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ECM200 QCM 3 µm Endothelial Cell Migration Assay Fibronectin, Colorimetric

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ECM200
1 kit  Sufficient for 12 assays
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      Overview

      Replacement Information

      Key Spec Table

      Detection Methods
      Fluorescent Colorimetric
      Description
      Catalogue NumberECM200
      Trade Name
      • QCM
      • Chemicon
      DescriptionQCM 3 µm Endothelial Cell Migration Assay Fibronectin, Colorimetric
      OverviewAlso available: Cell Comb™ Scratch Assay! Get biochemical data from a scratch assay! Click Here

      Introduction
      Angiogenesis is a fundamental process involving the growth of new blood vessels from pre-existing vessels. It is important in development and wound healing, as well as pathologic diseases such as diabetic retinopathy and cancer. During angiogenesis, endothelial cells need to move out of existing vessels, migrate into new areas, proliferate and assemble into new capillaries. The migration of endothelial cells is regulated by many angiogenic factors and anti-angiogenic factors. It is critical for researchers to understand the mechanisms of endothelial cell migration.

      Millipore's 3 μm QCM™ Endothelial Cell Migration Assay – Fibronectin, Colorimetric provides a quick and efficient system to study the ability of compounds to induce or inhibit endothelial cell migration. This assay also allows screening of pharmacological agents, evaluation of integrins or other adhesion receptors responsible for endothelial cell migration, analysis of gene function in transfected cells, and determination of ECM protein involvement in cell movement.

      This versatile assay permits counting of individual migratory cells, and, more importantly, allows quantitative analysis by optical density (OD) using a standard microplate reader. This convenient assay allows large scale screening and quantitative comparison of multiple samples and includes individual migration controls for each sample.
      Materials Required but Not Delivered1. Precision pipettes: sufficient for aliquoting cells.
      2. Harvesting buffer: EDTA or trypsin based cell detachment buffer, or other cell detachment formulations as optimized by individual investigators. Millipore’s ready-to-use non-mammalian detachment solution, Accutase™ (Cat. No. SCR005) can also be used.
      3. Endothelial cells (for example: HUVEC cells).
      4. Endothelium cell culture medium appropriate for subject cells, such as EGM-2 (Endothelial cell growth media-2)
      5. Quenching Medium: serum-free medium, such as DMEM, MEM etc containing 5% BSA. Must contain divalent cations (Mg 2+, Ca2+) sufficient for quenching EDTA in harvesting buffer.
      6. Sterile PBS or HBSS to wash cells.
      7. Distilled water
      8. (Optional) Chemoattractant or pharmacological agent added to culture medium.
      9. Low speed centrifuge and tubes for cell harvesting.
      10. CO2 incubator appropriate for subject cells.
      11. Hemocytometer or other means of counting cells.
      12. Trypan blue or equivalent viability stain.
      13. Microplate reader (540-570 nm detection) or spectrophotometer.
      14. Sterile cell culture hood
      15. (Optional) Graduated ocular (calibrated), or automated method for counting stained cells on a membrane.
      16. Shaker
      References
      Product Information
      Components
      • 1. Fibronectin Test Plate: One 24-well culture plate, containing 12 human FN-coated Boyden chambers, sufficient for the evaluation of 12 test samples.
      • 2. BSA Control Plate: One 24-well culture plate, containing 12 BSA-coated Boyden chambers, sufficient for the evaluation of 12 controls.
      • 3. Cell Stain Solution: One vial - 10 mL
      • 4. Extraction Buffer: One vial - 10 mL
      • 5. 24-Well Stain Extraction Plate
      • 6. 96-Well Stain Quantitation Plate
      • 7. Swabs: 50 ea
      • 8. Forceps: 1 pair
      Detection methodFluorescent Colorimetric
      Quality LevelMQ100
      Applications
      ApplicationThis QCM 3 μm Endothelial Cell Migration Assay – Fibronectin, Colorimetric is ideal for the study of endothelial cell migration in response to an angiogenic stimulus.
      Application NotesThe Millipore QCM™ 3 μm Endothelial Cell Migration Assay – Fibronectin, Colorimetric is ideal for the study of endothelial cell migration in response to an angiogenic stimulus. The quantitative nature of this assay is especially useful for large scale screening of pharmacologic agents. BSA-coated control chambers provide an appropriate migration control. The 3 μm pore size in this assay is optimal for endothelial cells such as HUVEC, but not sufficient for fibroblast migration. The Millipore QCM™ 3 μm Endothelial Cell Migration Assay – Fibronectin, Colorimetric assay is intended for research use only; not for diagnostic applications.
      Each kit provides sufficient materials for the evaluation of 12 samples.
      Biological Information
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Usage Statement
      • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
      Storage and Shipping Information
      Storage ConditionsStore kit materials at 2° to 8°C for up to their expiration date. Do not freeze.
      Packaging Information
      Material Size1 kit
      Material PackageSufficient for 12 assays
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Catalogue Number GTIN
      ECM200 04053252274657

      Documentation

      QCM 3 µm Endothelial Cell Migration Assay Fibronectin, Colorimetric MSDS

      Title

      Safety Data Sheet (SDS) 

      References

      Reference overviewPub Med ID
      Positive influence of AP-2alpha transcription factor on cadherin gene expression and differentiation of the ocular surface.
      Judith A West-Mays, Jeremy M Sivak, Steve S Papagiotas, Jennifer Kim, Timothy Nottoli, Trevor Williams, M Elizabeth Fini
      Differentiation; research in biological diversity  71  206-16  2003

      Show Abstract Full Text Article
      12694203 12694203

      Brochure

      Title
      Advancing cancer research: From hallmarks & biomarkers to tumor microenvironment progression
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      User Guides

      Title
      QCM™ 3 mm Endothelial Cell Migration Assay – Fibronectin, Colorimetric

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      Categories

      Life Science Research > Cell Analysis > Cell-based Assays > Cell Migration Assays