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Collagen I Cell Adhesion
Assay
48 assays
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| Catalog Number: 8008 |
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Introduction
Cell adhesion plays an important role in cellular communication
and regulation, and is of fundamental importance in the development
and maintenance of tissues. Collagen I, a major structural component
of extracellular matrices, is an excellent substrate for the culture
of many different cell types. The ScienCell Collagen I Cell
Adhesion Assay is designed for the rapid, quantitative and reliable
measurement of cell adhesion to collagen I. The kit includes a 48-well
plate pre-coated with collagen I, as well as BSA (bovine serum albumin)
as negative controls (see plate format in Figure 1). Cells are cultured
in the pre-coated wells for a desired period of time, then unbound
cells are washed away, and the adhered cells are fixed and stained,
followed by an extraction step which leads to dye elution from stained
cells into supernatant. Thus cell adhesion can be quantified using
a colorimetric ELISA plate reader at 595 nm.
Kit components
| Cat.
No. |
Item / Vial
|
Name |
Quantity
|
Storage
|
| 8008a |
1
|
Collagen I & BSA coated plate |
48-well
|
4°C
|
| 8008b |
1
|
Staining solution |
10 ml
|
4°C
|
| 8008c |
1
|
Extraction soulution |
10 ml
|
4°C
|
Quality Control
Serial diluted Human Pulmonary Fibroblasts (Cat. No. 3300, ScienCell)
are cultured in the pre-coated 48-well plate. A linear relationship
can be observed between signals produced (OD590nm) and the number
of cells, as shown in Figure 2.
Procedure
1. Under sterile conditions, allow the pre-coated 48-well plate
to warm to room temperature and rinse once with PBS.
2. Seed cells of interest into the 48-well plate and culture for
a desired period of time (at least 30-90 minutes) at 37°C.
3. After the culture is done, remove culture medium and rinse cells
with PBS for 3-5 times.
4. Add 200 µl/well of freshly diluted 0.1% glutaraldehyde
in PBS, fix for 10 minutes at room temperature. Then discard fixing
solution and rinse cells 3 times with PBS.
5. Add 200 µl/well of Staining Solution; incubate for 30 minutes
at room temperature on an orbital shaker.
6. After the staining is done, rinse plate with DI water 3-5 times,
invert plate onto paper tower to drain water residue and leave the
plate in air for dry.
7. Add 200 µl/well of Extraction Solution, incubate for 3-5
minutes and read OD595nm using an ELISA plate reader.
Table 1. Layout of the pre-coated plate
|
|
1
|
2
|
3
|
4
|
5
|
6
|
7
|
8
|
|
A
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
|
B
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
|
C
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
|
D
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
|
E
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
Collagen
|
|
F
|
BSA
|
BSA
|
BSA
|
BSA
|
BSA
|
BSA
|
BSA
|
BSA
|
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