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Merck

CL6B200

Sigma-Aldrich

Sepharose CL-6B Size Exclusion Resin

Cross-linked, 90-350 mesh

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About This Item

CAS号:
MDL號碼:
分類程式碼代碼:
23151817
NACRES:
NA.84

产品名称

Sepharose CL-6B, Cross-linked

品質等級

形狀

suspension

珠直徑

40-165 μm

孔徑

10,000-1,000,000 fractionation range (Dextrans)
10,000-4,000,000 fractionation range (Globular proteins)

儲存溫度

2-8°C

一般說明

琼脂糖CL是琼脂糖的交联衍生物,由琼脂糖与2,3-二溴丙醇在强碱性条件下反应制备。

應用

Sepharose CL-6B被用于亲和层析、蛋白质层析、凝胶过滤层析、分离介质和树脂。Sepharose CL-6B已可用于研究人黑色素瘤细胞的 体外 抑制以及收集其他有价值的抗癌研究数据。
琼脂糖CL-6B用于糖化酶和靶向核糖核蛋白(RNP)(RNP)的纯化。

法律資訊

Sepharose is a trademark of Cytiva

取代透過

产品编号
说明
价格

象形圖

Flame

訊號詞

Danger

危險聲明

危險分類

Flam. Liq. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3


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Hiroshi Tomoda et al.
Analytical biochemistry, 311(1), 50-56 (2002-11-21)
The galabiose structure Galalpha1-4Gal is rarely found in natural glycoproteins, but is abundantly present in pigeon egg white proteins as Galalpha(1-4)Galbeta(1-4)GlcNAc termini. Pigeon ovalbumin, ovomucoid, or the whole egg white were immobilized on periodate-oxidized Sepharose CL-6B gels by reductive amination.
Carla Cruz et al.
Journal of molecular recognition : JMR, 24(6), 975-980 (2011-11-01)
The binding between four matrices (beaded cellulose, cellulose acetate, cellulose triacetate and Sepharose CL-6B) and beaded cellulose derivatized with a thiacarbocyanine dye with 5'-mononucleotides is investigated by Saturation Transfer Difference Nuclear Magnetic Resonance (STD-NMR) technique. This procedure intends to identify
Mrinal Kumar Das et al.
International journal of biological macromolecules, 49(5), 1096-1103 (2011-09-21)
Articulatin-D, a 66 kDa ribosome inactivating protein (RIP) comprised of 29 kDa A-chain linked to 35 kDa B-chain, is purified from leafless mistletoe (Viscum articulatum) parasitic on Dalbergia sp. from Western Ghats (India). N-terminal sequence and LC-MS/MS analyses of A-
Preparation and Mammalian Plasma Membranes, 7 (1979)
N Vinay Kumar et al.
Methods (San Diego, Calif.), 32(4), 389-397 (2004-03-09)
Intracellular signaling by protein kinases controls many aspects of cellular biochemistry and physiology. Determining the direct substrates of protein kinases is important in understanding how these signaling enzymes exert their effect on cellular functions. One of the recent developments in

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