ProLite™ FAST Blue Protein Gel Stain *200 Gels*
Price | |
Catalog Number | |
Unit Size | |
Quantity |
Telephone | 1-800-990-8053 |
Fax | 1-800-609-2943 |
sales@aatbio.com | |
International | See distributors |
Bulk request | Inquire |
Custom size | Inquire |
Shipping | Standard overnight for United States, inquire for international |
Solvent | DMSO |
H-phrase | H303, H313, H333 |
Hazard symbol | XN |
Intended use | Research Use Only (RUO) |
R-phrase | R20, R21, R22 |
Storage | Freeze (< -15 °C); Minimize light exposure |
Overview | SDSProtocol |
Platform
Gel Imager
Excitation | Coomassie Blue Filter Set |
Emission | Coomassie Blue Filter Set |
Components
Example protocol
PREPARATION OF STOCK SOLUTIONS
Prepare a stock solution by adding 500 µL of DMSO into the vial of ProLite™ FAST Blue Protein Gel Stain (Component A).
Note: Any unused stock solution should be divided into single-use aliquots and stored at ≤-20 °C for two weeks. Avoid repeated freeze-thaw cycles and minimize light exposure.
Note: The 500 µL stock solution can effectively stain up to 200 gels, with each gel containing 10 wells.
PREPARATION OF WORKING SOLUTION
Prepare a working solution by adding 50 µL of the ProLite™ FAST Blue Protein Gel Stain stock solution to 1 mL of Staining buffer (Component B).
Note: Any unused working solution should be divided into single-use aliquots and stored at ≤-20 °C for two weeks. Avoid repeated freeze-thaw cycles and minimize light exposure.
SAMPLE EXPERIMENTAL PROTOCOL
Add 0.25 µL of the ProLite™ FAST Blue Protein Gel Stain stock solution to 10 µL of the protein lysate.
Note: The dye volume can be adjusted based on the total volume and protein concentration used in the lysate.
Incubate the mixture at room temperature for 15 to 60 minutes, protected from light.
Add the loading dye to the protein lysate as per the manufacturer's guidelines.
Load the samples onto the gel and run.
Following the completion of the gel run, the samples should be visibly present within the gel.
Images
Application notes
A Novel Fluorescent Probe for Imaging and Detecting Hydroxyl Radical in Living Cells
A Novel NO Wash Probeniceid-Free Calcium Assay for Functional Analysis of GPCR and Calcium Channel Targets
Biotin Labeling Molecules and Their Biological Applications
Buccutite™ Bioconjugation Technology
FAQ
What are the differences between calcium ion indicators: Cal 520, Cal 520FF, and Cal 520N?
How do I make an AM ester stock solution?
Can we fix cells with glutaraldehyde and then stain with fluorescent phalloidin?
What is the difference between FluoroQuest Anti-fading Kit I and FluoroQuest Anti-fading Kit II?