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aoc3 protein content  (Novus Biologicals)
93
Novus Biologicals aoc3 protein content
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Aoc3 Protein Content, 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
https://www.bioz.com/product/vap-1/Mouse+VAP-1%2FAOC3+ELISA+Kit+(Colorimetric)/bio_rxiv__2025__10__14__682314-43-0-12
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aoc3 protein content - by Bioz Stars, 2026-09
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alexa fluor tm 647 conjugated mouse anti aoc3  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology alexa fluor tm 647 conjugated mouse anti aoc3
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Alexa Fluor Tm 647 Conjugated Mouse Anti Aoc3, supplied by Santa Cruz Biotechnology, 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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vap 1  (Astellas)
86
Astellas vap 1
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Vap 1, supplied by Astellas, 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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anti vap b antibody  (Proteintech)
95
Proteintech anti vap b antibody
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Anti Vap B Antibody, supplied by Proteintech, 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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vap b proteintech  (Proteintech)
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Proteintech vap b proteintech
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Vap B Proteintech, supplied by Proteintech, 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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vap b  (Proteintech)
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Proteintech vap b
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Vap B, supplied by Proteintech, 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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ab78547 vap b proteintech  (Proteintech)
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Proteintech ab78547 vap b proteintech
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Ab78547 Vap B Proteintech, supplied by Proteintech, 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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mvap 1  (R&D Systems)
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R&D Systems mvap 1
(a) Representative scheme illustrating the LV constructs utilized for overexpression of <t>AOC3</t> proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).
Mvap 1, supplied by R&D Systems, 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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(a) Representative scheme illustrating the LV constructs utilized for overexpression of AOC3 proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).

Journal: bioRxiv

Article Title: EctoShed : A novel Gene Delivery Platform for Functional Analysis of Adipocyte-Shed Proteoforms

doi: 10.1101/2025.10.14.682314

Figure Lengend Snippet: (a) Representative scheme illustrating the LV constructs utilized for overexpression of AOC3 proteoforms upon transduction of SVF-isolated primary white adipocytes (1° iWad) on day 4 of differentiation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a CMV promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3 , (d) m- sAoc3 in 1° iWad lysates. Fluorometric determination of AOC3 enzyme activity in (e) 1° iWad lysates and (f) 1° iWad supernatant. (g) Representative bright-field images of 1° iWad transduced with LV vectors (left); representative immunofluorescent (IF) images of 1° iWad transduced with LV vectors followed by DAPI and AOC3 labelling and (h) quantification of AOC3 in 1° iWad. Quantification of IF shows individual points for independent experiments. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,h).

Article Snippet: AOC3 protein content in serum and iWAT lysates was quantified by ELISA (Novus Biologicals, NBP2-78769) according to the manufacturer’s protocol and normalized to total protein or sample volume.

Techniques: Construct, Over Expression, Transduction, Isolation, Generated, Sequencing, Control, Expressing, Activity Assay, Two Tailed Test

Representative scheme illustrating the AAV constructs utilized for overexpression of AOC3 proteoforms in iWAT upon cirurgical preparation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a miniUcp1 promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3, and (d) m- sAoc3 in iWAT. (e) Expression levels of indicated genes in iWAT, eWAT, liver and brown adipose tissue (BAT). (f) Fluorometric determination of AOC3 enzyme activity in iWAT and AOC3 protein quantification by enzyme-linked sorbent assay (ELISA) in (g) iWAT lysates and (h) serum. (i) Representative western blot showing GFP and AOC3 protein content in iWAT of transduced mice. HSC70 was used as loading control. Relative expression quantification is annotated in the figure. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,g,h).

Journal: bioRxiv

Article Title: EctoShed : A novel Gene Delivery Platform for Functional Analysis of Adipocyte-Shed Proteoforms

doi: 10.1101/2025.10.14.682314

Figure Lengend Snippet: Representative scheme illustrating the AAV constructs utilized for overexpression of AOC3 proteoforms in iWAT upon cirurgical preparation: full length Aoc3 ; soluble Aoc3 mimic (m- sAoc3) generated by fusing Adiponectin signal peptide to the proximal extracellular sequence of Aoc3 ; and control construct expressing Gfp , under a miniUcp1 promoter. Generated using Biorender. Relative mRNA expression levels of (b) Gfp , (c) Aoc3, and (d) m- sAoc3 in iWAT. (e) Expression levels of indicated genes in iWAT, eWAT, liver and brown adipose tissue (BAT). (f) Fluorometric determination of AOC3 enzyme activity in iWAT and AOC3 protein quantification by enzyme-linked sorbent assay (ELISA) in (g) iWAT lysates and (h) serum. (i) Representative western blot showing GFP and AOC3 protein content in iWAT of transduced mice. HSC70 was used as loading control. Relative expression quantification is annotated in the figure. Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Unpaired, two-tailed Student’s test were performed (b,c,d), Non-parametric, Kruskal-Wallis with Dunn’s post hoc correction were performed (e,f,g,h).

Article Snippet: AOC3 protein content in serum and iWAT lysates was quantified by ELISA (Novus Biologicals, NBP2-78769) according to the manufacturer’s protocol and normalized to total protein or sample volume.

Techniques: Construct, Over Expression, Generated, Sequencing, Control, Expressing, Activity Assay, Enzyme-linked Immunosorbent Assay, Western Blot, Two Tailed Test

(a) Body weight (grams), (b) iWAT and (c) eWAT weight percentage relative to BW, and (d) fasted (6h) blood glucose levels 6 weeks after AAV-driven expression of m-s Aoc3 versus Gfp . Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Non-parametric, two-tailed Mann-Whitney t-test was performed (a,b,c,d).

Journal: bioRxiv

Article Title: EctoShed : A novel Gene Delivery Platform for Functional Analysis of Adipocyte-Shed Proteoforms

doi: 10.1101/2025.10.14.682314

Figure Lengend Snippet: (a) Body weight (grams), (b) iWAT and (c) eWAT weight percentage relative to BW, and (d) fasted (6h) blood glucose levels 6 weeks after AAV-driven expression of m-s Aoc3 versus Gfp . Statistics: bar graphs represent the mean + s.e.m. with all data point represented. Non-parametric, two-tailed Mann-Whitney t-test was performed (a,b,c,d).

Article Snippet: AOC3 protein content in serum and iWAT lysates was quantified by ELISA (Novus Biologicals, NBP2-78769) according to the manufacturer’s protocol and normalized to total protein or sample volume.

Techniques: Expressing, Two Tailed Test, MANN-WHITNEY