产品
- 产品介绍
Kit Contents: | storage | |||
| Extraction Times | 500 | 2500 | RT |
Ⅰ | Working Reagent | 100 ml | 500 ml | RT |
Ⅱ | BSA(5 mg/ml) | 2 ml | 10 ml | -20°C |
The Bradford assay relies on the binding of staining Coomassie Blue G250 to protein in acid medium and the complexing exhibiting a maximum absorbance at 595 nm that is nearly linear with increasing protein concentrations over a wide working range. According to highly sensitivity and simple to use, the Bradford protein assay is adopted by laboratories and companies, and becomes one of the prior protein quantitative methods as well as the BCA assay.
The Fine Bradford Protein Assay Kit has the characteristics of high sensitivity, light background and significant color difference, and the measured of protein in low concentration can be intuitive and convenient.
" } } [1568013276]=> array(1) { ["two_columns_with_html"]=> array(2) { ["title"]=> string(9) "Procedure" ["content"]=> string(1731) "1.96-Microplate Procedure
(1) Prepare the Standard Reagent. Dilute the 5 mg/ml BSA Standard into lateral concentrations of 0, 0.25, 0.5, 0.75, 1, 1.5 mg/ml. The BSA dilutions can be frozen and stored at –20℃，and thawed and warmed to room temperature when used.
(2) Mark the wells with Standard or Test. Add at least 10 µl of the diluted Standard Reagent to each Standard well and add equal volume of testing samples each Test well.
(3) Add all the wells with 200 µl Working Reagent and waggle slightly for mixing.
(4) Measure the absorbance at 595 nm on a plate reader. Subtract the average absorbance reading of at least 3 blank wells. Draw a standard curve by plotting absorbance reading for each BSA standard versus its concentration. Use the standard curve to determine the protein concentration of each unknown sample.
2.Test Tube Procedure
(1) Prepare the Standard Reagent. Dilute the 5 mg/ml BSA Standard into lateral concentrations of 0, 0.25, 0.5, 0.75,
1, 1.5 mg/ml. The BSA dilutions can be frozen and stored at –20℃，and thawed and warmed to room temperature when used.
(2) Mark the tubes with Standard or Test. Add at least 30 µl of the diluted Standard Reagent to each Standard tube and add equal volume of testing samples each Test tube.
(3) Add all the tubes with 1 ml Working Reagent and waggle slightly for mixing.
(4) Measure the absorbance at 595 nm with a spectrophotometer. Subtract the average absorbance reading of at least 3 blank tubes. Draw a standard curve by plotting absorbance reading for each BSA standard versus its concentration. Use the standard curve to determine the protein concentration of each unknown sample.
" } } [1568013326]=> array(1) { ["two_columns_with_text"]=> array(3) { ["search"]=> string(1) "0" ["title"]=> string(30) "Additional Testing Information" ["content"]=> string(285) "Using the same protein with known concentration to prepare Standard Reagent can enhance the accuracy of concentration determining, e.g. determine the concentration of serum protein with Standard Reagent of BSA, or determine the concentration of antibodies with Standard Reagent of IgG." } } [1568013297]=> array(1) { ["two_columns_with_html"]=> array(2) { ["title"]=> string(4) "Note" ["content"]=> string(466) "1. Although reagents stored at 4℃ rarely precipitate, a small amount of precipitation is acceptable and can be resolved by reversing the container.
2. Reagents of Bradford testing is highly acid. Please wear lab coat and gloves during assays for safety considerations.
3. Fine Bradford Protein Assay Kit is intolerant with detergent reagents. If detergent reagents are inevitable, FineTest product- Fine BCA Protein Assay Kit is available(K001).
" } } }- Product name
Bradford Protein Assay Kit
- Product code
K002
- Kit Contents
Kit Contents:
storage
Extraction Times
500
2500
RT
Ⅰ
Working Reagent
100 ml
500 ml
RT
Ⅱ
BSA(5 mg/ml)
2 ml
10 ml
-20°C
- Storage
The kit should be protected from light and stored at-20℃ for long-term storage. The kit should be warmed to room temperature before used for the best testing sensitivity.
- Introduction
The Bradford assay relies on the binding of staining Coomassie Blue G250 to protein in acid medium and the complexing exhibiting a maximum absorbance at 595 nm that is nearly linear with increasing protein concentrations over a wide working range. According to highly sensitivity and simple to use, the Bradford protein assay is adopted by laboratories and companies, and becomes one of the prior protein quantitative methods as well as the BCA assay.
The Fine Bradford Protein Assay Kit has the characteristics of high sensitivity, light background and significant color difference, and the measured of protein in low concentration can be intuitive and convenient.
- Procedure
1.96-Microplate Procedure
(1) Prepare the Standard Reagent. Dilute the 5 mg/ml BSA Standard into lateral concentrations of 0, 0.25, 0.5, 0.75, 1, 1.5 mg/ml. The BSA dilutions can be frozen and stored at –20℃，and thawed and warmed to room temperature when used.
(2) Mark the wells with Standard or Test. Add at least 10 µl of the diluted Standard Reagent to each Standard well and add equal volume of testing samples each Test well.
(3) Add all the wells with 200 µl Working Reagent and waggle slightly for mixing.
(4) Measure the absorbance at 595 nm on a plate reader. Subtract the average absorbance reading of at least 3 blank wells. Draw a standard curve by plotting absorbance reading for each BSA standard versus its concentration. Use the standard curve to determine the protein concentration of each unknown sample.
2.Test Tube Procedure
(1) Prepare the Standard Reagent. Dilute the 5 mg/ml BSA Standard into lateral concentrations of 0, 0.25, 0.5, 0.75,
1, 1.5 mg/ml. The BSA dilutions can be frozen and stored at –20℃，and thawed and warmed to room temperature when used.
(2) Mark the tubes with Standard or Test. Add at least 30 µl of the diluted Standard Reagent to each Standard tube and add equal volume of testing samples each Test tube.
(3) Add all the tubes with 1 ml Working Reagent and waggle slightly for mixing.
(4) Measure the absorbance at 595 nm with a spectrophotometer. Subtract the average absorbance reading of at least 3 blank tubes. Draw a standard curve by plotting absorbance reading for each BSA standard versus its concentration. Use the standard curve to determine the protein concentration of each unknown sample.
- Additional Testing Information
Using the same protein with known concentration to prepare Standard Reagent can enhance the accuracy of concentration determining, e.g. determine the concentration of serum protein with Standard Reagent of BSA, or determine the concentration of antibodies with Standard Reagent of IgG.
- Note
1. Although reagents stored at 4℃ rarely precipitate, a small amount of precipitation is acceptable and can be resolved by reversing the container.
2. Reagents of Bradford testing is highly acid. Please wear lab coat and gloves during assays for safety considerations.
3. Fine Bradford Protein Assay Kit is intolerant with detergent reagents. If detergent reagents are inevitable, FineTest product- Fine BCA Protein Assay Kit is available(K001).