UBA1 Rabbit Polyclonal Antibody
WB | 1:500 - 1:2000 |
IHC | 1:50 - 1:200 |
IF/ICC | 1:50 - 1:200 |
Description | Rabbit polyclonal antibody to UBA1 |
Specificity | Recognizes endogenous levels of UBA1 protein. |
Antibody Type | Primary antibody |
Imnunogen | Recombinant fusion protein of human UBA1 |
Purification | The antibody was purified by immunogen affinity chromatography. |
Molecular Weight | Predicted: 113; Observed: 121 kD |
Form/Buffer | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
Alternative Names | A1S9T; UBE1; Ubiquitin-like modifier-activating enzyme 1; Protein A1S9; Ubiquitin-activating enzyme E1 |
Gene Symbol | UBA1 |
Entrez Gene | 7317(Human); 22201(Mouse); 314432(Rat) |
SwissProt | P22314(Human); Q02053(Mouse); Q5U300(Rat) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of UBA1 expression in U251 (A), rat spleen (B) whole cell lysates. (Predicted band size: 113; 117 kD; Observed band size: 121 kD)

Immunohistochemical analysis of UBA1 staining in rat liver formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunofluorescent analysis of UBA1 staining in HeLa cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a AREX® Fluor 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
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