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myh6 atrium specific myosin heavy chain mouse igg  (Developmental Studies Hybridoma Bank)
99
Developmental Studies Hybridoma Bank myh6 atrium specific myosin heavy chain mouse igg
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Myh6 Atrium Specific Myosin Heavy Chain Mouse Igg, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/myh6 atrium specific myosin heavy chain mouse igg/product/Developmental Studies Hybridoma Bank
Average 99 stars, based on 1 article reviews
myh6 atrium specific myosin heavy chain mouse igg - by Bioz Stars, 2026-03
99/100 stars
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nasal atriums  (Copan Diagnostics)
97
Copan Diagnostics nasal atriums
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Nasal Atriums, supplied by Copan Diagnostics, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/nasal atriums/product/Copan Diagnostics
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nasal atriums - by Bioz Stars, 2026-03
97/100 stars
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atrium 3 0 version  (Danaher Inc)
86
Danaher Inc atrium 3 0 version
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Atrium 3 0 Version, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/atrium 3 0 version/product/Danaher Inc
Average 86 stars, based on 1 article reviews
atrium 3 0 version - by Bioz Stars, 2026-03
86/100 stars
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stainless steel and polytetrafluoroethylene encapsulated stent atrium advanta v12 over-the-wire (otw) covered stents  (Atrium Medical Corporation)
90
Atrium Medical Corporation stainless steel and polytetrafluoroethylene encapsulated stent atrium advanta v12 over-the-wire (otw) covered stents
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Stainless Steel And Polytetrafluoroethylene Encapsulated Stent Atrium Advanta V12 Over The Wire (Otw) Covered Stents, supplied by Atrium Medical Corporation, 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/stainless steel and polytetrafluoroethylene encapsulated stent atrium advanta v12 over-the-wire (otw) covered stents/product/Atrium Medical Corporation
Average 90 stars, based on 1 article reviews
stainless steel and polytetrafluoroethylene encapsulated stent atrium advanta v12 over-the-wire (otw) covered stents - by Bioz Stars, 2026-03
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sma atrium brand air sampling device  (Veltek Inc)
90
Veltek Inc sma atrium brand air sampling device
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Sma Atrium Brand Air Sampling Device, supplied by Veltek 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/sma atrium brand air sampling device/product/Veltek Inc
Average 90 stars, based on 1 article reviews
sma atrium brand air sampling device - by Bioz Stars, 2026-03
90/100 stars
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atrium advanta v12 cbe stents  (Getinge AB)
90
Getinge AB atrium advanta v12 cbe stents
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Atrium Advanta V12 Cbe Stents, supplied by Getinge AB, 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/atrium advanta v12 cbe stents/product/Getinge AB
Average 90 stars, based on 1 article reviews
atrium advanta v12 cbe stents - by Bioz Stars, 2026-03
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ptfe atrium advanta vascular graft  (Getinge AB)
90
Getinge AB ptfe atrium advanta vascular graft
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Ptfe Atrium Advanta Vascular Graft, supplied by Getinge AB, 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/ptfe atrium advanta vascular graft/product/Getinge AB
Average 90 stars, based on 1 article reviews
ptfe atrium advanta vascular graft - by Bioz Stars, 2026-03
90/100 stars
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left-atrium volume index (lavi)  (PolaRx Biopharmaceuticals Inc)
90
PolaRx Biopharmaceuticals Inc left-atrium volume index (lavi)
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Left Atrium Volume Index (Lavi), supplied by PolaRx Biopharmaceuticals 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/left-atrium volume index (lavi)/product/PolaRx Biopharmaceuticals Inc
Average 90 stars, based on 1 article reviews
left-atrium volume index (lavi) - by Bioz Stars, 2026-03
90/100 stars
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atrium version 9.1.0  (Banook Group)
90
Banook Group atrium version 9.1.0
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
Atrium Version 9.1.0, supplied by Banook Group, 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/atrium version 9.1.0/product/Banook Group
Average 90 stars, based on 1 article reviews
atrium version 9.1.0 - by Bioz Stars, 2026-03
90/100 stars
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right atrium boston scientific electrode  (Boston Scientific Corporation)
90
Boston Scientific Corporation right atrium boston scientific electrode
α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- <t>MYH6</t> (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.
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α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- MYH6 (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.

Journal: iScience

Article Title: α- and β-myosin II can be non-uniformly distributed within the cardiac sarcomere

doi: 10.1016/j.isci.2025.112233

Figure Lengend Snippet: α- and β-myosin II can exhibit unique distributions within cardiac sarcomeres (A) Representative example of IF of endogenous β-myosin II (top) and expression of mEGFP- MYH6 (middle) in a hiCM; bottom shows overlay. Scale bars: left 10 μm, right 2 μm. (B) Line scan from yellow boxes in (A). (C) Average of all line scans (20 cells, 772 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. (D) Top: expression of mNeon- MYH7 and IF of endogenous α-myosin II in a representative hiCM. Bottom: Average of all line scans (15 cells, 456 sarcomeres, 3 independent experiments). Lines show population-averaged mean value while shaded bands show ± standard error of the mean. White brackets denote individual filament stacks. Scale bar: 2 μm. (E) Distance each myosin II extended from filament center in hiCMs (β-myosin II IF: 14 cells, 280 measurements; α-myosin II IF: 15 cells, 300 measurements; mNeon- MYH7 (β expressed): 15 cells, 300 measurements; mEGFP- MYH6 (α expressed): 15 cells, 300 measurements). p -values in grey (Welch's t-test). (F) Simplified model of the potential arrangement of β-myosin II (magenta) and α-myosin II (green) in thick filaments of iPSC-derived cardiac myocyte sarcomeres. (G) Left: IF using antibodies against β-myosin II (top) and α-myosin II (bottom) in different sections of human ventricle; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 280 measurements; α-myosin II: 321 measurements). Scale bar: 2 μm. p -values in grey (Welch's t-test). (H) Left: individual β-myosin II (ventricle) and α-myosin II (atrium) whole-mount immunofluorescence stains in 72 h post-fertilization zebrafish embryos; right: distance the fluorescent signal of each myosin extended from the filament center (β-myosin II: 14 embryos, 222 measurements; α-myosin II: 13 embryos, 102 measurements). White brackets in each image denote individual filament stacks. Scale bar: 2 μm. p -values in grey (Welch's t-test); (I) AlphaFold3-predicted model of α-myosin II/β-myosin II heavy chain ( MYH6 / MYH7 genes, respectively) motors + motor/lever arms, modeled with MYL2 / MYL3 (gray), which encode the ventricular essential/regulatory myosin light chains (a similar AlphaFold3-predicted model, but modeled with atrial essential/regulatory myosin light chains instead of ventricular light chains, is shown in ). N1, 2, and 3 in (E), (G), and (H) represent individual biological replicates, color-coded by replicate.

Article Snippet: MYH6: atrium-specific myosin heavy chain mouse IgG , Developmental Studies Hybridoma Bank (DSHB) , Cat# S46; RRID: AB_528376.

Techniques: Expressing, Derivative Assay, Immunofluorescence

Journal: iScience

Article Title: α- and β-myosin II can be non-uniformly distributed within the cardiac sarcomere

doi: 10.1016/j.isci.2025.112233

Figure Lengend Snippet:

Article Snippet: MYH6: atrium-specific myosin heavy chain mouse IgG , Developmental Studies Hybridoma Bank (DSHB) , Cat# S46; RRID: AB_528376.

Techniques: Recombinant, Plasmid Preparation, Software