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NULL OR EMPTY CART
Our ViewPlate microplates are engineered for bottom reading systems and high content imaging. This high quality microplate can be utilized in your cell based assay for superior results.
Poly-lysine is a synthetic positively-charged polymer, existing as two enantiomers: Poly-D-lysine (PDL) and Poly-L-lysine (PLL). Adherence of certain cell types to poly-lysine-coated surfaces is based on the electrostatic interaction of the poly-D-lysine polycation with the negative charges of the cell membrane. Use of poly-lysine coatings on plate surfaces can help mediate the negative charges of the cell membrane and the negative charge of the surface. Both PDL and PLL are commonly used however PDL is not degraded by cellular proteases and is therefore often the preferred choice. As Poly-lysine is a synthetic protein, it does not influence the signaling pathways of the cells and is completely free of any animal contaminants. Almost all cell types will adhere to Poly-lysine coated plate bottoms.
Leveraging years of assay and instrument experience in plate detection, Revvity designs better microplates for better performance that guarantees better results for all Revvity applications.
Well format: 96-well
Description | Specification |
---|---|
Number of Rows | 8 |
Number of Columns | 12 |
Well volume | 360 µL |
Recommended working volume | 80 µL- 350 µL |
Height (mm) | 14.61 |
Length (mm) | 127.81 |
Width (mm) | 85.65 |
Well diameter (mm) | 6.1 |
Well depth (mm) | 11.4 |
A1 to top offset (mm) | 11.3 |
A1 to side offset (mm) | 14.3 |
Well-to-well spacing (mm) | 9 |
Automation Compatible | Yes |
---|---|
Coating Treatment | Poly-D lysine (PDL) |
Color | Black/Clear Bottom |
Detection Method | Luminescence, Fluorescence |
Format | Microplates |
Material | Polystyrene |
Product Brand Name | ViewPlate |
Shipping Condition | Ambient |
Sterile | Aseptic |
Unit Size | Case of 40 |
Wells Number | 96 well plate |
We have shown here that signal intensity for the selected catalog aequorin cell lines is strong enough to allow its measurement by the non-luminescence dedicated FLIPR