P7892
Phenyl-Sepharose CL-4B
extent of labeling: ~40 μmol per mL
Sinônimo(s):
Phenyl-Agarose
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About This Item
Produtos recomendados
Formulário
suspension
Nível de qualidade
Extensão da rotulagem
~40 μmol per mL
Matriz
agarose, 4% cross-linked
ativação da matriz
epichlorohydrin
ligação da matriz
hydroxyl
espaçador de matriz
3 atoms
tamanho de partícula
45-165 μm
capacidade
15-20 mg/mL binding capacity (human serum albumin)
3-5 mg/mL binding capacity (β-lactoglobulin)
temperatura de armazenamento
2-8°C
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Descrição geral
P7892-200ML′s updated product number is GE17-0810-01
Aplicação
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.
forma física
Suspension in 20% ethanol
aqueous ethanol suspension
Informações legais
Sepharose is a trademark of Cytiva
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Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Flam. Liq. 3
Código de classe de armazenamento
3 - Flammable liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
96.8 °F
Ponto de fulgor (°C)
36 °C
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O Ploux et al.
The Biochemical journal, 283 ( Pt 2), 327-331 (1992-04-15)
The 8-amino-7-oxopelargonate synthase [6-carboxyhexanoyl-CoA:L-alanine carboxyhexanoyltransferase (decarboxylating); EC 2.3.1.47] from Bacillus sphaericus involved in biotin biosynthesis was purified from an Escherichia coli overproducing strain. The purification afforded an electrophoretically homogeneous enzyme with a specific activity of 0.67 unit/mg. The purified enzyme
Cui, W., et al.
Enzyme and Microbial Technology, 24(3-4), 200-208 (1999)
W Kroutil et al.
Journal of biotechnology, 61(2), 143-150 (1998-07-09)
A highly enantioselective, soluble epoxide from Nocardia sp. EH1 was purified to homogeneity via a four-step procedure: (i) hydrophobic interaction chromatography on Phenyl Sepharose CL-4B, (ii) anion exchange chromatography on SOURCE 30Q, followed by (iii) a second hydrophobic interaction chromatography
Sheref S Mansy et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(36), 13351-13355 (2008-09-05)
The earliest cells may have consisted of a self-replicating genetic polymer encapsulated within a self-replicating membrane vesicle. Here, we show that vesicles composed of simple single-chain amphiphiles such as fatty acids, fatty alcohols, and fatty-acid glycerol esters are extremely thermostable
Sheref S Mansy et al.
Nature, 454(7200), 122-125 (2008-06-06)
Contemporary phospholipid-based cell membranes are formidable barriers to the uptake of polar and charged molecules ranging from metal ions to complex nutrients. Modern cells therefore require sophisticated protein channels and pumps to mediate the exchange of molecules with their environment.
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