Review



msd 96-well multi-array rat vegf assay kit  (Meso Scale Diagnostics LLC)

 
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    Meso Scale Diagnostics LLC msd 96-well multi-array rat vegf assay kit
    TNF-α induced cell proliferation of RAECs. (A) Time-course and dose-response of RAEC proliferation following treatment with TNF-α. (B) Number of viable cells at 48 h following treatment with various concentrations of TNF-α. RAECs were seeded in a 96-well plate and were treated with various doses of TNF-α for 48 h; the number of viable cells was determined at the end of the experiment. Data are presented as the mean ± standard deviation of 6–10 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.
    Msd 96 Well Multi Array Rat Vegf Assay Kit, supplied by Meso Scale Diagnostics LLC, 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/product/msd+96-well+multi-array+rat+vegf+assay+kit/pmc05364956-77-14-25?v=Meso+Scale+Diagnostics+LLC
    Average 90 stars, based on 1 article reviews
    msd 96-well multi-array rat vegf assay kit - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "Slit2 suppresses endothelial cell proliferation and migration by inhibiting the VEGF-Notch signaling pathway"

    Article Title: Slit2 suppresses endothelial cell proliferation and migration by inhibiting the VEGF-Notch signaling pathway

    Journal: Molecular Medicine Reports

    doi: 10.3892/mmr.2017.6240

    TNF-α induced cell proliferation of RAECs. (A) Time-course and dose-response of RAEC proliferation following treatment with TNF-α. (B) Number of viable cells at 48 h following treatment with various concentrations of TNF-α. RAECs were seeded in a 96-well plate and were treated with various doses of TNF-α for 48 h; the number of viable cells was determined at the end of the experiment. Data are presented as the mean ± standard deviation of 6–10 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.
    Figure Legend Snippet: TNF-α induced cell proliferation of RAECs. (A) Time-course and dose-response of RAEC proliferation following treatment with TNF-α. (B) Number of viable cells at 48 h following treatment with various concentrations of TNF-α. RAECs were seeded in a 96-well plate and were treated with various doses of TNF-α for 48 h; the number of viable cells was determined at the end of the experiment. Data are presented as the mean ± standard deviation of 6–10 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.

    Techniques Used: Standard Deviation, Control

    TNF-α enhanced migratory ability of RAECs. (A) Migration was detected using a Transwell assay (magnification, ×100). (B) Compared with the control group, the migratory ability of RAECs was significantly increased in the TNF-α conditioned medium group. A concentration of 10 ng/ml TNF-α was used for the migration analysis. The control group was incubated in endothelial cell medium. Data are presented as the mean ± standard deviation of 6 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.
    Figure Legend Snippet: TNF-α enhanced migratory ability of RAECs. (A) Migration was detected using a Transwell assay (magnification, ×100). (B) Compared with the control group, the migratory ability of RAECs was significantly increased in the TNF-α conditioned medium group. A concentration of 10 ng/ml TNF-α was used for the migration analysis. The control group was incubated in endothelial cell medium. Data are presented as the mean ± standard deviation of 6 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.

    Techniques Used: Migration, Transwell Assay, Control, Concentration Assay, Incubation, Standard Deviation



    Similar Products

    msd 96-well multi-array rat vegf assay kit  (Meso Scale Diagnostics LLC)
    90
    Meso Scale Diagnostics LLC msd 96-well multi-array rat vegf assay kit
    TNF-α induced cell proliferation of RAECs. (A) Time-course and dose-response of RAEC proliferation following treatment with TNF-α. (B) Number of viable cells at 48 h following treatment with various concentrations of TNF-α. RAECs were seeded in a 96-well plate and were treated with various doses of TNF-α for 48 h; the number of viable cells was determined at the end of the experiment. Data are presented as the mean ± standard deviation of 6–10 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.
    Msd 96 Well Multi Array Rat Vegf Assay Kit, supplied by Meso Scale Diagnostics LLC, 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/product/msd+96-well+multi-array+rat+vegf+assay+kit/pmc05364956-77-14-25?v=Meso+Scale+Diagnostics+LLC
    Average 90 stars, based on 1 article reviews
    msd 96-well multi-array rat vegf assay kit - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    TNF-α induced cell proliferation of RAECs. (A) Time-course and dose-response of RAEC proliferation following treatment with TNF-α. (B) Number of viable cells at 48 h following treatment with various concentrations of TNF-α. RAECs were seeded in a 96-well plate and were treated with various doses of TNF-α for 48 h; the number of viable cells was determined at the end of the experiment. Data are presented as the mean ± standard deviation of 6–10 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.

    Journal: Molecular Medicine Reports

    Article Title: Slit2 suppresses endothelial cell proliferation and migration by inhibiting the VEGF-Notch signaling pathway

    doi: 10.3892/mmr.2017.6240

    Figure Lengend Snippet: TNF-α induced cell proliferation of RAECs. (A) Time-course and dose-response of RAEC proliferation following treatment with TNF-α. (B) Number of viable cells at 48 h following treatment with various concentrations of TNF-α. RAECs were seeded in a 96-well plate and were treated with various doses of TNF-α for 48 h; the number of viable cells was determined at the end of the experiment. Data are presented as the mean ± standard deviation of 6–10 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.

    Article Snippet: Levels of VEGF in the cell culture media were determined by electrochemiluminescence using an MSD ® 96-Well Multi-Array Rat VEGF Assay kit (cat. no. L45RA-1; Meso Scale Diagnostics LLC, Rockville, MD, USA).

    Techniques: Standard Deviation, Control

    TNF-α enhanced migratory ability of RAECs. (A) Migration was detected using a Transwell assay (magnification, ×100). (B) Compared with the control group, the migratory ability of RAECs was significantly increased in the TNF-α conditioned medium group. A concentration of 10 ng/ml TNF-α was used for the migration analysis. The control group was incubated in endothelial cell medium. Data are presented as the mean ± standard deviation of 6 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.

    Journal: Molecular Medicine Reports

    Article Title: Slit2 suppresses endothelial cell proliferation and migration by inhibiting the VEGF-Notch signaling pathway

    doi: 10.3892/mmr.2017.6240

    Figure Lengend Snippet: TNF-α enhanced migratory ability of RAECs. (A) Migration was detected using a Transwell assay (magnification, ×100). (B) Compared with the control group, the migratory ability of RAECs was significantly increased in the TNF-α conditioned medium group. A concentration of 10 ng/ml TNF-α was used for the migration analysis. The control group was incubated in endothelial cell medium. Data are presented as the mean ± standard deviation of 6 individual samples of independent triplicate experiments. *P<0.05 vs. control group. RAECs, rat aortic endothelial cells; TNF-α, tumor necrosis factor-α.

    Article Snippet: Levels of VEGF in the cell culture media were determined by electrochemiluminescence using an MSD ® 96-Well Multi-Array Rat VEGF Assay kit (cat. no. L45RA-1; Meso Scale Diagnostics LLC, Rockville, MD, USA).

    Techniques: Migration, Transwell Assay, Control, Concentration Assay, Incubation, Standard Deviation