Protein Concentration Calculator
Convert between mg/mL, µg/mL, µM, nM, and Molarity (M) instantly
🧪 Calculate Protein Concentration
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What is Protein Concentration?
Protein concentration refers to the amount of protein present in a solution, typically measured in mass per volume (mg/mL, µg/mL) or molar units (M, µM, nM). Accurate protein concentration measurements are essential for biochemistry experiments, drug development, enzyme assays, and protein purification workflows.
Understanding protein concentration in different units allows researchers to:
- Prepare accurate dilutions for experiments
- Calculate enzyme kinetics and binding affinities
- Optimize protein crystallization conditions
- Standardize protocols across different laboratories
- Compare results with published literature
The key to converting between mass-based (mg/mL) and molar-based (µM, nM, M) concentrations is knowing the protein’s molecular weight, which represents the mass of one mole of the protein.
How to Calculate Protein Concentration
Understanding the Conversion Formulas
Converting protein concentrations requires understanding the relationship between mass concentration and molar concentration through molecular weight:
Step-by-Step Calculation Process
- Determine molecular weight: Find your protein’s molecular weight in daltons (Da) or kilodaltons (kDa). This information is usually available from protein databases or can be calculated from the amino acid sequence.
- Convert to base units: If needed, convert kDa to Da (1 kDa = 1000 Da). For calculations, 1 Da = 1 g/mol.
- Calculate molarity: First convert any concentration to molarity using the formula above.
- Convert to desired unit: Use the molarity value to calculate any other concentration unit.
Example Calculations
Example 1: Bovine Serum Albumin (BSA)
Given: BSA at 5 mg/mL, Molecular Weight = 66.5 kDa
Calculate µM concentration:
- Convert to molarity: M = (5 mg/mL × 1000) / 66,500 g/mol = 0.0000752 M
- Convert to µM: 0.0000752 M × 1,000,000 = 75.2 µM
Answer: 5 mg/mL BSA = 75.2 µM
Example 2: Antibody Solution
Given: IgG antibody at 100 nM, Molecular Weight = 150 kDa
Calculate mg/mL concentration:
- Convert nM to M: 100 nM / 1,000,000,000 = 0.0000001 M
- Calculate mg/mL: (0.0000001 × 150,000) / 1000 = 0.015 mg/mL
Answer: 100 nM IgG = 0.015 mg/mL = 15 µg/mL
Example 3: Enzyme Preparation
Given: Lysozyme at 250 µg/mL, Molecular Weight = 14.3 kDa
Calculate nM concentration:
- Convert to mg/mL: 250 µg/mL / 1000 = 0.25 mg/mL
- Calculate molarity: (0.25 × 1000) / 14,300 = 0.00001748 M
- Convert to nM: 0.00001748 × 1,000,000,000 = 17,483 nM
Answer: 250 µg/mL lysozyme = 17.48 µM = 17,483 nM
Common Protein Molecular Weights
| Protein | Molecular Weight | Common Application |
|---|---|---|
| Insulin | 5.8 kDa | Hormone research, diabetes studies |
| Lysozyme | 14.3 kDa | Enzyme assays, crystallography |
| Myoglobin | 17 kDa | Oxygen binding studies |
| Carbonic Anhydrase | 29 kDa | Enzyme kinetics |
| Ovalbumin | 45 kDa | Protein standard, immunology |
| BSA (Bovine Serum Albumin) | 66.5 kDa | Protein standard, blocking agent |
| IgG Antibody | 150 kDa | Immunoassays, therapeutics |
Why Molecular Weight Matters in Protein Calculations
Molecular weight is the critical variable that bridges mass-based and molar concentration measurements. Here’s why it’s essential:
1. Stoichiometry in Biochemical Reactions
Chemical reactions occur at the molecular level, not by mass. When studying enzyme-substrate interactions, antibody-antigen binding, or protein-protein interactions, you need to know the molar ratio of components. A 1:1 molar ratio doesn’t mean a 1:1 mass ratio if the molecules have different molecular weights.
2. Comparing Different Proteins
Two proteins at the same mass concentration (mg/mL) contain vastly different numbers of molecules if they have different molecular weights. For example, 1 mg/mL of a 10 kDa protein contains 10 times more molecules than 1 mg/mL of a 100 kDa protein. Molar units allow fair comparisons.
3. Kinetic Studies and Binding Assays
Enzyme kinetics parameters like Km, Kd, IC50, and EC50 are expressed in molar units because they represent molecular-level interactions. Converting your protein concentration to µM or nM is essential for these calculations.
💡 Pro Tip: Finding Molecular Weight
If you don’t know your protein’s molecular weight:
- Check UniProt database for characterized proteins
- Use ExPASy ProtParam to calculate from amino acid sequence
- Look at the manufacturer’s product sheet for commercial proteins
- Run SDS-PAGE with molecular weight markers
4. Dilution and Serial Dilution Planning
When preparing a dilution series for dose-response experiments, working in molar units ensures each dilution represents an accurate log-scale reduction in molecular concentration, not just mass.
Lab Tips & Common Mistakes
✅ Best Practices
1. Always Verify Molecular Weight
Don’t assume molecular weight from protein names alone. Post-translational modifications (glycosylation, phosphorylation) and fusion tags can significantly alter the molecular weight. Use the actual molecular weight of your specific protein construct.
2. Account for Protein Purity
If your protein is 80% pure, adjust your calculations accordingly. The concentration measurement might represent total protein, but only a fraction is your target protein.
3. Use Appropriate Measurement Methods
Different concentration measurement methods have different sensitivities:
- Bradford assay: 1-25 µg/mL range
- BCA assay: 20-2000 µg/mL range
- A280 absorbance: 50-5000 µg/mL range
- Lowry assay: 5-100 µg/mL range
⚠️ Common Mistakes to Avoid
Mistake 1: Confusing kDa and Da
Remember: 1 kDa = 1,000 Da. Always convert to the same unit before calculating. For molecular weight in g/mol, use Da (since 1 Da = 1 g/mol).
Mistake 2: Incorrect Unit Conversions
Pay attention to the factor of 1000 when converting between mg and µg, or between mL and L. Double-check your decimal places, especially when working with nM concentrations.
Mistake 3: Ignoring Buffer Components
Some buffer components can interfere with concentration measurements. BSA, detergents, and reducing agents can affect colorimetric assays. Use the same buffer for blanks and standards.
Mistake 4: Not Considering Protein Aggregation
Aggregated proteins may give inaccurate concentration readings. Always centrifuge protein solutions before measuring concentration if aggregation is suspected.
Quick Reference Guide
| Conversion | Multiply By | Example |
|---|---|---|
| M to µM | 1,000,000 | 0.00001 M = 10 µM |
| M to nM | 1,000,000,000 | 0.00001 M = 10,000 nM |
| µM to nM | 1,000 | 10 µM = 10,000 nM |
| mg/mL to µg/mL | 1,000 | 1 mg/mL = 1,000 µg/mL |
| kDa to Da | 1,000 | 66.5 kDa = 66,500 Da |
Frequently Asked Questions (FAQ)
To calculate protein concentration from molecular weight, use the formula: Molarity (M) = (Concentration in mg/mL × 1000) / Molecular Weight (g/mol). For example, if you have a 66.5 kDa protein at 5 mg/mL, the molar concentration is (5 × 1000) / 66,500 = 0.0000752 M or 75.2 µM. This conversion is essential because biochemical reactions occur at the molecular level, and molar units directly represent the number of protein molecules present.
mg/mL measures protein concentration by mass per volume (weight/volume), while µM (micromolar) measures by the number of moles per liter (molar concentration). The key difference is that mg/mL tells you how much protein mass is present, but µM tells you how many protein molecules are present. For comparing different proteins or calculating stoichiometry, µM is preferred because it accounts for molecular weight differences. Two proteins at the same mg/mL concentration will have different µM concentrations if they have different molecular weights.
To convert µM to mg/mL, first convert µM to molarity by dividing by 1,000,000, then use the formula: mg/mL = (Mol