Key features and details
- Rabbit polyclonal to FUT11
- Suitable for: ICC/IF, IHC-P, WB
- Reacts with: Human
- Isotype: IgG
Product nameAnti-FUT11 antibody
DescriptionRabbit polyclonal to FUT11
Tested applicationsSuitable for: ICC/IF, IHC-P, WBmore details
Species reactivityReacts with: Human
antigen sequence, corresponding to C terminal amino acids 348-482 of Human FUT11.
- Human liver tissue; Transfected HEK293T Cell lysate.
Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Storage bufferpH: 7.20
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine)
Concentration information loading...
PurityImmunogen affinity purified
Our Abpromise guarantee covers the use of ab121411 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|ICC/IF||Use a concentration of 0.25 - 2 µg/ml.|
|IHC-P||1/50 - 1/200. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.|
|WB||1/250 - 1/500.|
PathwayProtein modification; protein glycosylation.
Sequence similaritiesBelongs to the glycosyltransferase 10 family.
Cellular localizationGolgi apparatus > Golgi stack membrane.
- Information by UniProt
- 3)-fucosyltransferase 11 antibody
- Alpha (1,3) fucosyltransferase 11 antibody
- Alpha-(1 antibody
Immunofluorescent staining of Human cell line A-431 shows positivity in nuclear membrane and golgi apparatus. Recommended concentration of ab121411 1-4 µg/ml. Cells treated with PFA/Triton X-100.
ab121411 at 1/50 dilution staining FUT11 in paraffin-embedded Human liver tissue by Immunohistochemistry.
All lanes : Anti-FUT11 antibody (ab121411) at 1/250 dilution
Lane 1 : Negative control (vector only transfected HEK293T lysate)
Lane 2 : FUT11-transfected HEK293T over-expression Lysate (Co-expressed with a C-terminal myc-DDK tag (~3.1 kDa))
Developed using the ECL technique.
ab121411 has not yet been referenced specifically in any publications.