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- Biogradetech
- 美国
- BGT-ANT-24703
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
查看datasheet
- 保质期：
1年
- 级别：
科研级别
- 库存：
100
- 供应商：
艾美捷科技
- 应用范围：
查看datasheet
- 抗体英文名：
Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) Antibody, APC Conjugate
- 抗体名：
Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) Antibody, APC Conjugate
Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) 抗体, APC偶联，Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) Antibody, APC Conjugate，
产品名称：Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) 抗体, APC偶联-Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) Antibody, APC Conjugate
产品货号：BGT-ANT-24703
产品规格：5x30ug
应用类型：Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) 抗体, APC偶联产品详情查看提供的产品datasheet。
Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) 抗体, APC偶联,Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) Antibody, APC Conjugate
Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) 抗体, APC偶联-Human ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) Antibody, APC ConjugateHuman ADP-ribosylation Factor-like Protein 2-Binding Protein (ARL2BP) 抗体, APC偶联产品保存方式查看提供的产品datasheet。
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文献和实验Assay for Protein Modification by Poly-ADP-Ribose In Vitro
-modification domain of PARP has been shown to be a primary acceptor site of poly-ADP ribose (pADPr), other DNA binding nuclear proteins are also modified by pADPr. It is �generally accepted that pADPr polymer is built upon the carboxyl side chain of specific
【原创】Protein A Sepharose 之进化篇。。。
[img][/img]Protein A 柱之进化 Protein A是一种金黄色葡萄球菌细胞壁蛋白质，能特异性地与人和哺乳动物抗体（主要是IgG）的Fc区结合。因而，将Protein A 与琼脂糖凝胶以一定的方式结合，可制备用于抗体纯化的亲和填料。 早期的Protein A柱结合的都是天然Protein A。天然Protein A由5个IgG结合域和其它未知功能的非Fc结合域组成，分子量约42KD，结构如图1所示。这种柱子对IgG的亲和能力很强，可以吸附大量的lgG。但同时，天然
Analysis of the Protein S Gene in Protein S Deficiency
Protein S (PS) is a 71-kDa vitamin K-dependent glycoprotein first identified in human plasma by DiScipio and colleagues in 1977 (1 ), a year after the discovery of the anticoagulant protein C (PC) (2 ,3 ). A few years later, Walker
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