murine vsmc cell line movas Search Results


murine aortic vsmcs  (ATCC)
96
ATCC murine aortic vsmcs
GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. <t>(A)</t> <t>MOVAS</t> cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.
Murine Aortic Vsmcs, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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h end cells  (ATCC)
96
ATCC h end cells
GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. <t>(A)</t> <t>MOVAS</t> cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.
H End Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
h end cells - by Bioz Stars, 2026-04
96/100 stars
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primary murine aortic smooth muscle cells  (Jackson Laboratory)
90
Jackson Laboratory primary murine aortic smooth muscle cells
GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. <t>(A)</t> <t>MOVAS</t> cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.
Primary Murine Aortic Smooth Muscle Cells, supplied by Jackson Laboratory, 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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Average 90 stars, based on 1 article reviews
primary murine aortic smooth muscle cells - by Bioz Stars, 2026-04
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murine vascular smooth muscle sv40lt smc cells vsmcs  (ATCC)
97
ATCC murine vascular smooth muscle sv40lt smc cells vsmcs
GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. <t>(A)</t> <t>MOVAS</t> cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.
Murine Vascular Smooth Muscle Sv40lt Smc Cells Vsmcs, supplied by ATCC, 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/murine vascular smooth muscle sv40lt smc cells vsmcs/product/ATCC
Average 97 stars, based on 1 article reviews
murine vascular smooth muscle sv40lt smc cells vsmcs - by Bioz Stars, 2026-04
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primary murine vascular smooth muscle cells  (ScienCell)
90
ScienCell primary murine vascular smooth muscle cells
GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. <t>(A)</t> <t>MOVAS</t> cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.
Primary Murine Vascular Smooth Muscle Cells, 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 murine vascular smooth muscle cells/product/ScienCell
Average 90 stars, based on 1 article reviews
primary murine vascular smooth muscle cells - by Bioz Stars, 2026-04
90/100 stars
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murine vsmc  (Charles River Laboratories)
90
Charles River Laboratories murine vsmc
GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. <t>(A)</t> <t>MOVAS</t> cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.
Murine Vsmc, supplied by Charles River Laboratories, 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/murine vsmc/product/Charles River Laboratories
Average 90 stars, based on 1 article reviews
murine vsmc - by Bioz Stars, 2026-04
90/100 stars
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Image Search Results


GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. (A) MOVAS cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.

Journal: Frontiers in Cell and Developmental Biology

Article Title: GFOGER Peptide Modifies the Protein Content of Extracellular Vesicles and Inhibits Vascular Calcification

doi: 10.3389/fcell.2020.589761

Figure Lengend Snippet: GFOGER peptide inhibits Pi-induced calcification: (A,B) in smooth muscle cells. Calcification in smooth muscle cells was induced by incubation with 4 mM Pi in absence or presence of GFOGER peptide or GOERFG peptide. (A) MOVAS cells were incubated with two concentrations of GFOGER peptide (250 and 500 μM) or with 500 μM of GOERFG peptide for 10 days. (B) Primary human vascular smooth muscle cells were incubated with 500 μM of GFOGER peptide for 14 days. Calcification was then measured using the OCP method. (C,D) In rat aortic rings. Rat aortic rings were incubated with 4 mM Pi in presence or absence of 500 μM GFOGER peptide for 10 days. (C) Images of one representative Alizarin Red staining experiment are shown. (D) Intracellular calcium content was quantified by OCP colorimetric method. Data are expressed as mean ± SEM of three independent experiments done in triplicate ( n = 3). *** p < 0.001 vs. 4 mM Pi. Parametric one-way ANOVA test.

Article Snippet: Murine aortic VSMCs (MOVAS-1 CRL-2797, ATCC, Manassas, VA, United States) were maintained in DMEM 6546 medium supplemented with 10% FCS, 100 IU/ml penicillin, 100 μg/ml streptomycin, 4 mM glutamine, and 200 μg/ml geneticin (G418) at 37°C in a humidified 5% CO 2 atmosphere.

Techniques: Incubation, Staining