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Merck
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重要文件

A2909

Sigma-Aldrich

兔IgG-琼脂糖

saline suspension

同義詞:

IgG agarose beads

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About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.46
暫時無法取得訂價和供貨情況

共軛

agarose conjugate

形狀

saline suspension

標籤範圍

≥5 mg per mL

技術

immunoprecipitation (IP): suitable

基質

cross-linked 4% beaded agarose

基質活化

cyanogen bromide

基質墊片

1 atom

儲存溫度

2-8°C

一般說明

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。[1]

應用

兔IgG-琼脂糖已被用于免疫沉淀[2] 和亲和纯化检测[3]
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)。

外觀

其悬浮于含有防腐剂的0.5M NaCl中。

免責聲明

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。

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3


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A Colley et al.
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
Emmanuel Vanrobays et al.
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
Lingjuan Shan et al.
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
Claus-Peter Witte et al.
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
Alison L Pidoux et al.
Molecular cell, 33(3), 299-311 (2009-02-17)
The mechanisms ensuring specific incorporation of CENP-A at centromeres are poorly understood. Mis16 and Mis18 are required for CENP-A localization at centromeres and form a complex that is conserved from fission yeast to human. Fission yeast sim1 mutants that alleviate

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