rat embryonic aortic smooth muscle cell line a7r5 bcrc60082 (BioResource International Inc)
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Rat Embryonic Aortic Smooth Muscle Cell Line A7r5 Bcrc60082, 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
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Average 90 stars, based on 1 article reviews
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1) Product Images from "Estrogen modulates vascular smooth muscle cell function through downregulation of SIRT1"
Article Title: Estrogen modulates vascular smooth muscle cell function through downregulation of SIRT1
Journal: Oncotarget
doi: 10.18632/oncotarget.22546
Figure Legend Snippet: ( A ), or over a time course with 10 nM E2 (0, 12, 24, and 48 h) ( B ); we subjected the samples to western blot analysis to quantify SIRT1, GAPDH, and α-tubulin protein expression. ( C ) We analyzed the NAD + /NADH ratio in A7r5 cells subjected to the indicated treatments. Data are expressed as mean ± standard deviation (SD). Representative data shown are from experiments performed independently at least 3 times. * p < 0.05
Techniques Used: Western Blot, Expressing, Standard Deviation
Figure Legend Snippet: ( A ) Representative immunoblots of protein samples from A7r5 cells treated with 10 nM and 100 nM E2 that were stained with antibodies against caspase 3, Ki-67, cyclin D1, and GAPDH. ( B ) We quantified caspase 3, Ki-67, and cyclin D1 protein expression by computer-assisted densitometry analysis and presented their ratios to GAPDH, relative to the control group. ( C ) We performed flow cytometry on A7r5 cells treated with 10 nM and 100 nM E2, in order to assess the percentage in the G1 phase of the cell cycle.
Techniques Used: Western Blot, Staining, Expressing, Control, Flow Cytometry
Figure Legend Snippet: Wound healing assays were performed on A7r5 cells treated with 10 nM and 100 nM E2 for ( A ) 8 h and ( B ) 12 h. Black arrows indicate the wound edge. The residual gap between the migrating cells from the opposing wound edge is expressed as a percentage of the initial scraped area. Data are expressed as mean ± SD. Representative data shown are from experiments performed independently at least 3 times. * p < 0.05
Techniques Used:
Figure Legend Snippet: ( A ) We treated A7r5 cells with 10 nM E2 with and without resveratrol (Res, 15 μM); we then performed western blot analyses to quantify the levels of SIRT1 and GAPDH. ( B ) We analyzed the NAD + /NADH ratio in the presence and absence of resveratrol. Data are expressed as mean ± SD. Representative data shown are from experiments performed independently at least 3 times. * p < 0.05
Techniques Used: Western Blot
Figure Legend Snippet: ( A ) Representative immunoblots of protein samples from A7r5 cells exposed to 10 nM E2 with and without resveratrol (Res, 15 μM), labeled with antibodies against caspase 3, Ki-67, cyclin D1, and GAPDH. ( B ) We quantified caspase 3, Ki-67, and cyclin D1 protein expression by computer-assisted densitometry analysis and presented their ratios to GAPDH, relative to the control group. ( C ) Flow cytometric analysis of A7r5 cells in the G1 phase of the cell cycle after treatment with 10 nM E2 with and without resveratrol (Res, 15 μM).
Techniques Used: Western Blot, Labeling, Expressing, Control
Figure Legend Snippet: Wound healing assays were performed on A7r5 cells treated with 10 nM E2, with and without resveratrol (Res, 15 μM) after ( A ) 8 h and ( B ) 12 h. One representative experiment is shown. Black arrows indicate the wound edge. The residual gap between the migrating cells from the opposing wound edge is expressed as a percentage of the initial scraped area. Data are expressed as mean ± SD. Representative data shown are from experiments performed independently at least 3 times. * p < 0.05
Techniques Used:
Figure Legend Snippet: Representative immunoblots of A7r5 cells treated with 10 nM E2, with and without resveratrol (Res, 15 μM), labeled with antibodies against SIRT1, p-Akt, Akt, p-ERK, ERK, and GAPDH.
Techniques Used: Western Blot, Labeling
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