CytoSelect™ 48-well Cell Adhesion Assay (ECM Array, Colorimetric)

Catalog No. ABIN2344825

Product Details

Reactivity: Mammalian

Detection Method: Colorimetric

Application: Cellular Assay (CA)

Brand: CytoSelect™

Sample Type: Serum, Cell Samples

Analytical Method: Quantitative

Characteristics: The CytoSelect™ Cell Adhesion Assay Kit provides a rapid, quantitative method for evaluating cell adhesion. The kit contains sufficient reagents for the evaluation of 48 samples (40 ECM protein-coated wells, 8 BSA-coated wells).

Components:

1. ECM Adhesion Plate : One 48-well plate containing 40 ECM protein-coated wells and 8 BSA-coated wells (see layout below). FN, Collagen IV and Fibrinogen are from human, Laminin I is from Mouse and Collagen I is from Bovine.
2. Cell Stain Solution : One Bottle - 10.0 mL
3. Extraction Solution : One Bottle - 10.0 mL

Material not included:

1. Cell culture medium
2. Serum free medium, such as DMEM containing 0.5 % BSA, 2 mM CaCl2 and 2 mM MgCl2
3. Cell culture incubator (37 °C, 5 % CO2 atmosphere)
4. 1X PBS containing 2 mM CaCl2 and 2 mM MgCl2
5. Light microscope
6. 96-well microtiter plate
7. Microtiter plate reader

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Comment:

• Full quantitation of cell adhesion with no manual cell counting
• Plates precoated with a uniform substrate layer of a single ECM protein in each row: Collagen I, Collagen IV, Fibrinogen, Fibronectin, and Laminin

Plate: Pre-coated

Protocol: The CytoSelect™ Cell Adhesion Assay Kit utilizes an ECM protein-coated 48-well plate (see Adhesion Plate Layout below). First, cells are seeded onto the coated substrate, where the adherent cells are captured. Next, unbound cells are washed away, and the adherent cells are fixed/stained. Finally, the stain is extracted and quantified colorimetrically.

Assay Procedure:

1. Under sterile conditions, allow the ECM Adhesion Plate to warm up at room temperature for 10 minutes.
2. Prepare a cell suspension containing 0.1-1.0 x 106 cells/mL in serum free media. Agents that inhibit or stimulate cell adhesion can be added directly to the cell suspension.
3. Add 150 μL of the cell suspension to the inside of each well (BSA-coated wells are provided as a negative control).
4. Incubate for 30-90 min in a cell culture incubator.
5. Carefully discard or aspirate the media from each well (Note: Do not allow wells to dry). Gently wash each well 4-5 times with 250 μL PBS. 3
6. Aspirate the PBS from each well and add 200 μL of Cell Stain Solution. Incubate for 10 minutes at room temperature.
7. Discard or aspirate the Cell Stain Solution from the wells. Gently wash each well 4-5 times with 500 μL deionized water.
8. Discard the final wash and let the wells air dry.
9. Add 200 μL of Extraction Solution per well, and then incubate 10 minutes on an orbital shaker.
10. Transfer 150 μL from each extracted sample to a 96-well microtiter plate and measure the OD 560nm in a plate reader.

Restrictions: For Research Use only

Handling

Storage: 4 °C

Storage Comment: Store all kit components at 4°C.

References

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Target Details

Background: Cell adhesion is a complex process involved in embryogenesis, migration/invasion, tissue remodeling, and wound healing. To perform these processes, cells adhere to extracellular matrix components (via adhesion receptors), forming complexes with components of the cytoskeleton that ultimately affect cell motility, differentiation, proliferation, and survival.