primary human vsmc Search Results


90
Cambrex primary human vsmc from coronary arteries
Primary Human Vsmc From Coronary Arteries, supplied by Cambrex, 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/primary human vsmc from coronary arteries/product/Cambrex
Average 90 stars, based on 1 article reviews
primary human vsmc from coronary arteries - by Bioz Stars, 2026-03
90/100 stars
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90
ScienCell primary human vsmc
Flow cytometry gates for cell viability were set based on living and EtOH-killed controls (A). Incubation for 2 h (grey bar) with pDNA had no impact on vascular smooth muscle cell <t>(vSMC)</t> viability. Fifty-percent pCsM (C) and Cs (D) stabilize vSMC viability by 12 h post-incubation, whereas Vehicle (E) exposure drives protracted declines. Cell viability was unchanged 24 h after 20% treatments (F). (*p≤0.01, §p≤0.05)
Primary Human Vsmc, supplied by ScienCell, 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/primary human vsmc/product/ScienCell
Average 90 stars, based on 1 article reviews
primary human vsmc - by Bioz Stars, 2026-03
90/100 stars
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90
ScienCell primary human cerebral vsmc
Flow cytometry gates for cell viability were set based on living and EtOH-killed controls (A). Incubation for 2 h (grey bar) with pDNA had no impact on vascular smooth muscle cell <t>(vSMC)</t> viability. Fifty-percent pCsM (C) and Cs (D) stabilize vSMC viability by 12 h post-incubation, whereas Vehicle (E) exposure drives protracted declines. Cell viability was unchanged 24 h after 20% treatments (F). (*p≤0.01, §p≤0.05)
Primary Human Cerebral Vsmc, supplied by ScienCell, 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/primary human cerebral vsmc/product/ScienCell
Average 90 stars, based on 1 article reviews
primary human cerebral vsmc - by Bioz Stars, 2026-03
90/100 stars
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90
BioResource International Inc human primary vascular smooth muscle cells (vsmc)
Flow cytometry gates for cell viability were set based on living and EtOH-killed controls (A). Incubation for 2 h (grey bar) with pDNA had no impact on vascular smooth muscle cell <t>(vSMC)</t> viability. Fifty-percent pCsM (C) and Cs (D) stabilize vSMC viability by 12 h post-incubation, whereas Vehicle (E) exposure drives protracted declines. Cell viability was unchanged 24 h after 20% treatments (F). (*p≤0.01, §p≤0.05)
Human Primary Vascular Smooth Muscle Cells (Vsmc), supplied by BioResource International 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/human primary vascular smooth muscle cells (vsmc)/product/BioResource International Inc
Average 90 stars, based on 1 article reviews
human primary vascular smooth muscle cells (vsmc) - by Bioz Stars, 2026-03
90/100 stars
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90
Lonza primary vsmc from human aorta rtery
Flow cytometry gates for cell viability were set based on living and EtOH-killed controls (A). Incubation for 2 h (grey bar) with pDNA had no impact on vascular smooth muscle cell <t>(vSMC)</t> viability. Fifty-percent pCsM (C) and Cs (D) stabilize vSMC viability by 12 h post-incubation, whereas Vehicle (E) exposure drives protracted declines. Cell viability was unchanged 24 h after 20% treatments (F). (*p≤0.01, §p≤0.05)
Primary Vsmc From Human Aorta Rtery, supplied by Lonza, 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/primary vsmc from human aorta rtery/product/Lonza
Average 90 stars, based on 1 article reviews
primary vsmc from human aorta rtery - by Bioz Stars, 2026-03
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Image Search Results


Flow cytometry gates for cell viability were set based on living and EtOH-killed controls (A). Incubation for 2 h (grey bar) with pDNA had no impact on vascular smooth muscle cell (vSMC) viability. Fifty-percent pCsM (C) and Cs (D) stabilize vSMC viability by 12 h post-incubation, whereas Vehicle (E) exposure drives protracted declines. Cell viability was unchanged 24 h after 20% treatments (F). (*p≤0.01, §p≤0.05)

Journal: Carbohydrate polymers

Article Title: Stability and Bioactivity of Chitosan as a Transfection Agent in Primary Human Cell Cultures: A Case for Chitosan-only Controls

doi: 10.1016/j.carbpol.2017.10.021

Figure Lengend Snippet: Flow cytometry gates for cell viability were set based on living and EtOH-killed controls (A). Incubation for 2 h (grey bar) with pDNA had no impact on vascular smooth muscle cell (vSMC) viability. Fifty-percent pCsM (C) and Cs (D) stabilize vSMC viability by 12 h post-incubation, whereas Vehicle (E) exposure drives protracted declines. Cell viability was unchanged 24 h after 20% treatments (F). (*p≤0.01, §p≤0.05)

Article Snippet: 2.2.1 Culture Primary human vSMC from ScienCell (Catalog #1100, Carlsbad, California) were cultured under standard conditions (5% CO 2 at 37 °C) in Medium 231 containing 5% Smooth Muscle Growth Supplement (Gibco), 0.1 mg/mL Primocin (Invivogen, San Diego, California), and 100 U/mL each penicillin and streptomycin (Life Technologies, Thermo Fisher Scientific) in BioCoat Collagen I culture flasks (Corning, New York).

Techniques: Flow Cytometry, Incubation

Flow cytometry gates to determine Live CD59-positive vSMC were set based on living and EtOH-killed controls (A). Chitosan (pCsM, CsM, Cs) initially decreased the number of CD59-positive cells (B, p≤0.001), an effect that was rapidly, potently and durably reversed, especially in the case of Cs (C, *p≤0.01, §p≤0.05).

Journal: Carbohydrate polymers

Article Title: Stability and Bioactivity of Chitosan as a Transfection Agent in Primary Human Cell Cultures: A Case for Chitosan-only Controls

doi: 10.1016/j.carbpol.2017.10.021

Figure Lengend Snippet: Flow cytometry gates to determine Live CD59-positive vSMC were set based on living and EtOH-killed controls (A). Chitosan (pCsM, CsM, Cs) initially decreased the number of CD59-positive cells (B, p≤0.001), an effect that was rapidly, potently and durably reversed, especially in the case of Cs (C, *p≤0.01, §p≤0.05).

Article Snippet: 2.2.1 Culture Primary human vSMC from ScienCell (Catalog #1100, Carlsbad, California) were cultured under standard conditions (5% CO 2 at 37 °C) in Medium 231 containing 5% Smooth Muscle Growth Supplement (Gibco), 0.1 mg/mL Primocin (Invivogen, San Diego, California), and 100 U/mL each penicillin and streptomycin (Life Technologies, Thermo Fisher Scientific) in BioCoat Collagen I culture flasks (Corning, New York).

Techniques: Flow Cytometry

Mean fluorescent intensity from flow cytometry was used to approximate average CD59 expression vSMC (A). CD59 is transiently depressed by pCsM, CsM and Cs (B, p≤0.001) but recovers to baseline by 24 h despite the presence of Vehicle (C). In the absence of chitosan, Vehicle decreases CD59 expression.

Journal: Carbohydrate polymers

Article Title: Stability and Bioactivity of Chitosan as a Transfection Agent in Primary Human Cell Cultures: A Case for Chitosan-only Controls

doi: 10.1016/j.carbpol.2017.10.021

Figure Lengend Snippet: Mean fluorescent intensity from flow cytometry was used to approximate average CD59 expression vSMC (A). CD59 is transiently depressed by pCsM, CsM and Cs (B, p≤0.001) but recovers to baseline by 24 h despite the presence of Vehicle (C). In the absence of chitosan, Vehicle decreases CD59 expression.

Article Snippet: 2.2.1 Culture Primary human vSMC from ScienCell (Catalog #1100, Carlsbad, California) were cultured under standard conditions (5% CO 2 at 37 °C) in Medium 231 containing 5% Smooth Muscle Growth Supplement (Gibco), 0.1 mg/mL Primocin (Invivogen, San Diego, California), and 100 U/mL each penicillin and streptomycin (Life Technologies, Thermo Fisher Scientific) in BioCoat Collagen I culture flasks (Corning, New York).

Techniques: Flow Cytometry, Expressing