CytoSelect™ 48-well Cell Adhesion Assay (Fibronectin, Fluorometric)

N° du produit ABIN2344816

Aperçu rapide pour CytoSelect™ 48-well Cell Adhesion Assay (Fibronectin, Fluorometric) (ABIN2344816)

Reactivité: Humain

Méthode de détection: Fluorometric

Application: Cellular Assay (CA)

Type d'échantillon: Serum, Cell Samples

Analytical Method: Quantitative

Détail du produit

Marque: CytoSelect™

Attributs du produit: 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 Human Fibronectin-coated wells, 8 BSA- coated wells).

Ingrédients:

1. Fibronectin Adhesion Plate : One 48-well plate containing 40 Human Fibronectin-coated wells and 8 BSA-coated wells (see layout below)
2. 4X Lysis Buffer : One Bottle - 10.0 mL
3. CyQuant® GR Dye : One tube - 50 μL 2

Matériel non inclus:

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 plate suitable for a fluorescence plate reader
7. Fluorescence plate reader

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

• Full quantitation of cell adhesion with no manual cell counting
• Plates precoated with uniform substrate layer of Fibronectin

Plaque: Pre-coated

Protocole: The CytoSelect™ Cell Adhesion Assay Kit utilizes a Fibronectin-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 removed with consecutive washes. Finally, the adherent cells are lysed and subsequently detected with CyQuant® GR Dye.

Procédure de l'essai:

1. Under sterile conditions, allow the Fibronectin 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. 3
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.
6. Prepare sufficient 1X Lysis Buffer/CyQuant® GR dye solution for all samples by diluting the dye 1:300 in Lysis Buffer (for example, add 4 μL dye to 300 μL of 4X Lysis Buffer and 900 μL of dH2O).
7. Add 200 μL of 1X Lysis Buffer/CyQuant® GR dye solution to each well containing cells. Incubate 20 minutes at room temperature with shaking.
8. Transfer 150 μL of the mixture to a 96-well plate suitable for fluorescence measurement. Read fluorescence with a fluorescence plate reader at 480 nm/520 nm.

Restrictions: For Research Use only

Stockage

Stock: 4 °C

Stockage commentaire: Store all kit components at 4°C.

Détail du antigène

Sujet: 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.