P2459
Phenyl-Sepharose 6 Fast Flow
high substitution, extent of labeling: ~40 μmol per mL (high substitution)
Synonym(s):
Phenyl-Agarose
form
suspension
extent of labeling
~40 μmol per mL (high substitution)
matrix
agarose, 6% cross-linked
matrix activation
epichlorohydrin
matrix attachment
ether
matrix spacer
3 atoms
particle size
45-165 μm
storage temp.
2-8°C
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General description
P2459-200ML′s updated product is GE17-0973-05
Application
Phenyl 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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
104.0 °F
Flash Point(C)
40 °C
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Ronald P de Vries et al.
The Biochemical journal, 363(Pt 2), 377-386 (2002-04-05)
The faeB gene encoding a second feruloyl esterase from Aspergillus niger has been cloned and characterized. It consists of an open reading frame of 1644 bp containing one intron. The gene encodes a protein of 521 amino acids that has
<I>Candidaguilliermondii</I> grows on rare pentoses ? implications for production of pure xylitol.
Granstrom, T., et al.
Biotechnology Letters, 24, 507-510 (2002)
Frank J Ruzicka et al.
Biochimica et biophysica acta, 1774(2), 286-296 (2007-01-16)
A gene eam in Clostridium difficile encodes a protein that is homologous to lysine 2,3-aminomutase (LAM) in many other species but does not have the lysyl-binding residues Asp293 and Asp330 in LAM from Clostridium subterminale SB4. The C. difficile protein
Dawei Chen et al.
Biochemistry, 45(42), 12647-12653 (2006-10-18)
Lysine 2,3-aminomutase (LAM) from Clostridium subterminale SB4 catalyzes the interconversion of (S)-lysine and (S)-beta-lysine by a radical mechanism involving coenzymatic actions of S-adenosylmethionine (SAM), a [4Fe-4S] cluster, and pyridoxal 5'-phosphate (PLP). The enzyme contains a number of conserved acidic residues
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
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