytosol of a 110-kDa phosphoinositide-specific phospholipase C (PLC-110) that was markedly stimulated by G-protein beta gamma-subunits. The enzyme was purified approximately 2000-fold with a yield of 4%. On the basis of size and
Jace L Fogle et al.
Journal of chromatography. A, 1121(2), 209-218 (2006-05-13)
Amide hydrogen-deuterium exchange labeling has been used to study the effects of salt and protein loading on alpha-lactalbumin (BLA) stability during hydrophobic interaction chromatography (HIC). Stability in the adsorbed phase increased dramatically with increasing loading, and unfolding was nearly undetectable
Teresa Martínez-Cortés et al.
Plant physiology and biochemistry : PPB, 52, 130-139 (2012-02-07)
Two cationic peroxidases from Selaginella martensii Spring. (SmaPrx2 and SmaPrx3) were purified using a three-step protocol which includes ammonium sulfate precipitation, adsorption chromatography on phenyl sepharose and cationic exchange chromatography on SP sepharose. The molecular mass for SmaPrx2 and SmaPrx3
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