P2334
Phenyl-Sepharose 6 Fast Flow
low substitution, extent of labeling: ~20 μmol per mL
Synonym(s):
Phenyl-Agarose
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About This Item
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Quality Level
form
suspension
extent of labeling
~20 μmol per mL
matrix
agarose, 6% crosslinked
matrix activation
epichlorohydrin
matrix attachment
ether
matrix spacer
3 atoms
particle size
45-165 μm
capacity
~14 mg/mL binding capacity (BSA)(lineal flow rate of 100 cm/hr)
storage temp.
2-8°C
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General description
P2334-200ml′s updated product number is GE17-0965-05
Application
Phenyl [YM="Sepharose"] is used in protein chromatography, affinity chromatography, hydrophobic interaction media, resins and separation media. Phenyl Sepharose™ has been used in studies that contributed to improving industrial applications in additives in detergents and feed industries. Phenyl sepharose has also been used to study microbial communities inhabiting hypersaline environments.
Physical form
Suspension in 20% ethanol
aqueous ethanol suspension
Legal Information
Sepharose is a trademark of Cytiva
replaced by
Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
95.0 °F
Flash Point(C)
35 °C
Certificates of Analysis (COA)
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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
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
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
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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