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Key Documents

P2334

Sigma-Aldrich

Phenyl-Sepharose 6 Fast Flow

low substitution, extent of labeling: ~20 μmol per mL

Synonym(e):

Phenyl-Agarose

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About This Item

MDL-Nummer:
MFCD00147908
UNSPSC-Code:
41106500
NACRES:
NA.56

Qualitätsniveau

100

Form

suspension

Kennzeichnungsgrad

~20 μmol per mL

Matrix

agarose, 6% crosslinked

Matrixaktivierung

epichlorohydrin

Matrixanbindung

ether

Matrix-Spacer

3 atoms

Partikelgröße

45-165 μm

Kapazität

~14 mg/mL binding capacity (BSA)(lineal flow rate of 100 cm/hr)

Lagertemp.

2-8°C

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Allgemeine Beschreibung

P2334-200ml′s updated product number is GE17-0965-05

Anwendung

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.

Physikalische Form

Suspension in 20% Ethanol
aqueous ethanol suspension

Rechtliche Hinweise

Sepharose is a trademark of Cytiva

Ersetzt durch

Produkt-Nr.
Beschreibung
Preisangaben

Piktogramme

Flame
GHS02

Signalwort

Warning

H-Sätze

H226

Gefahreneinstufungen

Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

95.0 °F

Flammpunkt (°C)

35 °C

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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DEAE–Sepharose™ Fast Flow

Sigma-Aldrich

DFF100

DEAE–Sepharose™

Q Sepharose™ Fast Flow Cytiva 17-0510-01, pack of 300 mL

GE17-0510-01

Q Sepharose™ Fast Flow

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
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
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
Simona Lobasso et al.
Photochemistry and photobiology, 88(3), 690-700 (2012-01-18)
We have isolated and characterized the light-driven proton pump Bop I from the ultrathin square archaeon Haloquadratum walsbyi, the most abundant component of the dense microbial community inhabiting hypersaline environments. The disruption of cells by hypo-osmotic shock yielded Bop I
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