Key features and details
- Goat polyclonal to TXNDC/TMX
- Suitable for: WB
- Reacts with: Human
- Isotype: IgG
Product nameAnti-TXNDC/TMX antibody
See all TXNDC/TMX primary antibodies
DescriptionGoat polyclonal to TXNDC/TMX
Tested applicationsSuitable for: WBmore details
Species reactivityReacts with: Human
- Human Liver lysates.
This product was previously labelled as TXNDC
Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Storage bufferpH: 7.30
Preservative: 0.02% Sodium azide
Constituents: 0.5% BSA, Tris buffered saline
Concentration information loading...
PurityImmunogen affinity purified
Purification notesPurified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Our Abpromise guarantee covers the use of ab37876 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||Use a concentration of 0.01 - 0.03 µg/ml. Predicted molecular weight: 32 kDa.
1 hour primary incubation is recommended for this product.
FunctionMay participate in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyze dithiol-disulfide exchange reactions.
Tissue specificityUbiquitous. Highly expressed in kidney, liver, placenta and lung.
Sequence similaritiesContains 1 thioredoxin domain.
Cellular localizationMembrane. Endoplasmic reticulum membrane. Predominantly found in the endoplasmic reticulum.
- Information by UniProt
- PDIA11 antibody
- Protein disulfide isomerase family A, member 11 antibody
- Thioredoxin domain containing 1 antibody
Anti-TXNDC/TMX antibody (ab37876) at 0.01 µg/ml + Human Liver lysate (35µg protein in RIPA buffer).
Developed using the ECL technique.
Predicted band size: 32 kDa
Observed band size: 35 kDa why is the actual band size different from the predicted?
Primary incubation was 1 hour.
ab37876 has not yet been referenced specifically in any publications.