Product nameAnti-ESD antibody [EPR8446]
See all ESD primary antibodies
DescriptionRabbit monoclonal [EPR8446] to ESD
Tested applicationsSuitable for: WB, Flow Cytmore details
Unsuitable for: ICC,IHC-P or IP
Species reactivityReacts with: Human
Synthetic peptide from a region of Human ESD (P10768)
- K562, HeLa, Jurkat, Caco-2 cell lysates; Jurkat cells
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMab® patents.
This product is a recombinant rabbit monoclonal antibody.
Storage instructionsShipped at 4°C. Store at -20°C. Stable for 12 months at -20°C.
Storage bufferpH: 7.20
Preservative: 0.01% Sodium azide
Constituents: 9% PBS, 40% Glycerol, 0.05% BSA, 50% Tissue culture supernatant
PurityTissue culture supernatant
Our Abpromise guarantee covers the use of ab131211 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/1000 - 1/10000. Predicted molecular weight: 31 kDa.|
|Flow Cyt||1/10 - 1/100.
ab172730 - Rabbit monoclonal IgG, is suitable for use as an isotype control with this antibody.
FunctionSerine hydrolase involved in the detoxification of formaldehyde.
Sequence similaritiesBelongs to the esterase D family.
Cellular localizationCytoplasm. Cytoplasmic vesicle.
- Information by UniProt
- EC 22.214.171.124 antibody
- Es-10 antibody
- Es10 antibody
All lanes : Anti-ESD antibody [EPR8446] (ab131211) at 1/1000 dilution
Lane 1 : K562 cell lysate
Lane 2 : Jurkat cell lysate
Lane 3 : Caco-2 cell lysate
Lane 4 : HeLa cell lysate
Lysates/proteins at 10 µg per lane.
Predicted band size: 31 kDa
ab131211 at 1/10 labelling ESD in permeabilized Jurkat cells by flow cytometry. Rabbit IgG negative control is in green.
ab131211 has not yet been referenced specifically in any publications.