vectamount h 5000 Search Results


mounting medium  (Vector Laboratories)
96
Vector Laboratories mounting medium
Mounting Medium, 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
https://www.bioz.com/result/mounting medium/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
mounting medium - by Bioz Stars, 2026-05
96/100 stars
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vectamount medium  (Vector Laboratories)
96
Vector Laboratories vectamount medium
Vectamount Medium, 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
https://www.bioz.com/result/vectamount medium/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
vectamount medium - by Bioz Stars, 2026-05
96/100 stars
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fluorescence with dapi  (Vector Laboratories)
96
Vector Laboratories fluorescence with dapi
WT and cd31 −/− EC monolayers were stimulated by MHC antibody-ligation or treated with an Isotype-matched control and secondary antibodies (2 h). Some cd31 −/− ECs were also treated with an Akt activator (500 nM, 3 h) prior to antibody stimulation. Vehicle was added in the untreated cultures (IsC and MHC ligation). a β-catenin and cMyc expression were determined by immunofluorescent antibody staining and wide-field microscopy. The nucleus was stained with <t>DAPI.</t> The <t>mean</t> <t>fluorescence</t> intensity of cMyc and β-catenin measured in 500 cells in three independent experiments is shown in ( b , c ), respectively. Scale bar = 40 μm. Data are mean ± SD. one-way Anova with Tuckey post-hoc test. b WT IsC vs WT MHC; c WT IsC vs WT MHC *** p = 0.0008, cd31 − / − IsC + C991 vs cd31 − / − MHC + C991 *** p = 0.0002. d , e : cMyc ( d ) and aldolase ( e ) gene transcription by WT (upper panels) and cd31 −/− (lower panels) EC at the indicated time points. n = 3 biologically independent samples, N = 2 independent experiments. Error bars represent SD. One-way Anova with Tuckey post-hoc test or T -test ( d , e ). d WT IsC 30′ vs WT MHC 30′ ** p = 0.003, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001; e WT IsC 30′ vs WT MHC 30′ *** p = 0.0008, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001, WT IsC 240′ vs WT MHC 240′ **** p < 0.0001.
Fluorescence 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
https://www.bioz.com/result/fluorescence with dapi/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
fluorescence with dapi - by Bioz Stars, 2026-05
96/100 stars
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vectamount permanent mounting medium vec-h-5000  (Biozol Diagnostica Vertrieb GmbH)
90
Biozol Diagnostica Vertrieb GmbH vectamount permanent mounting medium vec-h-5000
WT and cd31 −/− EC monolayers were stimulated by MHC antibody-ligation or treated with an Isotype-matched control and secondary antibodies (2 h). Some cd31 −/− ECs were also treated with an Akt activator (500 nM, 3 h) prior to antibody stimulation. Vehicle was added in the untreated cultures (IsC and MHC ligation). a β-catenin and cMyc expression were determined by immunofluorescent antibody staining and wide-field microscopy. The nucleus was stained with <t>DAPI.</t> The <t>mean</t> <t>fluorescence</t> intensity of cMyc and β-catenin measured in 500 cells in three independent experiments is shown in ( b , c ), respectively. Scale bar = 40 μm. Data are mean ± SD. one-way Anova with Tuckey post-hoc test. b WT IsC vs WT MHC; c WT IsC vs WT MHC *** p = 0.0008, cd31 − / − IsC + C991 vs cd31 − / − MHC + C991 *** p = 0.0002. d , e : cMyc ( d ) and aldolase ( e ) gene transcription by WT (upper panels) and cd31 −/− (lower panels) EC at the indicated time points. n = 3 biologically independent samples, N = 2 independent experiments. Error bars represent SD. One-way Anova with Tuckey post-hoc test or T -test ( d , e ). d WT IsC 30′ vs WT MHC 30′ ** p = 0.003, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001; e WT IsC 30′ vs WT MHC 30′ *** p = 0.0008, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001, WT IsC 240′ vs WT MHC 240′ **** p < 0.0001.
Vectamount Permanent Mounting Medium Vec H 5000, supplied by Biozol Diagnostica Vertrieb 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/vectamount permanent mounting medium vec-h-5000/product/Biozol Diagnostica Vertrieb GmbH
Average 90 stars, based on 1 article reviews
vectamount permanent mounting medium vec-h-5000 - by Bioz Stars, 2026-05
90/100 stars
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dab substrate kit for peroxidase  (Vector Laboratories)
96
Vector Laboratories dab substrate kit for peroxidase
WT and cd31 −/− EC monolayers were stimulated by MHC antibody-ligation or treated with an Isotype-matched control and secondary antibodies (2 h). Some cd31 −/− ECs were also treated with an Akt activator (500 nM, 3 h) prior to antibody stimulation. Vehicle was added in the untreated cultures (IsC and MHC ligation). a β-catenin and cMyc expression were determined by immunofluorescent antibody staining and wide-field microscopy. The nucleus was stained with <t>DAPI.</t> The <t>mean</t> <t>fluorescence</t> intensity of cMyc and β-catenin measured in 500 cells in three independent experiments is shown in ( b , c ), respectively. Scale bar = 40 μm. Data are mean ± SD. one-way Anova with Tuckey post-hoc test. b WT IsC vs WT MHC; c WT IsC vs WT MHC *** p = 0.0008, cd31 − / − IsC + C991 vs cd31 − / − MHC + C991 *** p = 0.0002. d , e : cMyc ( d ) and aldolase ( e ) gene transcription by WT (upper panels) and cd31 −/− (lower panels) EC at the indicated time points. n = 3 biologically independent samples, N = 2 independent experiments. Error bars represent SD. One-way Anova with Tuckey post-hoc test or T -test ( d , e ). d WT IsC 30′ vs WT MHC 30′ ** p = 0.003, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001; e WT IsC 30′ vs WT MHC 30′ *** p = 0.0008, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001, WT IsC 240′ vs WT MHC 240′ **** p < 0.0001.
Dab Substrate Kit For Peroxidase, 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
https://www.bioz.com/result/dab substrate kit for peroxidase/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
dab substrate kit for peroxidase - by Bioz Stars, 2026-05
96/100 stars
  Buy from Supplier
vectamount  (Vector Laboratories)
96
Vector Laboratories vectamount
WT and cd31 −/− EC monolayers were stimulated by MHC antibody-ligation or treated with an Isotype-matched control and secondary antibodies (2 h). Some cd31 −/− ECs were also treated with an Akt activator (500 nM, 3 h) prior to antibody stimulation. Vehicle was added in the untreated cultures (IsC and MHC ligation). a β-catenin and cMyc expression were determined by immunofluorescent antibody staining and wide-field microscopy. The nucleus was stained with <t>DAPI.</t> The <t>mean</t> <t>fluorescence</t> intensity of cMyc and β-catenin measured in 500 cells in three independent experiments is shown in ( b , c ), respectively. Scale bar = 40 μm. Data are mean ± SD. one-way Anova with Tuckey post-hoc test. b WT IsC vs WT MHC; c WT IsC vs WT MHC *** p = 0.0008, cd31 − / − IsC + C991 vs cd31 − / − MHC + C991 *** p = 0.0002. d , e : cMyc ( d ) and aldolase ( e ) gene transcription by WT (upper panels) and cd31 −/− (lower panels) EC at the indicated time points. n = 3 biologically independent samples, N = 2 independent experiments. Error bars represent SD. One-way Anova with Tuckey post-hoc test or T -test ( d , e ). d WT IsC 30′ vs WT MHC 30′ ** p = 0.003, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001; e WT IsC 30′ vs WT MHC 30′ *** p = 0.0008, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001, WT IsC 240′ vs WT MHC 240′ **** p < 0.0001.
Vectamount, 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
https://www.bioz.com/result/vectamount/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
vectamount - by Bioz Stars, 2026-05
96/100 stars
  Buy from Supplier

Image Search Results


WT and cd31 −/− EC monolayers were stimulated by MHC antibody-ligation or treated with an Isotype-matched control and secondary antibodies (2 h). Some cd31 −/− ECs were also treated with an Akt activator (500 nM, 3 h) prior to antibody stimulation. Vehicle was added in the untreated cultures (IsC and MHC ligation). a β-catenin and cMyc expression were determined by immunofluorescent antibody staining and wide-field microscopy. The nucleus was stained with DAPI. The mean fluorescence intensity of cMyc and β-catenin measured in 500 cells in three independent experiments is shown in ( b , c ), respectively. Scale bar = 40 μm. Data are mean ± SD. one-way Anova with Tuckey post-hoc test. b WT IsC vs WT MHC; c WT IsC vs WT MHC *** p = 0.0008, cd31 − / − IsC + C991 vs cd31 − / − MHC + C991 *** p = 0.0002. d , e : cMyc ( d ) and aldolase ( e ) gene transcription by WT (upper panels) and cd31 −/− (lower panels) EC at the indicated time points. n = 3 biologically independent samples, N = 2 independent experiments. Error bars represent SD. One-way Anova with Tuckey post-hoc test or T -test ( d , e ). d WT IsC 30′ vs WT MHC 30′ ** p = 0.003, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001; e WT IsC 30′ vs WT MHC 30′ *** p = 0.0008, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001, WT IsC 240′ vs WT MHC 240′ **** p < 0.0001.

Journal: Nature Communications

Article Title: Preservation of microvascular barrier function requires CD31 receptor-induced metabolic reprogramming

doi: 10.1038/s41467-020-17329-8

Figure Lengend Snippet: WT and cd31 −/− EC monolayers were stimulated by MHC antibody-ligation or treated with an Isotype-matched control and secondary antibodies (2 h). Some cd31 −/− ECs were also treated with an Akt activator (500 nM, 3 h) prior to antibody stimulation. Vehicle was added in the untreated cultures (IsC and MHC ligation). a β-catenin and cMyc expression were determined by immunofluorescent antibody staining and wide-field microscopy. The nucleus was stained with DAPI. The mean fluorescence intensity of cMyc and β-catenin measured in 500 cells in three independent experiments is shown in ( b , c ), respectively. Scale bar = 40 μm. Data are mean ± SD. one-way Anova with Tuckey post-hoc test. b WT IsC vs WT MHC; c WT IsC vs WT MHC *** p = 0.0008, cd31 − / − IsC + C991 vs cd31 − / − MHC + C991 *** p = 0.0002. d , e : cMyc ( d ) and aldolase ( e ) gene transcription by WT (upper panels) and cd31 −/− (lower panels) EC at the indicated time points. n = 3 biologically independent samples, N = 2 independent experiments. Error bars represent SD. One-way Anova with Tuckey post-hoc test or T -test ( d , e ). d WT IsC 30′ vs WT MHC 30′ ** p = 0.003, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001; e WT IsC 30′ vs WT MHC 30′ *** p = 0.0008, WT IsC 120′ vs WT MHC 120′ **** p < 0.0001, WT IsC 240′ vs WT MHC 240′ **** p < 0.0001.

Article Snippet: Coverslips were extensively washed, air dried, and mounted in Vectorshield (Vector Laboratories, H-5000) mounting medium for fluorescence with DAPI (Vector Laboratories, H-1800) or Hoechst (Sigma, 94403) on glass slides.

Techniques: Ligation, Expressing, Staining, Microscopy, Fluorescence