| Field | Specification |
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Product Overview
The 96-Well Cationic Protein-Binding Plates bind positively charged proteins. Proteins bound to the plate often keep their native conformation and their catalytic or binding activity, so a second molecule that needs the native structure can still recognize the bound protein.
The plates can be used for ELISA and for studies of protein-protein, protein-peptide, protein-DNA and protein-RNA interactions. The bound second molecule is detected by biochemical, biophysical or immunological methods.
Each pack contains 4 plates. Black plates give a low background for fluorescence detection. Transparent plates are for detection by light absorbance.
Example data: binding signal on a DNA-binding plate (left) and a protein-binding plate (right).
Product Description
| Option | Black (fluorescence detection) | Transparent (absorbance detection) |
|---|---|---|
| Catalog # | CPP96B | CPP96T |
| Plate Color | Black | Transparent |
| Detection | Fluorescence | Light absorbance |
| Contents | 4 plates | 4 plates |
Specifications
| Format | 96-well plates |
|---|---|
| Plate Color | Black or transparent (two options; see Product Description) |
| Pack Size | 4 plates per pack |
| Material | Polystyrene |
| Binds | Positively charged proteins |
| Catalog # | CPP96B, CPP96T |
| Storage | Please contact us to confirm storage conditions. |
| Shipping | Shipped at room temperature. |
Protocol Outline
- Add 200 µl of 0.5-1 mg/ml protein in a low-salt buffer (10 mM buffer, 10 mM NaCl, 0.01% Tween-20, 1 mM EDTA) to each well and incubate at 4°C overnight, then rinse.
- Block with 300 µl of blocker for 30 min: 1% BSA when the second molecule is a protein, or 1× Nucleic Acid Binding Blocker when it is a nucleic acid.
- Add 200 µl of the second molecule in low-salt buffer and incubate for 1 hour, then rinse.
- Detect the bound second molecule, for example by enzyme activity, a fluorescent or radioactive label, or SYBR Green fluorescence (Ex 485 nm / Em 535 nm) for nucleic acids.
The full ProFoldin protocol “Protein-binding Plates” is linked under Documents.
Notes
- The Nucleic Acid Binding Blocker used for nucleic acid partners is sold separately.
- The second molecule concentration depends on its binding affinity; about 0.1 mg/ml is typical for proteins, lower for antibodies, and micromolar for DNA oligos.
Safety & Handling
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