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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
Galili antigen undecaose grafted on gel for affinity chromatography (Linker-GEL A)
- 库存：
100+
- 供应商：
上海维亦特生物科技有限公司
储存：冷藏2-8℃
来源：Synthesis
糖链结构：Galα1-3(Galβ1-4GlcNAcβ1-3)4Galβ1-4Glc-NAc-CH2-(1.4-Tz)-(CH2)2-EG3-NH-Gel
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文献和实验Purification of Antibodies Using Affinity Chromatography
activity of a molecule to bind to a substrate, hapten, or antigen. Principles of matrix selection, gel preparation, and coupling of ligands have been reviewed extensively by Ostrove (2 ). Antibody affinity chromatography has been employed to isolate
Purification of Sequence‐Specific DNA‐Binding Proteins by Affinity Chromatography
available CNBr?activated Sepharose, and a support protocol describes how to purify crude synthetic oligonucleotides by gel electrophoresis prior to preparation of the affinity resin. The second basic protocol outlines the affinity chromatography procedure
Nitrocellulose-Based Immunoaffinity Chromatography
The first step in the affinity purification of antibodies is usually the immobilization of the corresponding antigen to a solid-phase matrix. Generally, this immobilization is done using some chemically reactive gel material such as cyanogen
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