j fibroblast marker cd26 Search Results


cd26 antibody  (NSJ Bioreagents)
99
NSJ Bioreagents cd26 antibody
Cd26 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
cd26 antibody - by Bioz Stars, 2026-03
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j fibroblast marker cd26  (Bio-Rad)
93
Bio-Rad j fibroblast marker cd26
Positive expression of <t>CD26</t> presented by flow cytometry with 940 nm diode laser. A Expression of CD26 at 1-week post-irradiation presenting percentages of differentiation in all experimental groups. The percentage of expression was higher in LB group at 1-week and B at 2-weeks post-irradiation and group L had the highest expression of CD26 marker compared to control group with no markers
J Fibroblast Marker Cd26, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse anti-cd-26  (Thermo Fisher)
90
Thermo Fisher mouse anti-cd-26
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Mouse Anti Cd 26, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
mouse anti-cd-26 - by Bioz Stars, 2026-03
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mf-cd-26  (Metglas Inc)
90
Metglas Inc mf-cd-26
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Mf Cd 26, supplied by Metglas Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mf-cd-26/product/Metglas Inc
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mf-cd-26 - by Bioz Stars, 2026-03
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mf cd 26  (MicroChem corp)
86
MicroChem corp mf cd 26
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Mf Cd 26, supplied by MicroChem corp, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mf cd 26 - by Bioz Stars, 2026-03
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mf cd-26  (Rohm and Haas)
90
Rohm and Haas mf cd-26
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Mf Cd 26, supplied by Rohm and Haas, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mf cd-26/product/Rohm and Haas
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mf cd-26 (0.26 n tmah) developer  (DuPont de Nemours)
90
DuPont de Nemours mf cd-26 (0.26 n tmah) developer
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Mf Cd 26 (0.26 N Tmah) Developer, supplied by DuPont de Nemours, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
mf cd-26 (0.26 n tmah) developer - by Bioz Stars, 2026-03
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dow microposit mf cd-26 developer  (MicroChemicals GmbH)
90
MicroChemicals GmbH dow microposit mf cd-26 developer
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Dow Microposit Mf Cd 26 Developer, supplied by MicroChemicals GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/dow microposit mf cd-26 developer/product/MicroChemicals GmbH
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dow microposit mf cd-26 developer - by Bioz Stars, 2026-03
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mf-cd-26  (Dow Chemical)
90
Dow Chemical mf-cd-26
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Mf Cd 26, supplied by Dow Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mf-cd-26/product/Dow Chemical
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microposit mf cd-26 developer  (Rohm and Haas)
90
Rohm and Haas microposit mf cd-26 developer
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Microposit Mf Cd 26 Developer, supplied by Rohm and Haas, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cd2.6d79  (DeLano Scientific)
90
DeLano Scientific cd2.6d79
Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.
Cd2.6d79, supplied by DeLano Scientific, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Positive expression of CD26 presented by flow cytometry with 940 nm diode laser. A Expression of CD26 at 1-week post-irradiation presenting percentages of differentiation in all experimental groups. The percentage of expression was higher in LB group at 1-week and B at 2-weeks post-irradiation and group L had the highest expression of CD26 marker compared to control group with no markers

Journal: BMC Biotechnology

Article Title: 940 nm diode laser induced differentiation of human adipose derived stem cells to temporomandibular joint disc cells

doi: 10.1186/s12896-022-00754-6

Figure Lengend Snippet: Positive expression of CD26 presented by flow cytometry with 940 nm diode laser. A Expression of CD26 at 1-week post-irradiation presenting percentages of differentiation in all experimental groups. The percentage of expression was higher in LB group at 1-week and B at 2-weeks post-irradiation and group L had the highest expression of CD26 marker compared to control group with no markers

Article Snippet: Based on the preliminary experimental results from above, the percentage differentiation of ADSCs into fibroblasts and chondrocytes at 1- and 2-weeks was observed post- irradiation with 940 nm diode laser at 5 J. Fibroblast marker CD26 (clone M-A261, mouse anti human, Bio Rad Laboratories (Pty) Ltd, South Africa) and chondrocyte marker CD49C (clone P1B5, mouse anti human, Bio Rad Laboratories (Pty) Ltd, South Africa) were used to confirm differentiation in all the experimental groups.

Techniques: Expressing, Flow Cytometry, Irradiation, Marker, Control

Flow cytometry results of experimental groups

Journal: BMC Biotechnology

Article Title: 940 nm diode laser induced differentiation of human adipose derived stem cells to temporomandibular joint disc cells

doi: 10.1186/s12896-022-00754-6

Figure Lengend Snippet: Flow cytometry results of experimental groups

Article Snippet: Based on the preliminary experimental results from above, the percentage differentiation of ADSCs into fibroblasts and chondrocytes at 1- and 2-weeks was observed post- irradiation with 940 nm diode laser at 5 J. Fibroblast marker CD26 (clone M-A261, mouse anti human, Bio Rad Laboratories (Pty) Ltd, South Africa) and chondrocyte marker CD49C (clone P1B5, mouse anti human, Bio Rad Laboratories (Pty) Ltd, South Africa) were used to confirm differentiation in all the experimental groups.

Techniques: Flow Cytometry, Cytometry

Differentiation of ADSCs to fibroblasts with 940 nm diode laser confirmed through immunofluorescent microscopic images. The differentiation of ADSCs to fibroblasts in group L at 1-week ( A ) and 2 weeks ( B ) post-irradiation presented as a green fluorescence (FITC) represents the expression of CD26. The nuclear counterstaining DAPI is represented in blue colour. The fluorescence and expression of marker on treated ( A and B ) cells are compared to untreated control ADSCs with no signs of differentiation

Journal: BMC Biotechnology

Article Title: 940 nm diode laser induced differentiation of human adipose derived stem cells to temporomandibular joint disc cells

doi: 10.1186/s12896-022-00754-6

Figure Lengend Snippet: Differentiation of ADSCs to fibroblasts with 940 nm diode laser confirmed through immunofluorescent microscopic images. The differentiation of ADSCs to fibroblasts in group L at 1-week ( A ) and 2 weeks ( B ) post-irradiation presented as a green fluorescence (FITC) represents the expression of CD26. The nuclear counterstaining DAPI is represented in blue colour. The fluorescence and expression of marker on treated ( A and B ) cells are compared to untreated control ADSCs with no signs of differentiation

Article Snippet: Based on the preliminary experimental results from above, the percentage differentiation of ADSCs into fibroblasts and chondrocytes at 1- and 2-weeks was observed post- irradiation with 940 nm diode laser at 5 J. Fibroblast marker CD26 (clone M-A261, mouse anti human, Bio Rad Laboratories (Pty) Ltd, South Africa) and chondrocyte marker CD49C (clone P1B5, mouse anti human, Bio Rad Laboratories (Pty) Ltd, South Africa) were used to confirm differentiation in all the experimental groups.

Techniques: Irradiation, Fluorescence, Expressing, Marker, Control

Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.

Journal: American Journal of Physiology - Renal Physiology

Article Title: The rat kidney contains high levels of prouroguanylin (the uroguanylin precursor) but does not express GC-C (the enteric uroguanylin receptor)

doi: 10.1152/ajprenal.00282.2010

Figure Lengend Snippet: Additional features of proUgn immunostaining in kidney. A: immunoperoxidase-stained tubule labeled with antibody 6910, viewed with differential interference contrast optics. The brown reaction product is restricted to the cytoplasm of the epithelial cells that form the tubule. The nuclei of the labeled cells are in close proximity to the apical membrane. B: immunoperoxidase-stained section labeled with antibody 6910 and lightly counterstained with hematoxylin to reveal cellular features. Immunoreactive tubules are light brown, while immunonegative tubules are gray-blue. As in B, the reaction product is intracellular, and the immunopositive cells have apically oriented nuclei. C: superimposed double-label fluorescence images of kidney cortex stained with anti-proUgn antibody 6910 (blue) and anti-CD 26 antibody (red). D and E: superimposed fluorescence images of kidney cortex showing autofluorescence (green) and proUgn-like immunoreactivity (blue) as detected by anti-proUgn antibody 6910 (D) or anti-proUgn antibody 6911 (E). Peanut agglutinin (PNA) binding (F), autofluorescence (G), and proUgn-like immunoreactivity (H) are shown in a section of kidney cortex. I: superimposed images F–H. Aquaporin-2 (AQP2)-like immunoreactivity (J), autofluorescence (K), and proUgn-like immunoreactivity (L) are shown in a section of kidney cortex. M: superimposed images J–L. Scale bars = 10 μm (A), 30 μm (B–E), and 50 μm (F–M). Asterisks mark unstained glomeruli.

Article Snippet: Sections were incubated overnight at 4°C with pairs of the following reagents: a 1:50 dilution of mouse anti-CD-26 (dipeptidyl peptidase-4; DPP-IV, Thermo Scientific), a 1:1,000 dilution of rabbit anti-proUgn antibody 6910 or 6911 (raised in-house), a 1:100 dilution of goat anti-aquaporin-2 (Santa Cruz Biotechnology, Santa Cruz, CA), or a 1.66 μg/ml solution of Alexa 658-conjugated peanut agglutinin (PNA; Invitrogen).

Techniques: Immunostaining, Staining, Labeling, Fluorescence, Binding Assay