Uroplakin III Recombinant Rabbit Monoclonal Antibody [PD00-09]
cat.: HA721161
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human |
| Applications: | IHC-P, FC |
| Clonality: | Monoclonal |
| Clone number: | PD00-09 |
| Form: | Liquid |
| Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
| Storage buffer: | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | Predicted band size: 31 kDa |
| Isotype: | IgG |
| Immunogen: | Synthetic peptide within Human Uroplakin III aa 250 to the C-terminus. |
| Positive control: | Human bladder carcinoma tissue, Hela, 293. |
| Subcellular location: | Endoplasmic reticulum membrane. |
| Recommended Dilutions:
IHC-P FC |
1:5,000 1:500-1:1,000 |
| Uniprot #: | SwissProt: O75631 Human |
| Alternative names: | MGC119178 OTTHUMP00000028951 UP III UP3a UPIII UPIIIA UPK 3 UPK 3A UPK3 UPK3A UPK3A_HUMAN Uroplakin 3A Uroplakin III Uroplakin-3a Uroplakin3A UroplakinIII |
Images
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Fig1:
Immunohistochemical analysis of paraffin-embedded human bladder carcinoma tissue with Rabbit anti-Uroplakin III antibody (HA721161) at 1/5,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721161) at 1/5,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig2:
Flow cytometric analysis of Hela cells labeling Uroplakin III. Cells were fixed and permeabilized. Then stained with the primary antibody (HA721161, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |
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Fig3:
Flow cytometric analysis of 293 cells labeling Uroplakin III. Cells were fixed and permeabilized. Then stained with the primary antibody (HA721161, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.