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Bradford Protein Assay Calculator
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PM Lab Suite·Research Tool

Bradford Protein Assay Calculator

Generate a Bradford assay calibration curve and calculate unknown protein concentrations from absorbance measurements.

Input
Compute
Output
Interpret
Evidence

Input & Computation

Layer 1 + 2

This is a research calculator, not a clinical diagnostic tool. Build a standard curve for each assay run, review replicate CV and R\u00b2, and use only the concentration range validated for your specific reagent and protocol.

Assay Configuration

Interpretation Guide

Layer 3 + 4

Curve Models

Linear: y = mx + b
Quadratic: y = ax\u00b2 + bx + c
Unknown: x = (y \u2212 b) / m (linear) or root selection (quadratic)

Replicate Statistics

Mean = \u03a3x\u1d62 / n
SD = \u221a(\u03a3(x\u1d62 \u2212 x\u0304)\u00b2 / (n\u22121))
CV% = (SD / x\u0304) \u00d7 100

Evidence & References

Layer 5
1

Bradford MM (1976)

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72(1–2):248–254.

2

Bio-Rad

Bradford Protein Assay guidance and protocol documentation. Application notes for Coomassie Brilliant Blue G-250 based protein quantification.

Research calculator \u2014 not a clinical diagnostic tool. Linear: y = mx + b. Quadratic: y = ax\u00b2 + bx + c. Unknowns solved by inverse interpolation within the calibration range. R\u00b2 is a fit indicator, not proof of assay validity.

PM Lab Suite

Clinical Laboratory Intelligence Platform

Input— Structured inputs & validation
Compute— Validated formulas
Output— Critical value highlighting
Interpret— Clinical/lab relevance
Evidence— Guideline references

When to Use

  • Quantifying protein concentration from Bradford (Coomassie) absorbance readings at 595 nm
  • Building a standard curve with BSA or gamma globulin standards
  • Calculating unknown sample concentrations with dilution factors
  • Reviewing replicate CV and calibration R² before reporting results

Common Pitfalls

  • Protein-to-protein dye response differs — results depend on the selected standard
  • Detergents and other substances may interfere with Bradford assays
  • A high R² alone does not establish assay acceptability
  • Samples outside the calibration range should be diluted or re-assayed
  • Blank correction and dilution factors must reflect the actual experimental procedure