| Product name | Protein Quantification Kit (Bradford Assay) |
| Applications notes | Abbkine Protein Quantification Kit (Bradford Assay) provides a simple and rapid procedure for determining the concentration of protein in samples. The method utilizes an improved Coomassie blue G reagent which forms a blue complex in the presence of protein. When coomassie dye binds protein in an acidic medium, an immediate shift in absorption maximum occurs from 465nm to 595nm with a concomitant color change from brown to blue. The intensity of the blue complex is proportional to the amount of protein in the sample. |
| Detection method | Colorimetric |
| Alternative | Coomassie |
| Kit components | • Coomassie Assay Reagent • Albumin Standard (BSA) |
| Features & Benefits | • Time saving—almost immediate color development. • Compatible—unaffected by most chemical substances. The concentration of mercaptoethanol and dithiothreitol in the samples can reach 1mM and 5 mM respectively. • Broad range—working range from 50 to 1000 µg/ml. |
| Calibration range | 50-1000 µg/ml |
| Limit of detection | 25 µg/ml |
| Usage notes | Due to the influence of high concentration detergent, it is necessary to ensure that the concentration of SDS is lower than 0.1 %, Triton X-100 is lower than 0.1 % and Tween 20, 60, 80 is lower than 0.06 % in the sample. |
| Storage instructions | The unopened kit should be stored at 2 - 8°C. After opening, please store refer to protocols. |
| Shipping | Gel pack with blue ice. |
| Precautions | The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product. |
| Background | The Bradford assay, a colorimetric protein assay, is based on an absorbance shift of the dye Coomassie Brilliant Blue G-250. The Coomassie Brilliant Blue G-250 dye exists in three forms: anionic (blue), neutral (green), and cationic (red). Under acidic conditions, the red form of the dye is converted into its blue form, binding to the protein being assayed. If there's no protein to bind, then the solution will remain brown. The cationic (unbound) form is green / red and has an absorption spectrum maximum historically held to be at 465 nm. The anionic bound form of the dye which is held together by hydrophobic and ionic interactions, has an absorption spectrum maximum historically held to be at 595 nm. The increase of absorbance at 595 nm is proportional to the amount of bound dye, and thus to the amount (concentration) of protein present in the sample. |
| Alternative | Coomassie |
Fig. Protein Quantification Kit (Bradford Assay) standard curve
Author：Charoensin, Suphachai, and Suwatsak Dansakda. Publication name：Molecules IF：5.5
Author：Y Gao, J Xu, C Tang Publication name：Parasitology Research IF：2.36
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1.The species of antibody reactivity should be the sample species that can be matched normally after Abbkine R&D experts have passed strict scientific verification. If your sample is not within the range of reactivity, in order to improve the efficiency and results of your experiment, it is not suggested to try other species. Otherwise, it may lead to sample mismatch and affect the effect of your experiment.
2.Please aliquot the antibody received as soon as possible and store it at -20℃, avoid repeated freezing and thawing, and use it within one year.
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