Product nameAnti-GST antibody (TRITC)
See all GST primary antibodies
DescriptionGoat polyclonal to GST (TRITC)
ConjugationTRITC. Ex: 547nm, Em: 572nm
SpecificityThis antibody recognizes both purified and partially purified GST.
Tested applicationsSuitable for: Flow Cyt, Immunomicroscopymore details
Species reactivityReacts with: Species independent
Full length protein: GST from Schistosoma japonicum.
Label: Tetramethylrhodamine isothiocyanate (TRITC) (Molecular Weight 444 daltons). Absorption Wavelength: 550 nm. Emission Wavelength: 570 nm. Fluorochrome/Protein Ratio: 2.8 moles TRITC per mole of Goat IgG.
Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Storage bufferpH: 7.20
Preservative: 0.01% Sodium azide
Constituents: 1% BSA, 0.42% Potassium phosphate, 0.87% Sodium chloride
Concentration information loading...
PurityImmunogen affinity purified
Purification notesThis antibody was prepared from monospecific antiserum by immunoaffinity chromatography using GST coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities and extensive dialysis against the buffer stated above.
Our Abpromise guarantee covers the use of ab34713 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IM: Use at an assay dependent dilution.
This antibody is also suitable for fluorescent assays requiring lot to lot consistency.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
RelevanceGST (Glutathione S-Transferase) is a 26kDa protein encoded by the parasitic helminth Schistosoma japonicum and widely used in the pGEX family of GST plasmid expression vectors as a fusion protein with foreign proteins.
- Glutathione S Transferase antibody
- Glutathione S-transferase class-mu 26 kDa isozyme antibody
- GST antibody
ab34713 has not yet been referenced specifically in any publications.