偶联物
agarose conjugate
质量水平
形式
saline suspension
标记范围
≥5 mg per mL
技术
immunoprecipitation (IP): suitable
基质
cross-linked 4% beaded agarose
基质活化
cyanogen bromide
基质隔离区
1 atom
储存温度
2-8°C
一般描述
IgG是调节几种免疫应答的糖蛋白抗体。IgG-琼脂糖是一种免疫吸附剂,可用于纯化抗体,去除物种特异性交叉反应抗体,或从抗血清制剂中去除污染抗体。一般来说,可以使用相等树脂体积的IgG-琼脂糖从抗血清制剂中除去交叉反应抗体。然而,树脂与抗血清的比例将随个体应用而变化。免疫球蛋白G(IgG)是免疫球蛋白家族的一部分,并且是一种广泛表达的血清抗体。它的恒定(C)区域包含一条γ 重链。IgG的单体150kDa结构分别由两条相同的重链和两条相同的轻链组成,其分子量分别为50kDa和25kDa。该抗体的一级结构还含有二硫键,可用于连接两条重链、连接重链和轻链、以及链内的连接。IgG可进一步细分为四类,即具有不同重链(γ 1、γ 2、γ 3和γ 4)的IgG1、IgG2、IgG3和IgG4。
应用
兔IgG-琼脂糖已被用于免疫沉淀 和亲和纯化检测。
将与琼脂糖珠交联的兔IgG抗体(20 μl/ml)用于从293T细胞的全细胞提取物中分离RAT标记的蛋白。将交联至琼脂糖珠的兔IgG用于从哺乳动物全细胞提取物中纯化标记蛋白质(0.5至1.0mg总蛋白质结合至10 μl珠子上)。
外形
其悬浮于含有防腐剂的0.5M NaCl中。
其他说明
免责声明
除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
WGK
WGK 3
法规信息
动植物源性产品
Journal of genetics and genomics = Yi chuan xue bao, 44(2), 95-106 (2017-02-14)
In the sexually reproductive organisms, gametes are produced by meiosis following a limited mitotic amplification. However, the intrinsic program switching cells from mitotic to meiotic cycle is unclear. Alternative polyadenylation (APA) is a highly conserved means of gene regulation and
Molecular and cellular biology, 20(19), 7238-7246 (2000-09-13)
Putative RNA helicases are involved in most aspects of gene expression. All previously characterized members of the DEAH-box family of putative RNA helicases are involved in pre-mRNA splicing. Here we report the analysis of two novel DEAH-box RNA helicases, Dhr1p
RNA (New York, N.Y.), 14(10), 2061-2073 (2008-08-30)
Eukaryotic ribosome synthesis is a highly dynamic process that involves the transient association of scores of trans-acting factors to nascent pre-ribosomes. Many ribosome synthesis factors are nucleocytoplasmic shuttling proteins that engage the assembly pathway at early nucleolar stages and escort
Plant molecular biology, 55(1), 135-147 (2004-12-18)
Beyond the rewards of plant genome analysis and gene identification, characterisation of protein activities, post-translational modifications and protein complex composition remains a challenge for plant biologists. Ideally, methods should allow rapid isolation of proteins from plant material achieving a high
Molecular and cellular biology, 29(19), 5327-5338 (2009-07-29)
Before polyadenylated mRNA is exported from the nucleus, the 3'-end processing complex is removed by a poorly described mechanism. In this study, we asked whether factors involved in mRNP maturation and export are also required for disassembly of the cleavage
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门