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Merck

G7781

Anti-Glutathione-S-Transferase (GST) antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution

동의어(들):

Anti-Glutathione-S-Transferase, Anti GST Antibody - Anti-Glutathione-S-Transferase (GST) antibody produced in rabbit, Anti Gst Antibody, Anti-Gst Antibody, Gst Antibody, Anti-GST

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제품정보 (DICE 배송 시 비용 별도)

NACRES:
NA.46
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
dot blot
indirect ELISA
western blot
Technique(s):
dot blot: suitable
indirect ELISA: 1:10,000
western blot: 1:2,000 using lysates of induced Escherichia coli expressing GST
Citations:
192

주요 문서

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제품 이름

Anti-Glutathione-S-Transferase (GST) antibody produced in rabbit, IgG fraction of antiserum, buffered aqueous solution

biological source

rabbit

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

packaging

antibody small pack of 25 μL

technique(s)

dot blot: suitable
indirect ELISA: 1:10,000
western blot: 1:2,000 using lysates of induced Escherichia coli expressing GST

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

200

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관련 카테고리

Application

Anti-Glutathione-S-Transferase (GST) antibody produced in rabbit has been used in immunoblotting.

Biochem/physiol Actions

Glutathione-S-transferase (GST) catalyzes the detoxication of electrophiles by glutathione conjugation. This enzyme provides protection against oxidative stress and toxic foreign chemicals. Polymorphism in GST gene is associated with the development of asthma and cutaneous basal cell carcinoma.

Disclaimer

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.

General description

Anti-Glutathione-S-Transferase (GST) antibody produced in rabbit is specific for native as well as denatured-reduced forms of glutathione-S-transferase from Schistosoma japonicum. The soluble GST is encoded by eight different genes in humans namely, α, μ, θ, π, ζ, σ, κ and ω on chromosome 6, 1, 22, 11, 14, 4, not known and 10 respectively.
The antibody is specific for native as well as denatured-reduced forms of glutathione-S-transferase from Schistosoma japonicum. Anti-GST may be used in various immunoassays to identify the expression of GST fusion proteins.

Immunogen

recombinant GST from Schistosoma japonicum expressed in E. coli.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

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저장 등급

10 - Combustible liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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시험 성적서(COA)

Lot/Batch Number
0000515671
0000515671
0000483561
0000483561
0000458355

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Glutathione-S-transferase family of enzymes
Strange R, et al.
Mutation Research. Fundamental and Molecular Mechanisms of Mutagenesis, 482(1-2), 21-26 (2001)
Analysis of protein-ligand interactions by fluorescence polarization
Rossi AM and TaylorCW
Nature Protocols, 6(3), 365-365 (2011)
Glutathione S-transferase polymorphisms and their biological consequences
Hayes JD and Strange RC
Pharmacology, 61(3), 154-166 (2000)
A novel simple extracellular leucine-rich repeat (eLRR) domain protein from rice (OsLRR1) enters the endosomal pathway and interacts with the hypersensitive-induced reaction protein 1 (OsHIR1).
Zhou L, et al.
Plant, Cell and Environment, 32(12), 1804-1820 (2009)
Nina Schroeder et al.
Journal of virology, 86(9), 4868-4882 (2012-02-22)
Mature vaccinia virus (vaccinia MV) infects a broad range of animals in vivo and cell cultures in vitro; however, the cellular receptors that determine vaccinia MV tropism and entry pathways are poorly characterized. Here, we performed quantitative proteomic analyses of
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