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Merck

CCF100

Sigma-Aldrich

CM 琼脂糖凝胶

Fast Flow

别名:

羧甲基琼脂糖

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About This Item

CAS号:
MDL號碼:
分類程式碼代碼:
47101511
NACRES:
NA.56

品質等級

形狀

suspension

技術

affinity chromatography: suitable

基質

6% cross-linked agarose

粒徑

45-165 μm (wet bead)

孔徑

4,000,000 exclusion limit (av. mol. wt.)

pH值

4—13

容量

90-130 μeq/mL(gel basis)

儲存溫度

2-8°C

一般說明

Preswollen 溶于 20% 乙醇
CCF100-50 mL 更新的产品编号为 GE17-0719-01
GE17-0719-10 为 25 ml。

應用

CM 琼脂糖凝胶用于亲和层析、蛋白层析和离子交换层析。CM 琼脂糖凝胶已被用于研究膳食补充剂和表征蝰蛇毒液的生化和酶学属性。

法律資訊

Sepharose is a trademark of Cytiva

取代透過

象形圖

Flame

訊號詞

Warning

危險聲明

危險分類

Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

100.4 - 109.4 °F

閃點(°C)

38 - 43 °C

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Fei Wang et al.
Methods (San Diego, Calif.), 53(3), 208-213 (2010-12-24)
The infectivity associated with prion disease sets it apart from a large group of late-onset neurodegenerative disorders that shares the characteristics of protein aggregation and neurodegeneration. The unconventional infectious agent, PrP(Sc), is an aberrantly folded form of the normal prion
Biochemical and enzymatic characterization of BpMP-I, a fibrinogenolytic metalloproteinase isolated from Bothropoides pauloensis snake venom.
Naves de Souza, D.L., et al.
Comp. Biochem. Physiol., B: Comp. Biochem., 161, 102-109 (2012)
Balsamin, a novel ribosome-inactivating protein from the seeds of Balsam apple Momordica balsamina.
Kaur, I., et al.
Amino Acids (2011)
Tuo Wang et al.
Plant physiology, 172(4), 2107-2119 (2016-10-13)
The wall-loosening actions of β-expansins are known primarily from studies of EXPB1 extracted from maize (Zea mays) pollen. EXPB1 selectively loosens cell walls (CWs) of grasses, but its specific binding target is unknown. We characterized EXPB1 binding to sequentially extracted
Meifang Xiao et al.
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 36(11), 1065-1070 (2011-12-16)
To purify and identify HMGB1 secreted by liver cells HepG2 and immune cells U937. We cultured the liver cell lines HepG2 and immune cell lines U937, and stimulated them with HMGB1 (400 ng/mL) for 20 h. Then the supernatant was

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