Anti-Uroplakin III抗体[SFI-1] (ab78196)

ab78196 staining Uroplakin III in mouse bladder tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 1% BSA for 10 minutes at 21°C; antigen retrieval was by heat mediation in citric acid. Samples were incubated with primary antibody (1/600 in TBS/BSA/azide) for 16 hours at 21°C. A Biotin-conjugated goat anti-mouse IgG polyclonal (1/200) was used as the secondary antibody.

Positivity of only the lumenal cytoplasm of the Umbrella cells is clear.
As this is a mouse primary antibody, endogenous IgG will also be visualised in the interstitial spaces (red arrowheads), in Plasma cells (black arrowheads) and also in blood vessels if the animal has not been perfused-washed/fixed.

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ab78196 staining Uroplakin III in cow ureter tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 1% BSA for 10 minutes at 21°C; antigen retrieval was by heat mediation in citric acid. Samples were incubated with primary antibody (1/300 in TBS/BSA/azide) for 16 hours at 21°C. A Biotin-conjugated goat anti-mouse IgG polyclonal (1/200) was used as the secondary antibody.

Image shows clear, strong labelling of the lumenal membranes of the Umbrella cells.

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IHC-P image of Uroplakin-III staining on Marmoset bladder sections using ab78196 (1:400). The sections were deparaffinized and subjected to heat mediated antigen retrieval using citric acid. The sections were blocked using 1% BSA for 10 mins at 21°C. ab78196 was diluetd 1:400 and incubted with the sections for 2 hours at 21°C. The secondary antibody used was Goat polyclonal to anti mouse IgG conjugated to biotin (1:200)

IHC-P image of Uroplakin-III staining on Rat bladder sections using ab78196 (1:400). The sections were deparaffinized and subjected to heat mediated antigen retrieval using citric acid. The sections were blocked using 1% BSA for 10 mins at 21°C. ab78196 was diluetd 1:1000 and incubted with the sections for 2 hours at 21°C. The secondary antibody used was Goat polyclonal to anti mouse IgG conjugated to biotin (1:250)