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Key Documents

P2334

Sigma-Aldrich

Phenyl-Sepharose 6 flujo rápido

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

Sinónimos:

Phenyl-Agarose

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About This Item

MDL number:
MFCD00147908
UNSPSC Code:
41106500
NACRES:
NA.56

Quality Level

100

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

Suspensión en 20% de etanol
aqueous ethanol suspension

Legal Information

Sepharose is a trademark of Cytiva

replaced by

Referencia del producto
Descripción
Precios

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

95.0 °F

flash_point_c

35 °C

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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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
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
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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