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Merck

SAB4200237

Anti-Glutathione-S-transferase (GST) antibody, Mouse monoclonal

clone 2H3-D10, purified from hybridoma cell culture

Synonyme(s) :

Mouse Anti-GST Tag

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A propos de cet article

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
Conjugate:
unconjugated
Clone:
2H3-D10, monoclonal
Application:
WB
Citations:
22
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biological source

mouse

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

2H3-D10, monoclonal

form

buffered aqueous solution

concentration

~1.0 mg/mL

technique(s)

western blot: 0.2-0.4 μg/mL using detection limit for GST-fustion protein is ∼ 10ng/lane

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

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General description

Anti-Glutathione-S-transferase (GST) antibody, mouse monoclonal, (mouse IgG1 isotype) is derived from the hybridoma 2H3-D10 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a GST-fusion protein. GST is a Phase II metabolic enzyme, expressed ubiquitously in both eukaryotes and prokaryotes. GSTs are classified in to three types based on their cellular localization, namely cytosolic GSTs, mitochondrial GSTs and microsomal GSTs.

Immunogen

hybridoma 2H3-D10 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a GST-fusion protein

Application

Anti-Glutathione-S-transferase (GST) antibody, Mouse monoclonal has been used in immunoblotting.

Biochem/physiol Actions

Glutathione-S-Transferase (GST) is an enzyme, which catalyzes the reaction of glutathione with a wide range of electrophilic substrates and therefore, plays a role in the detoxification of potential alkylating agents.(5) GST protects the cell against oxidative stress and several toxic molecules. It facilitates the synthesis and modification of leukotrienes and prostaglandins. GST from Schistosoma japonicum, has been cloned in several expression vectors as a 27.5 kDa molecule and used as a tag for expressing proteins of interest. These proteins are thus expressed as GST-fusion proteins. Antibodies to GST are useful in identifying the successful expression of these fusion proteins.
Monoclonal Anti- Glutathione-S-transferase (GST) recognizes GST from Schistosoma japonicum in GSTfusion proteins.

Physical form

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

Preparation Note

Store at −20 °C. For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze at 20 °C in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

Disclaimer

Unless otherwise stated in our catalog, 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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Classe de stockage

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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Consulter la Bibliothèque de documents

HnRNPK/miR-223/FBXW7 feedback cascade promotes pancreatic cancer cell growth and invasion
De He CH, et al.
Testing, 8(12), 20165-20165 (2017)
Glutathione transferases: substrates, inihibitors and pro-drugs in cancer and neurodegenerative diseases
Allocati N, et al.
Oncogenesis, 7(1), 1-15 (2018)
Non-radioactive LATS in vitro Kinase Assay
Hong AW and Guan KL
Bio-protocol, 7, e2391-e2391 (2017)
Ariel Shepley-McTaggart et al.
Viruses, 13(2) (2021-03-07)
Filoviruses Ebola (EBOV) and Marburg (MARV) are devastating high-priority pathogens capable of causing explosive outbreaks with high human mortality rates. The matrix proteins of EBOV and MARV, as well as eVP40 and mVP40, respectively, are the key viral proteins that
Audrey W Hong et al.
Bio-protocol, 7(14) (2017-11-07)
This protocol describes a method to directly measure LATS activity by an in vitro kinase assay using YAP as a substrate.

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