vectasheild mounting media Search Results


97
Vector Laboratories vectashield fluorescent mounting media
Vectashield Fluorescent Mounting Media, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories vectashield mounting media with dapi
Vectashield Mounting Media With Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories vectashield hardset mounting media with dapi
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
Vectashield Hardset Mounting Media With Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Vector Laboratories vectashield hardset antifade mounting media
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
Vectashield Hardset Antifade Mounting Media, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories vectashield vibrance mounting media with dapi
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
Vectashield Vibrance Mounting Media With Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Vector Laboratories vectashield
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
Vectashield, supplied by Vector Laboratories, 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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96
Vector Laboratories vectashield vibrance antifade mounting media
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
Vectashield Vibrance Antifade Mounting Media, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories 4 6 diamidino 2phenylindole dapi nuclear stain
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
4 6 Diamidino 2phenylindole Dapi Nuclear Stain, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories dapi
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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AbCys s a dapi mounting media
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
Dapi Mounting Media, supplied by AbCys s a, 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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86
Vector Laboratories 4 6 diamidino 2 phenylindole dapi stain
Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and <t>DAPI</t> (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.
4 6 Diamidino 2 Phenylindole Dapi Stain, supplied by Vector Laboratories, 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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Image Search Results


Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and DAPI (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.

Journal: Journal of cell science

Article Title: Loss of Ca 2+ entry via Orai-TRPC1 induces ER stress, initiating immune activation in macrophages.

doi: 10.1242/jcs.237610

Figure Lengend Snippet: Fig. 5. Tunicamycin, brefeldin A and SKF96365 treatment induce autophagy and apoptosis in Raw 264.7 macrophages. (A) Representative immunoblot images showing expression of markers for the induction of autophagy and apoptosis in Raw 264.7 macrophages treated with 10 µM Tuni, BFA or SKF for 12 h. (B) Quantification of densitometric values (mean±s.d.) from bands as shown in A. (C) Representative microscopy images of Raw 264.7 macrophages stained for LC3B (green), CHOP (red) and DAPI (blue) after cells were exposed to 10 µM Tuni, BFA or SKF for 12 h. **P<0.01; ***P<0.001 by one-way ANOVA test. The data shown are representative of three independent experiments. Scale bars: 20 µm.

Article Snippet: Thereafter, the slides were washed again, and coverslip mounted using VECTASHIELD HardSet Mounting Media with DAPI (Vector Laboratories, Inc.).

Techniques: Western Blot, Expressing, Microscopy, Staining