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ECM671

QCM Gelatin Invadopodia Assay (Red)

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About This Item

UNSPSC Code:
12161503
NACRES:
NA.76
eCl@ss:
32161000
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technique(s)

cell migration: suitable

detection method

fluorometric

Quality Level

Application

The EMD Millipore QCM Gelatin Invadopodia Assay (Red) provides the reagents necessary for affixing a thin, uniform layer of Cy3-labeled gelatin to a glass culture substrate, allowing for rapid detection of matrix degradation (Artym et al., 2009, Xu et al., 2009). A poly-L-lysine coating is first adsorbed to the glass substratum. The substrate is then treated with a dilute glutaraldehyde solution to bi-functionally “activate” the surface for further protein binding. Subsequent incubation of the surface with fluorescent gelatin allows covalent coupling between the poly-L-lysine and gelatin via reactive aldehyde (-CHO) groups. The fluorescently-coated glass is now prepared for cell culture by disinfection with 70% ethanol, followed by quenching of free aldehydes with amino acid-containing growth medium. Upon completion of fluorescent substrate preparation, cell types of interest may be seeded onto the gelatin surface for a desired amount of time. Depending on cell type, degradation may occur within a few to several hours. Treatment compounds of interest may also be introduced within the culture period.

With EMD Millipore′s QCM Gelatin Invadopodia Assay (Red), degraded areas of gelatin, now devoid of fluorescence, may be microscopically visualized and quantified using image analysis software algorithms. The assay also provides fluorescent FITC-phalloidin and DAPI, for visualization of cytoskeletal F-actin and nuclei, respectively, to allow co-localization of degradation with cellular features. Potential activators or inhibitors of invadopodia formation may be investigated for their influence on the degree and frequency of matrix degradation, and the assay may be further combined with immunocytochemical staining for other molecules of interest in pathway studies.

Disclaimer

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.

Other Notes

Cy3-Gelatin, 4X: One vial containing 0.5 mL Unlabeled Gelatin, 4X: One vial containing 2 mL DAPI: One vial containing 100 µL at 100 µg/mL in water Poly-L-Lysine, 2X: One vial containing 5 mL Glutaraldehyde, 16X: One vial containing 1 mL FITC-Phalloidin: One vial containing 20 µg

Packaging

Enough Reagents for 4 x 8-well Chamber Slides (32 assays)

Preparation Note

Store Cy3-Gelatin, Unlabeled Gelatin, Poly-L-Lysine and DAPI at 2-8°C. Store Glutaraldehyde and FITC-Phalloidin at -20°C. Use all reagents within 4 months from date of receipt.

Legal Information

Cy3 is a trademark of Cytiva

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

supp_hazards

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Regulatory Information

监管及禁止进口产品
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Related Content

QCM™ Gelatin Invadopodia Assays provide optimized materials and protocols to enable reproducible analysis of invadopodia in invasive tumor cells (Catalog No. ECM670 for green fluorescence, Catalogue No. ECM671 for red fluorescence). Reagents are provided for coating glass culture surfaces with fluorescent matrix and for colocalizing the actin cytoskeleton and nuclei with invadopodial degradation sites. This assay may also be used for assessing the activity of inhibitors and promoters of invadopodia formation and function. Furthermore, different cell types and individual cells in heterogeneous populations may be analyzed for invasive potential. Finally, the assay kits provide troubleshooting suggestions, recommendations for coating on multiple substrate formats, and example studies in several assay systems (e.g., various cell types, time-course studies, degradation modulation).

Cell migration is stimulated and directed by interaction of cells with the extracellular matrix (ECM), neighboring cells, or chemoattractants. Cell migration participates in morphogenic processes, wound healing and tumor metastasis. Specifically, inhibiting tumor invasion by blocking tumor cell chemotaxis has been a major focus of research. Tumor cell invasion, marked by degradation of ECM, is also directly correlated with metastatic potential.

"Recognizing both the tremendous opportunities and the challenges facing cancer research, we are dedicated to developing and refining tools and technologies for the study of cancer. With our comprehensive portfolio, including the Upstate®, Chemicon®, and Calbiochem® brands of reagents and antibodies, researchers can count on dependable, high quality solutions for analyzing all the hallmarks of cancer."

Key Steps in Tumor Metastasis

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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