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Merck
CN

S9514

Sigma-Aldrich

Superose® 12 制备级琼脂糖珠

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MDL编号:
UNSPSC代码:
23151817
NACRES:
NA.56
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表单

suspension

粒径

20-40 μm (wet)

孔径

1,000-300,000 Da fractionation range (globular proteins)

储存温度

2-8°C

应用

Superose® 12制备级用于蛋白层析、凝胶过滤层析和凝胶过滤介质。Superose® 12制备级已用于纯化和表征化脓放线菌的溶血素以及来自地中海蝰(沙漠棘蛇)的纤维蛋原白酶。Superose® 12制备级也用于分离和表征化脓放线菌的胞外蛋白酶。

外形

悬浮于20%乙醇中
水乙醇悬浮液

其他说明

高交联珠状琼脂糖

法律信息

Superose is a registered trademark of Cytiva

象形图

Flame

警示用语:

Warning

危险声明

危险分类

Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

100.4 - 109.4 °F

闪点(°C)

38 - 43 °C

法规信息

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分析证书(COA)

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A Gasmi et al.
Toxicon : official journal of the International Society on Toxinology, 29(7), 827-836 (1991-01-01)
A fibrinogenase from Vipera lebetina venom was isolated by gel filtration in a Superose 12 column prep grade HR 16/50 and by ion-exchange in a Mono Q HR 5/5 column. The purified enzyme, which was obtained with a yield of
Isolation and characterization of an extracellular protease of Actinomyces pyogenes
Schaufuss, P., et al.
Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten Und Hygiene. 1. Abt. Medizinisch-Hygienische Bakteriologie, Virusforschung und Parasitologie. Originale, 271, 452-459 (1989)
H Youn et al.
Biochimica et biophysica acta, 1388(2), 405-418 (1998-12-22)
Lipoamide dehydrogenase was purified around 22-fold relative to the crude extracts of Streptomyces seoulensis with an overall yield of 9. 5%. The enzyme was composed of two identical subunits with a molecular mass of 54 kDa and contained 1 mol
C Balestrieri et al.
European journal of biochemistry, 193(1), 183-187 (1990-10-05)
The finding of a powerful inhibitor of pectin methylesterase in ripe kiwi fruit is reported. The inhibitor was revealed to be a glycoprotein. It was purified to homogeneity and found to have a molecular mass of about 28 kDa, as
J Durner et al.
Plant physiology, 93(3), 1027-1031 (1990-07-01)
Acetolactate synthase (ALS, EC 4.1.3.18) has been extracted and partially purified from etiolated barley shoots (Hordeum vulgare L.). Multiple forms of this enzyme were separated by gel filtration and/or anion-exchange chromatography using fast protein liquid chromatography. It could be demonstrated

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This page provides information about performing an isolation of recombinant protein complexes with different pull-down assays with products from Cytiva.

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