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rabbit anti ip3r1 nbp2 22458 antibodies  (Novus Biologicals)
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Novus Biologicals rabbit anti ip3r1 nbp2 22458 antibodies
Rabbit Anti Ip3r1 Nbp2 22458 Antibodies, supplied by Novus Biologicals, 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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rabbit anti ip3r1  (Proteintech)
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rabbit anti-ip3r1 nbp2-22458  (Novus Biologicals)
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Rabbit Anti Ip3r1 Nbp2 22458, supplied by Novus Biologicals, 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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rabbit anti-ip3r1 antibodies  (Novus Biologicals)
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DENV and ZIKV infection decrease the interactions between ERMC proteins (A) Schematic representation of ERMC tethering complexes. Created with BioRender.com . (B and C) Huh7.5 cells were infected with DENV 16681s (MOI = 1) or ZIKV H/PF/2013 (MOI = 10) or left uninfected. Two or three days later, cells were fixed and subjected to proximity ligation assays (PLA) to detect (B) SYNJ2BP-RRBP1 or (C) VAPB-PTPIP51 interactions, and immunostained for NS3 viral protein to identify infected cells. Cells were imaged using confocal microscopy. Representative images are shown. Scale bar = 20 μm. (D) Quantification of PLA dot abundance for RRBP1-SYNJ2BP, VAPB-PTPIP51, and <t>IP3R1-VDAC1</t> interactions in uninfected- and infected cells from two independent experiments. Values in the 5%–95% percentile range are shown. ∗∗∗∗: p ≤ 0.0001; ∗: p ≤ 0.05; Kruskal-Wallis test for all except for RRBP1-SYNJ2BP 72hpi dataset (normal distribution of the data for the three conditions), which was analyzed with a one-way ANOVA test. Between 40 and 90 cells per condition over 2 independent experiments were analyzed. The “Ab alone” specificity controls were not taken into account for the statistical analysis.
Rabbit Anti Ip3r1 Antibodies, supplied by Novus Biologicals, 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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rabbit anti ip3r1 proteintech 19962 1 ap  (Proteintech)
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DENV and ZIKV infection decrease the interactions between ERMC proteins (A) Schematic representation of ERMC tethering complexes. Created with BioRender.com . (B and C) Huh7.5 cells were infected with DENV 16681s (MOI = 1) or ZIKV H/PF/2013 (MOI = 10) or left uninfected. Two or three days later, cells were fixed and subjected to proximity ligation assays (PLA) to detect (B) SYNJ2BP-RRBP1 or (C) VAPB-PTPIP51 interactions, and immunostained for NS3 viral protein to identify infected cells. Cells were imaged using confocal microscopy. Representative images are shown. Scale bar = 20 μm. (D) Quantification of PLA dot abundance for RRBP1-SYNJ2BP, VAPB-PTPIP51, and <t>IP3R1-VDAC1</t> interactions in uninfected- and infected cells from two independent experiments. Values in the 5%–95% percentile range are shown. ∗∗∗∗: p ≤ 0.0001; ∗: p ≤ 0.05; Kruskal-Wallis test for all except for RRBP1-SYNJ2BP 72hpi dataset (normal distribution of the data for the three conditions), which was analyzed with a one-way ANOVA test. Between 40 and 90 cells per condition over 2 independent experiments were analyzed. The “Ab alone” specificity controls were not taken into account for the statistical analysis.
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DENV and ZIKV infection decrease the interactions between ERMC proteins (A) Schematic representation of ERMC tethering complexes. Created with BioRender.com . (B and C) Huh7.5 cells were infected with DENV 16681s (MOI = 1) or ZIKV H/PF/2013 (MOI = 10) or left uninfected. Two or three days later, cells were fixed and subjected to proximity ligation assays (PLA) to detect (B) SYNJ2BP-RRBP1 or (C) VAPB-PTPIP51 interactions, and immunostained for NS3 viral protein to identify infected cells. Cells were imaged using confocal microscopy. Representative images are shown. Scale bar = 20 μm. (D) Quantification of PLA dot abundance for RRBP1-SYNJ2BP, VAPB-PTPIP51, and <t>IP3R1-VDAC1</t> interactions in uninfected- and infected cells from two independent experiments. Values in the 5%–95% percentile range are shown. ∗∗∗∗: p ≤ 0.0001; ∗: p ≤ 0.05; Kruskal-Wallis test for all except for RRBP1-SYNJ2BP 72hpi dataset (normal distribution of the data for the three conditions), which was analyzed with a one-way ANOVA test. Between 40 and 90 cells per condition over 2 independent experiments were analyzed. The “Ab alone” specificity controls were not taken into account for the statistical analysis.
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rabbit anti-ip3r1  (Thermo Fisher)
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DENV and ZIKV infection decrease the interactions between ERMC proteins (A) Schematic representation of ERMC tethering complexes. Created with BioRender.com . (B and C) Huh7.5 cells were infected with DENV 16681s (MOI = 1) or ZIKV H/PF/2013 (MOI = 10) or left uninfected. Two or three days later, cells were fixed and subjected to proximity ligation assays (PLA) to detect (B) SYNJ2BP-RRBP1 or (C) VAPB-PTPIP51 interactions, and immunostained for NS3 viral protein to identify infected cells. Cells were imaged using confocal microscopy. Representative images are shown. Scale bar = 20 μm. (D) Quantification of PLA dot abundance for RRBP1-SYNJ2BP, VAPB-PTPIP51, and <t>IP3R1-VDAC1</t> interactions in uninfected- and infected cells from two independent experiments. Values in the 5%–95% percentile range are shown. ∗∗∗∗: p ≤ 0.0001; ∗: p ≤ 0.05; Kruskal-Wallis test for all except for RRBP1-SYNJ2BP 72hpi dataset (normal distribution of the data for the three conditions), which was analyzed with a one-way ANOVA test. Between 40 and 90 cells per condition over 2 independent experiments were analyzed. The “Ab alone” specificity controls were not taken into account for the statistical analysis.
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rabbit anti-ip3r1 pa1-901  (Thermo Fisher)
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DENV and ZIKV infection decrease the interactions between ERMC proteins (A) Schematic representation of ERMC tethering complexes. Created with BioRender.com . (B and C) Huh7.5 cells were infected with DENV 16681s (MOI = 1) or ZIKV H/PF/2013 (MOI = 10) or left uninfected. Two or three days later, cells were fixed and subjected to proximity ligation assays (PLA) to detect (B) SYNJ2BP-RRBP1 or (C) VAPB-PTPIP51 interactions, and immunostained for NS3 viral protein to identify infected cells. Cells were imaged using confocal microscopy. Representative images are shown. Scale bar = 20 μm. (D) Quantification of PLA dot abundance for RRBP1-SYNJ2BP, VAPB-PTPIP51, and <t>IP3R1-VDAC1</t> interactions in uninfected- and infected cells from two independent experiments. Values in the 5%–95% percentile range are shown. ∗∗∗∗: p ≤ 0.0001; ∗: p ≤ 0.05; Kruskal-Wallis test for all except for RRBP1-SYNJ2BP 72hpi dataset (normal distribution of the data for the three conditions), which was analyzed with a one-way ANOVA test. Between 40 and 90 cells per condition over 2 independent experiments were analyzed. The “Ab alone” specificity controls were not taken into account for the statistical analysis.
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Image Search Results


Journal: iScience

Article Title: Dengue virus and Zika virus alter endoplasmic reticulum-mitochondria contact sites to regulate respiration and apoptosis

doi: 10.1016/j.isci.2024.111599

Figure Lengend Snippet:

Article Snippet: Rabbit anti-IP3R1 , Novus Biologicals , NBP2-22458.

Techniques: Produced, Virus, Recombinant, Software

DENV and ZIKV infection decrease the interactions between ERMC proteins (A) Schematic representation of ERMC tethering complexes. Created with BioRender.com . (B and C) Huh7.5 cells were infected with DENV 16681s (MOI = 1) or ZIKV H/PF/2013 (MOI = 10) or left uninfected. Two or three days later, cells were fixed and subjected to proximity ligation assays (PLA) to detect (B) SYNJ2BP-RRBP1 or (C) VAPB-PTPIP51 interactions, and immunostained for NS3 viral protein to identify infected cells. Cells were imaged using confocal microscopy. Representative images are shown. Scale bar = 20 μm. (D) Quantification of PLA dot abundance for RRBP1-SYNJ2BP, VAPB-PTPIP51, and IP3R1-VDAC1 interactions in uninfected- and infected cells from two independent experiments. Values in the 5%–95% percentile range are shown. ∗∗∗∗: p ≤ 0.0001; ∗: p ≤ 0.05; Kruskal-Wallis test for all except for RRBP1-SYNJ2BP 72hpi dataset (normal distribution of the data for the three conditions), which was analyzed with a one-way ANOVA test. Between 40 and 90 cells per condition over 2 independent experiments were analyzed. The “Ab alone” specificity controls were not taken into account for the statistical analysis.

Journal: iScience

Article Title: Dengue virus and Zika virus alter endoplasmic reticulum-mitochondria contact sites to regulate respiration and apoptosis

doi: 10.1016/j.isci.2024.111599

Figure Lengend Snippet: DENV and ZIKV infection decrease the interactions between ERMC proteins (A) Schematic representation of ERMC tethering complexes. Created with BioRender.com . (B and C) Huh7.5 cells were infected with DENV 16681s (MOI = 1) or ZIKV H/PF/2013 (MOI = 10) or left uninfected. Two or three days later, cells were fixed and subjected to proximity ligation assays (PLA) to detect (B) SYNJ2BP-RRBP1 or (C) VAPB-PTPIP51 interactions, and immunostained for NS3 viral protein to identify infected cells. Cells were imaged using confocal microscopy. Representative images are shown. Scale bar = 20 μm. (D) Quantification of PLA dot abundance for RRBP1-SYNJ2BP, VAPB-PTPIP51, and IP3R1-VDAC1 interactions in uninfected- and infected cells from two independent experiments. Values in the 5%–95% percentile range are shown. ∗∗∗∗: p ≤ 0.0001; ∗: p ≤ 0.05; Kruskal-Wallis test for all except for RRBP1-SYNJ2BP 72hpi dataset (normal distribution of the data for the three conditions), which was analyzed with a one-way ANOVA test. Between 40 and 90 cells per condition over 2 independent experiments were analyzed. The “Ab alone” specificity controls were not taken into account for the statistical analysis.

Article Snippet: Rabbit anti-IP3R1 (NBP2-22458) antibodies were obtained from Novus Biologicals.

Techniques: Infection, Ligation, Confocal Microscopy

Journal: iScience

Article Title: Dengue virus and Zika virus alter endoplasmic reticulum-mitochondria contact sites to regulate respiration and apoptosis

doi: 10.1016/j.isci.2024.111599

Figure Lengend Snippet:

Article Snippet: Rabbit anti-IP3R1 (NBP2-22458) antibodies were obtained from Novus Biologicals.

Techniques: Produced, Virus, Recombinant, Software