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Thermo Scientific™ Pierce™ BCA Protein Assay Reagent A

Description
Thermo Scientific™ Pierce BCA Protein Assay Kit remains one of the most popular protein quantitation methods worldwide.
Additional Information and Online Ordering
- A component of the Pierce BCA Protein Assay Kit
- Kit is a two-component, high-precision, detergent-compatible assay that is used for total protein concentration determination compared to a protein standard
- Pierce BCA reagents provide accurate determination of protein concentration with most sample types encountered in protein research
- The Pierce BCA assay can be used to assess yields in whole cell lysates, affinity-column fractions, purified proteins samples, as well as to monitor protein contamination in industrial applications
- Compared to most dye-binding methods, the BCA assay is affected much less by protein compositional differences, providing greater concentration accuracy
- Estimate visually or measure with a standard spectrophotometer or plate reader at 562 nm
- Exhibits less protein-to-protein variation than dye-binding methods (Bradford)
- Unaffected by typical concentrations of most ionic and non-ionic detergents
- Assay has a 30 min. incubation; much easier and four times faster than classical Lowry methods
- Linear working range for BSA of 20 to 2000 μg/mL
- Detect down to 5 μg/mL with the enhanced protocol
- Store at room temperature
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Specifications
Specifications
| Content And Storage | Store at room temperature. |
| Description | Pierce BCA Protein Assay Reagent A |
| Assay | BCA Assay |
| Detection Method | Colorimetric |
| Product Line | Pierce |
| Product Type | Protein Quantitation Assay |
| Specificity | Not Target-Specific |
| For Use With (Application) | Solution-based Detection, Absorbance |
| For Use With (Equipment) | Spectrophotometer, Microplate Reader |
| Quantity | 1 L |
Frequently Asked Questions (FAQs)
The choice of protein assay is dependent on preferences related to assay speed, accuracy and sensitivity, as well as interfering substances in the sample to be assayed. BCA has less protein-to-protein variation, is compatible with most detergents, and has larger working range. Pierce Bradford Plus Protein Assay Kit (Cat. No. 23236) is compatible with reducing sugars, is more sensitive and is faster and easier to use. For a comparison of different protein assays and compatible reagents, see our Tech Tip: Protein Quantitation Assay Compatibility Table (https://assets.thermofisher.com/TFS-Assets/LSG/Application-Notes/TR0068-Protein-assay-compatibility.pdf).
Reducing agents, copper chelators and solutions with very high buffering capacities will interfere with the BCA assay. Reducing agents reduce the copper and will produce a high background. Copper chelators bind the copper and prevent it from being detected by the BCA reagent. High-capacity buffers prevent the BCA from reaching its optimal alkaline pH. For a complete list of compatible substances, please refer to the BCA Protein Assay Kit product instructions.
For the Microplate Protocol the sample to working reagent (WR) ratio is 1:8 (25 µl sample plus 200 µl WR). If the sample amount is limited, a 1:20 ratio may be used (10 µl sample); in this case, however, the detection range of the assay will be limited to 125-2,000 µg/ml. For the Test Tube Procedure (Standard or Enhanced Protocols) the ratio is 1:20 (0.1 ml sample plus 2.0 ml WR). In the Micro BCA Assay Kit (for both Microplate and Test Tube Procedures), the ratio is 1:1 (1 part sample plus 1 part WR).
For the standard protocol, the detection range is 20-2,000 µg/ml. For the enhanced test tube protocol, the detection range is 5-250 µg/ml. The Micro BCA Protein Assay Reagent will detect 0.5-20 µg/ml of protein in the test tube assay and 1-20 µg/ml for the microplate assay.
There are several ways to adjust a sample to be compatible with the BCA Protein Assay: • Remove the interfering substance by dialysis or gel filtration. • If the starting protein concentration of the sample is high, dilute the sample to the point that the substance no longer interferes. • Eliminate interference by copper-chelating agents by increasing the amount of copper in the working reagent (use 4 ml or 6 ml of Reagent B/100 ml of Reagent A instead of the 2 ml of Reagent B/100 ml of Reagent A that is called for in the instructions). • Precipitate sample proteins with cold acetone or trichloroacetic acid (TCA).
For Research Use Only. Not for use in diagnostic procedures.
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