推荐产品
product name
Sepharose™ CL-2B 琼脂糖凝胶, Cross-linked
形狀
suspension
珠直徑
60-200 μm
孔徑
100,000-20,000,000 fractionation range (Dextrans)
70,000-40,000,000 fractionation range (Globular proteins)
儲存溫度
2-8°C
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一般說明
CL2B300-1L更新产品编号为 GE17-0140-01
應用
Sepharose™ CL-2B已被作为树脂用于：
- 凝胶渗透色谱 (GPC)
- 重力色谱
- 链霉亲和素亲和色谱
- 尺寸排阻色谱
琼脂糖 CL-2B 用于亲和层析、凝胶过滤层析、蛋白层析、分离介质和树脂。琼脂糖CL-2B 已用于研究卵巢癌和囊性纤维化。
法律資訊
Sepharose is a trademark of Cytiva
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）
102.2 °F - closed cup
閃點（°C）
39 °C - closed cup
Shyh-Dar Li et al.
Biochimica et biophysica acta, 1788(10), 2259-2266 (2009-07-15)
We have previously shown that the PEGylated LPD (liposome-polycation-DNA) nanoparticles were highly efficient in delivering siRNA to the tumor with low liver uptake. Its mechanism of evading the reticuloendothelial system (RES) is reported here. In LPD, nucleic acids were condensed
K Nakamura et al.
The Biochemical journal, 310 ( Pt 1), 263-269 (1995-08-15)
This study explores the role of cyclic nucleotides (i.e. cyclic AMP and cyclic GMP) in store-regulated external Ca2+ entry in human platelets. To stimulate store-regulated external Ca2+ entry, thapsigargin was used to deplete Ca2+ from the dense tubules, and sodium
R Bucki et al.
Biochemistry, 40(51), 15752-15761 (2001-12-19)
During platelet activation, phosphatidylserine (PS) exposure on the extracellular face of the plasma membrane is associated with increased procoagulant activity. PS externalization is generally attributed to an increase in intracellular Ca(2+). Various phospholipid transporters, such as specific scramblases or proteins
Extensive solubilization and depolymerization of cell wall polysaccharides during avocado (<I>Perseaamericana</I>) ripening involves concerted action of polygalacturonase and pectinmethylesterase.
Wakabayashi, K., et al.
Physiologia Plantarum, 108(4), 345-352 (2000)
H J Grimek et al.
Biology of reproduction, 30(2), 397-409 (1984-03-01)
Acetone precipitates of bovine follicular fluid from small (3-5 mm) and large (10-20 mm) follicles were fractionated by nondissociative procedures involving chromatography on Sephacryl S-300, DEAE cellulose, and Sepharose CL-2B. Most of the proteoglycan material eluted with a relatively low
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