CL6B200
Sepharose™ CL-6B Size Exclusion Resin
Cross-linked, 90-350 mesh
产品名称
Sepharose™ CL-6B, Cross-linked
表单
suspension
珠子直径
40-165 μm
孔径
10,000-1,000,000 fractionation range (Dextrans)
10,000-4,000,000 fractionation range (Globular proteins)
储存温度
2-8°C
一般描述
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。
应用
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。
法律信息
Sepharose is a trademark of Cytiva
警示用语：
Danger
危险声明
危险分类
Flam. Liq. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 3
法规信息
危险化学品
此项目有
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.
D A Grahame
The Journal of biological chemistry, 266(33), 22227-22233 (1991-11-25)
An enzyme complex containing carbon monoxide dehydrogenase and a corrinoid protein has been isolated from Methanosarcina barkeri. Sodium dodecyl sulfate-gel electrophoresis revealed five polypeptides of molecular masses alpha = 19,700, beta = 84,500, gamma = 63,200, delta = 53,000, and
C C Chadwick et al.
Archives of biochemistry and biophysics, 252(2), 348-356 (1987-02-01)
As isolated by our recently developed large-scale procedure, the Neurospora plasma membrane H+-ATPase exists as a homogeneous, oligomeric complex of 105,000-Da monomers with a molecular mass equivalent to a spherical protein of about 1 million Da, as judged by its
Amylolytic fungi in starter cakes for rice beer production
Das AJ, et al.
The Journal of General and Applied Microbiology, 63(4), 236-245 (2017)
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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