CL2B300
Sepharose™ CL-2B Size Exclusion Resin
Cross-linked, 70-230 mesh
产品名称
Sepharose™ CL-2B 琼脂糖凝胶, Cross-linked
form
suspension
bead diameter
60-200 μm
pore size
100,000-20,000,000 fractionation range (Dextrans)
70,000-40,000,000 fractionation range (Globular proteins)
storage temp.
2-8°C
Quality Level
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Application
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。
General description
CL2B300-1L更新产品编号为 GE17-0140-01
Legal Information
Sepharose is a trademark of Cytiva
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
102.2 °F - closed cup
flash_point_c
39 °C - closed cup
法规信息
危险化学品
此项目有
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
Kazuyuki Wakabayashi et al.
Journal of plant physiology, 160(6), 667-673 (2003-07-23)
Pectinmethylesterase (PME, EC 3.2.1.11) and polygalacturonase (PG, EC 3.2.1.15) are known to operate in tandem to degrade methylesterified polyuronides. In this study, PGs purified from tomato and avocado fruit were compared in terms of their capacity to hydrolyze water-soluble polyuronides
Biochemical Analysis of Dimethyl Suberimidate-crosslinked Yeast Nucleosomes
Ichiakwa Y and Kaufman PD
Bio-protocol, 8(6) (2018)
H Ceri et al.
American journal of respiratory cell and molecular biology, 5(1), 51-55 (1991-07-01)
Endogenous heparin-binding lectin purified from postmortem lung samples of two cystic fibrosis (CF) patients was compared to lectin derived from normal tissue with respect to structure, carbohydrate specificity, interaction with alginate derived from CF isolates of Pseudomonas aeruginosa, and secretion
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