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Merck
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主要文件

MAB5310

Sigma-Aldrich

Anti-Glutathione Antibody, clone D8

clone D8, Chemicon®, from mouse

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About This Item

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物来源

mouse

质量水平

抗体形式

affinity purified immunoglobulin

抗体产品类型

primary antibodies

克隆

D8, monoclonal

种属反应性

eukaryotes

制造商/商品名称

Chemicon®

技术

western blot: suitable

同位素/亚型

IgG2a

运输

dry ice

靶向翻译后修饰

unmodified

特异性

Reacts with reduced or non-reduced glutathione on proteins only. Does not react with free glutathione.

免疫原

Glutathione-protein complexes.

应用

Anti-Glutathione Antibody, clone D8 is an antibody against Glutathione for use in WB.
Research Category
Neuroscience
Research Sub Category
Oxidative Stress
Western blotting of glutatione conjugated proteins under non-reduced conditions: 1:500-1:1000; does not react with glutatione by itself.

Immunocytochemistry: 1:500-1:1000 (Non-reducing conditions)

Optimal working dilutions must be determined by end user.

外形

Format: Purified
Immunoglobulin purified by protein A affinity and presented as a liquid in PBS, pH 7.2 with 0.01% sodium azide.

储存及稳定性

Maintain at 2-8°C in undiluted aliquots for up to 6 months from date of receipt.

法律信息

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

12 - Non Combustible Liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Glutathione S-transferases interact with AMP-activated protein kinase: evidence for S-glutathionylation and activation in vitro.
Klaus, A; Zorman, S; Berthier, A; Polge, C; Ramirez, S; Michelland, S; Seve, M; Vertommen et al.
Testing null
Vladimir Alexandrovich Mitkevich et al.
Frontiers in pharmacology, 10, 922-922 (2019-09-03)
Exogenous RNases are selectively toxic to tumor cells. The reasons for this selectivity are not quite clear and should be searched for in the properties that distinguish malignant from normal cells. During onco-transformation, cells acquire properties allowing them to adapt
Tatiana A Seregina et al.
International journal of molecular sciences, 24(22) (2023-11-25)
Inactivation of enzymes responsible for biosynthesis of the cell wall component of ADP-glycero-manno-heptose causes the development of oxidative stress and sensitivity of bacteria to antibiotics of a hydrophobic nature. The metabolic precursor of ADP-heptose is sedoheptulose-7-phosphate (S7P), an intermediate of
Omid Azimzadeh et al.
Cancers, 15(13) (2023-07-14)
Recent epidemiologic studies support an association between chronic low-dose radiation exposure and the development of cardiovascular disease (CVD). The molecular mechanisms underlying the adverse effect of chronic low dose exposure are not fully understood. To address this issue, we have
Yugo Tsuchiya et al.
The Biochemical journal, 474(14), 2489-2508 (2017-03-28)
Coenzyme A (CoA) is an obligatory cofactor in all branches of life. CoA and its derivatives are involved in major metabolic pathways, allosteric interactions and the regulation of gene expression. Abnormal biosynthesis and homeostasis of CoA and its derivatives have

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