BCA Protein Assay Kit

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純度（試験方法）:

別名:

• BCAタンパク質アッセイキット
• BCAタンパク質定量キット
• BCA Protein Quantitation Kit

製品書類：

SDS | 規格表 | 試験成績書・各種証明書 | 分析チャート

基本情報 | 規格値・物性値 | 法規情報 | 利用例・文献

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包装単位	価格	埼玉県(川口)倉庫	兵庫県(尼崎)倉庫	その他の倉庫	出荷情報
1KIT	¥14,500	36	埼玉県倉庫より即日*発送可能です	お問い合わせ	出荷シミュレーション

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Product Information

• Components : BCA Reagent A: 250 mL, BCA Reagent B: 25 mL
• Size : 125 tests (Cuvette). 1250 tests (96-well plate).

Description

• The BCA protein assay is a highly sensitive colorimetric method used to quantify protein concentration. It utilizes the color reaction of bicinchoninic acid with copper ions, which themselves have been reduced by peptide bonds in proteins, allowing quantification via absorbance measurement at 562 nm. Its resistance to common interfering substances makes it suitable for use with most biological samples.

Storage

• Store at room temperature. Use within 1 year.

Note

• For Research Use Only. Not for Diagnostic or Therapeutic Use.

Compatible substance concentrations in protein sample

• See the pdf file in this link.

Protocol (96-well plate)

• 1. Mix Reagent A and Reagent B at a ratio of 50:1 to prepare a working solution.
  2. Dispense 25 µL of protein standards (e.g., a two-fold serially diluted BSA solution series starting at 2 mg/mL), blank (0 mg/mL), and samples into appropriate wells.
     Caution: Samples falling outside the calibration range must be measured again with appropriate dilutions.
  3. Add 200 µL of the working solution to each well and mix gently.
  4. Incubate at 37 °C for 30 minutes.
  5. After incubation, remove any bubbles by gently tapping or shaking the plate and measure the absorbance at 562 nm (acceptable range: 540-570 nm).
  6. Subtract the blank absorbance from all readings (blank correction).
  7. Plot the blank-corrected absorbance values of the standard curve against protein concentration to obtain a regression equation.
  8. Use this equation to calculate the protein concentration of each sample.

Protocol (Cuvette)

• 1. Mix Reagent A and Reagent B at a ratio of 50:1 to prepare a working solution.
  2. Dispense 2.0 mL of the working solution into each of an appropriate number of sample tubes.
  3. Add 100 µL of protein standards (e.g., a two-fold serially diluted BSA series starting at 2 mg/mL), blank (0 mg/mL), and samples to the respective tubes.
     Caution: Samples falling outside the calibration range must be measured again with appropriate dilutions.
  4. Mix by vortexing or pipetting until thoroughly combined.
  5. Incubate at 37 °C for 30 minutes.
  6. After incubation, ensure that no bubbles are present in the light path of the cuvette, and measure the absorbance at 562 nm.
  7. Subtract the blank absorbance from all readings (blank correction).
  8. Plot the blank-corrected absorbance values of the standard curve against protein concentration to obtain a regression equation.
  9. Use this equation to calculate the protein concentration of each sample.