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WNT10B Antibody
Description
Research Area
Images & Validation
−| Tested Applications | IF, IHC, WB |
|---|---|
| Dilution range | WB: 1-500-2000 |
| Reactivity | Human, Rat |
Key Properties
−| Antibody Type | Primary Antibody |
|---|---|
| Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | Recombinant fusion protein of human WNT10B. The exact sequence is proprietary. |
| Purification | The antibody was purified by immunogen affinity chromatography. |
| Conjugation | Unconjugated |
Storage & Handling
−| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
|---|---|
| Form/Appearance | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
| Disclaimer | For research use only |
Alternative Names
−Similar Products
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62.5-4000 pg/mL
27.5 pg/mL
96 T, 48 TMouse Wingless Type MMTV Integration Site Family, Member 10B (WNT10B) ELISA Kit [orb781835]
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0.16-10 ng/mL
0.058 ng/mL
96 T, 48 TWNT10B Recombinant Mouse Monoclonal Antibody [orb1151991]
ICC, IF, IHC-Fr, IHC-P, WB
Mouse
Human, Rat
Mouse
Recombinant
Unconjugated
25 μl, 100 μl, 50 μl

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Western blot analysis of WNT10B expression in HeLa (A) whole cell lysates. (Predicted band size: 43 kD; Observed band size: 43 kD)

Immunohistochemical analysis of WNT10B staining in rat ovary 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 WNT10B staining in L929 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 AF594-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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Protocol Information
WNT10B Antibody (orb668652)
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