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Key Documents

P3296

Millipore

蛋白G琼脂糖凝胶,快速流动

recombinant, expressed in E. coli, aqueous ethanol suspension

同義詞:

蛋白G琼脂糖,快速流动 来源于链球菌

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About This Item

MDL號碼:
分類程式碼代碼:
41106500
NACRES:
NA.56

重組細胞

expressed in E. coli

品質等級

形狀

aqueous ethanol suspension

分析物化學類別

proteins (Immunoglobulins of various mammalian species)

標籤範圍

~2 mg per mL

技術

affinity chromatography: suitable

基質

Sepharose 4B Fast Flow

基質活化

cyanogen bromide

基質結合

amino

基質墊片

1 atom

儲存溫度

2-8°C

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一般說明

蛋白G是从G组链球菌菌株G-148中分离得到的细菌胞壁蛋白,它能与免疫球蛋白(IgG)结合。通过木瓜蛋白酶消化从细胞中提取该蛋白,并依次使用DEAE-Sephadex离子交换层析、琼脂糖凝胶偶联人IgG亲和层析以及Sephadex G-200凝胶层析进行纯化。蛋白G与各种多克隆和单克隆IgG结合的pH条件基本在2.8-10之间,在pH 4-5时结合最强,在pH 10时结合最弱。它是强大的IgG检测试剂。
蛋白G是从G组链球菌菌株G-148中分离得到的细菌胞壁蛋白,它能与免疫球蛋白(IgG)结合。通过木瓜蛋白酶消化从细胞中提取该蛋白,并依次使用DEAE-Sephadex离子交换层析、琼脂糖凝胶偶联人IgG亲和层析以及Sephadex G-200凝胶层析进行纯化。蛋白G与各种多克隆和单克隆IgG结合的pH条件基本在2.8-10之间,在pH 4-5时结合最强,在pH 10时结合最弱。它是强大的IgG检测试剂。

P3296-5Ml的最新产品编号为GE17-0618-01

應用

蛋白G琼脂糖凝胶 被用于亲和层析,蛋白质层析,抗体纯化和表征,免疫亲和基质,蛋白A、G和L树脂,蛋白质相互作用以及纯化和检测。蛋白G琼脂糖凝胶 已被用于开发一种可确认人血清中是否存在抗促红细胞生成素中和抗体的方法,以及比较马血清中白蛋白和IgG消耗的方法。

外觀

悬浮于20%乙醇中

準備報告

使用重组链球菌蛋白G制备,其中白蛋白结合区已被移除

法律資訊

Sepharose is a trademark of Cytiva

象形圖

Flame

訊號詞

Warning

危險聲明

危險分類

Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

115.0 °F - closed cup

閃點(°C)

46.1 °C - closed cup


分析證明 (COA)

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Elena Kotova et al.
PLoS genetics, 5(2), e1000387-e1000387 (2009-02-21)
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Cordula M Stover et al.
Journal of immunology (Baltimore, Md. : 1950), 180(5), 3313-3318 (2008-02-23)
Properdin is a positive regulator of complement activation so far known to be instrumental in the survival of infections with certain serotypes of Neisseria meningitidis. We have generated a fully backcrossed properdin-deficient mouse line by conventional gene-specific targeting. In vitro
Cristina Hidalgo-Carcedo et al.
Nature cell biology, 13(1), 49-58 (2010-12-21)
Collective cell migration occurs in a range of contexts: cancer cells frequently invade in cohorts while retaining cell-cell junctions. Here we show that collective invasion by cancer cells depends on decreasing actomyosin contractility at sites of cell-cell contact. When actomyosin
Debby Kruijsen et al.
Journal of immunology (Baltimore, Md. : 1950), 185(11), 6489-6498 (2010-10-26)
Following infection with respiratory syncytial virus (RSV), reinfection in healthy individuals is common and presumably due to ineffective memory T cell responses. In peripheral blood of healthy adults, a higher CD4(+)/CD8(+) memory T cell ratio was observed compared with the
Aaron Pinnola et al.
The Journal of biological chemistry, 282(44), 32511-32519 (2007-09-11)
Poly(ADP-ribose) polymerase 1 protein (PARP1) mediates chromatin loosening and activates the transcription of inducible genes, but the mechanism of PARP1 regulation in chromatin is poorly understood. We have found that PARP1 interaction with chromatin is dynamic and that PARP1 is

條款

To determine the molecular weights of protein antigens, to study protein/protein interactions, to determine specific enzymatic activity, to monitor protein post-translational modifications and to determine the presence and quantity of proteins.

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