目录产品 » 抗体产品 » 标签抗体 » THE™ GST Antibody, mAb, Mouse

THE™ GST Antibody, mAb, Mouse

THE™ Anti-GST Monoclonal Antibody (Mouse) recognizes GST localized at the C-terminal, N-terminal, and internal region of GST-tagged fusion proteins. 
¥1500
A00865

Specificity THE™ Anti-GST Monoclonal Antibody (Mouse) recognizes GST localized at the C-terminal, N-terminal, and internal region of GST-tagged fusion proteins. 
Host Species Mouse
Immunogen Recombinant GST protein (26 kDa)
Conjugate Unconjugated
返回

Working concentrations for specific applications should be determined by the investigator. The appropriate concentrations may be affected by secondary antibody affinity, antigen concentration, the sensitivity of the method of detection, temperature, the length of the incubations, and other factors. The suitability of this antibody for applications other than those listed below has not been determined. The following concentration ranges are recommended starting points for this product.
Application Recommended Usage
ELISA 0.05-0.2 µg/ml
Western Blot 0.1-1.0 µg/ml
Immunoprecipitation (IP) 1 µg/ml
返回

Form Lyophilized
Storage Buffer 1: 40 µg, 100 µg, 200 µg (GenScript, A00865), lyophilized with PBS, pH 7.4, containing 0.02% sodium azide.
2: 500 µg (GenScript, A00865), lyophilized with PBS, pH 7.4, without sodium azide or carrier protein. 
Reconstitution Reconstitute the lyophilized powder with deionized water (or equivalent) to a final concentration of 0.5 mg/mL. 
Storage Instructions The lyophilized product remains stable for up to 1 year at -20°C from the date of receipt. The reconstituted antibody can be stored for 2-3 weeks at 2-8°C. For long term storage, aliquot and store at -20°C or below. Avoid repeated freezing and thawing cycles.
Purification Protein A affinity column
Isotype Mouse IgG1,κ
Clonality Monoclonal
Clone ID 2F10B9
Note GenScript can offer this product per customer's request including product size, buffer components, etc.
返回

THE™ GST Antibody, MAb, Mouse

Figure 1. The affinity of THE™ GST Antibody, mAb, Mouse (GenScript, A00865) for C-terminal, N-terminal, and internal GST-tagged fusion proteins was analyzed by Western blotting.

Lane 1: N-terminal GST-tagged fusion protein
Lane 2: Internal GST-tagged fusion protein
Lane 3: C-terminal GST-tagged fusion protein

The primary antibody was THE™ GST Antibody, mAb, Mouse (GenScript, A00865) used at 1 μg/mL concentration. The secondary antibody was Goat Anti-Mouse IgG (H&L) [HRP] Polyclonal Antibody (GenScript, A00160, 1:20,000). »

<
>

Target Background Schistosoma japonicum glutathione S-transferase (GST) is a 26 kDa enzyme that conjugates reduced glutathione to hydrophobic electrophiles. GST is an ideal fusion partner for production of foreign proteins in commercially available expression systems because it can be expressed in high levels in E.coli. The fusion proteins can be purified to homogenity in a single step as the GST portion of the protein binds tightly to immobilized glutathione. Elution can be accomplished using free glutathione. The GST portion of the fusion protein can be separated from the protein of interest by using site-specific proteases. Antibodies directed against GST can be helpful in detecting the fusion protein during purification and to detect cleavage of GST from the protein of interest.
Synonyms Mouse Anti-GST monoclonal antibody
返回

For laboratory research use only. Direct human use, including taking orally and injection and clinical use are forbidden.


Peng Xu, et al. Blue light-dependent interactions of CRY1 with GID1 and DELLA proteins regulate gibberellin signaling and photomorphogenesis in Arabidopsis. The Plant cell. (2021-05)
Huiping Guo, et al. Molecular cloning and functional characterization of Physcomitrella patens UBC13-UEV1 genes required for Lys63-linked polyubiquitination. Plant Sci. (2020)
Guangwen Wang, et al. The G Protein-Coupled Receptor FFAR2 Promotes Internalization during Influenza A Virus Entry. J Virol. (2019-11)
NguyenKha The, et al. N-terminal methionine excision of proteins creates tertiary destabilizing N-degrons of the Arg/N-end rule pathway. J. Biol. Chem. (2019-03)
Zheng T, et al. Post-transcriptional regulation of Ghd7 protein stability by phytochrome and OsGI in photoperiodic control of flowering in rice. New Phytol. (2019)
Sadr KarimiShaghayegh, et al. Carbon nanotubes as molecular transporters to study a new mechanism for molecular entry into the cell nucleus using actin polymerization force. PLoS ONE. (2019)
Schultz-Larsen T, et al. The AMSH3 ESCRT-III-Associated Deubiquitinase Is Essential for Plant Immunity. Cell Rep. (2018)
ZhouJing, et al. Porcine Mx1 Protein Inhibits Classical Swine Fever Virus Replication by Targeting Nonstructural Protein NS5B. J. Virol. (2018)
PengBin, et al. Phosphorylation of LSD1 by PLK1 promotes its chromatin release during mitosis. Cell Biosci. (2017-01)
Shen J, et al. JMJD5 cleaves monomethylated histone H3 N-tail under DNA damaging stress. EMBO Rep. (2017)
PillaySirika, et al. AAV serotypes have distinctive interactions with domains of the cellular receptor AAVR. J. Virol. (2017)
Truebestein L, et al. A molecular ruler regulates cytoskeletal remodelling by the Rho kinases. Nat Commun. (2015-12)
PA DaRosa, et al. Allosteric activation of the RNF146 ubiquitin ligase by a poly (ADP-ribosyl) ation signal. Nature. (2014-10)
M Zhu, et al. HERC2/USP20 coordinates CHK1 activation by modulating CLASPIN stability. Nucleic Acids Res. (2014-10)
Zhao H, et al. BCL10 regulates RNF8/RNF168-mediated ubiquitination in the DNA damage response. Cell Cycle. (2014)
Tsai KL, et al. A conserved Mediator-CDK8 kinase module association regulates Mediator-RNA polymerase II interaction. Nat Struct Mol Biol. (2013-05)
Muzammel Haque and Konstantin G. Kousoulas., et al. The Kaposi's Sarcoma-Associated Herpesvirus ORF34 Protein Binds to HIF-1α and Causes Its Degradation via the Proteasome Pathway. J Virol. (2013-02)
Ghai R, et al. Structural basis for endosomal trafficking of diverse transmembrane cargos by PX-FERM proteins. Proc Natl Acad Sci U S A. (2013-02)
Chenere P. Ramsey, et al. Identification and characterization of a novel endogenous murine parkin mutation. J Neurochem. (2010-04)
查看更多
返回