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安全信息

G3907

Millipore

谷胱甘肽−琼脂糖

set of 3 pre-packed columns (2.5 ml each), (1:1 suspension in a 0.5 M NaCl + 20% ethanol solution)

别名:

GSH-琼脂糖, S-连接谷胱甘肽琼脂糖

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1 EA
¥12,173.40

¥12,173.40

预计发货时间2025年8月13日详情

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1 EA
¥12,173.40

About This Item

MDL编号:
MFCD00131200
UNSPSC代码:
41106500
NACRES:
NA.56

¥12,173.40

预计发货时间2025年8月13日详情

质量水平

200

表单

(1:1 suspension in a 0.5 M NaCl + 20% ethanol solution)

分析物化学类别

proteins (GST)

包装

set of 3 pre-packed columns (2.5 ml each)

技术

immunoprecipitation (IP): suitable
protein purification: suitable

基质

cross-linked 4% beaded agarose

储存温度

2-8°C

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Terrific Broth

LB Broth (Miller) Liquid microbial growth medium

L2542

LB Broth (Miller)

LB Broth (Miller) Highly-referenced nutrient-rich microbial growth powder medium, suitable for regular E.coli culture

L3522

LB Broth (Miller)

technique(s)

microbiological culture: suitable

technique(s)

microbiological culture: suitable

technique(s)

microbiological culture: suitable

technique(s)

-

form

liquid

form

powder

form

liquid

form

powder

sterility

sterile; 0.2 μm filtered

sterility

non-sterile

sterility

sterile; 0.2 μm filtered

sterility

non-sterile

application(s)

microbiology

application(s)

agriculture
food and beverages
microbiology

application(s)

microbiology

application(s)

food and beverages

Quality Level

500

Quality Level

200

Quality Level

400

Quality Level

200

一般描述

这些柱中的树脂由通过硫连接至环氧活化的4%交联琼脂糖珠上的谷胱甘肽组成，形成12个原子间隔基。 [1]

应用

利用谷胱甘肽-琼脂糖的亲和层析技术可以快速、温和、非变性和高度选择性地纯化谷胱甘肽结合酶，如谷胱甘肽-S-转移酶、谷胱甘肽过氧化物酶和乙二醛酶I。[2]
该产品用于新型色胺和四氢-β-咔啉基CDK4选择性抑制剂的设计、合成和生物学评价。[3]它还可用于研究Fascaplysin激发的二吲哚作为CDK4/细胞周期素D1的选择性抑制剂。[4]
利用谷胱甘肽-琼脂糖亲和层析技术，可以快速、温和、非变性和高度选择性地纯化含有谷胱甘肽结合序列的蛋白质，如谷胱甘肽S-转移酶(GST)、谷胱甘肽过氧化物酶和乙二醛酶I。

联系

产品悬浮液编号G 4510

外形

0.5 M NaCl + 20%乙醇溶液的混悬液（1:1）

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

180.1 °F

闪点(°C)

82.3 °C

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SLBR3849V
016K7056
074K7025

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F Toribio et al.
Journal of chromatography. B, Biomedical applications, 684(1-2), 77-97 (1996-09-20)
The different preparative techniques and related analytical methods used for purification of glutathione peroxidase, glutathione transferase and glutathione reductase, described in papers published in the last ten years, have been reviewed in this article. Among the different purification techniques, chromatography
Carine Aubry et al.
Bioorganic & medicinal chemistry, 17(16), 6073-6084 (2009-07-28)
We present the design, synthesis and biological activity of a new series of substituted 3-(2-(1H-indol-1-yl)ethyl)-1H-indoles and 1,2-di(1H-indol-1-yl)alkanes as selective inhibitors of CDK4/cyclin D1. The compounds were designed to explore the relationship between the connection mode of the indolyl moieties and
Dustin L Johnson et al.
Journal of bacteriology, 190(8), 2972-2980 (2008-02-19)
Chlamydophila pneumoniae is a gram-negative obligate intracellular bacterial pathogen that causes pneumonia and bronchitis and may contribute to atherosclerosis. The developmental cycle of C. pneumoniae includes a morphological transition from an infectious extracellular elementary body (EB) to a noninfectious intracellular
Paul R Jenkins et al.
Bioorganic & medicinal chemistry, 16(16), 7728-7739 (2008-07-25)
We present the design, synthesis and biological activity of a library of substituted (biphenylcarbonyl)-tryptamine and (biphenylcarbonyl)-tetrahydro-beta-carboline compounds related to the natural product fascaplysin, as novel inhibitors of CDK4/cyclin D1. We show all these molecules, prepared using the Suzuki-Miyaura reaction, being
Xiu Feng Hu et al.
The Journal of clinical investigation, 119(2), 362-375 (2009-01-17)
Provirus integration site for Moloney murine leukemia virus (PIM1) is a proto-oncogene that encodes a serine/threonine kinase with multiple cellular functions. Overexpression of PIM-1 plays a critical role in progression of prostatic and hematopoietic malignancies. Here we describe the generation
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蛋白质Pull-Down技术

利用亲和力、GST pull-down、TAP 和共免疫沉淀方法，通过Pull-Down研究体外蛋白质互作。

Protein Pull-Down Techniques

Investigate in vitro protein-protein interactions with pull-down assays, utilizing affinity, GST pull-down, TAP, and co-immunoprecipitation methods.

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