Separate IgG from BSA

Separation strategy for IgG (150 kDa) from BSA (66 kDa) using Affinity Chromatography.

Recommended technique

Affinity Chromatography Best Match

Separation handle: Antibody capture via Protein A.

Scope: Biospecific. CAPEX range: $200k-$2M.

Property comparison

PropertyIgGBSA
Molecular weight150000 Da66500 Da
Solubility (water)150 g/L400 g/L
Charge5-18
Isoelectric point8.54.7
pKa8.54.7
Density1.38 g/cm³1.37 g/cm³
Diffusion coefficient4.00e-07 cm²/s5.90e-07 cm²/s
Log P

Process design walkthrough

1

Define your feed stream

Set IgG and BSA as components with their concentrations and physical properties. Use the molecule database to auto-populate properties.

2

Drop in Affinity Chromatography

Connect the feed inlet, configure operating parameters (MWCO, pH, eluent, residence time as relevant), and connect the two outlets to product and waste streams.

3

Run the simulation

untangle.bio calculates outlet concentrations using mass balance and the separation function for this technique. Iterate on parameters to optimise yield vs purity.

4

Add polishing if needed

If the single step doesn't meet your purity spec, add a second separation with a complementary handle (e.g., size after charge, hydrophobicity after size).

Frequently Asked Questions

Why is Affinity Chromatography the right choice for this pair?

Affinity Chromatography exploits antibody capture via protein a as the separation handle. The property gap between IgG and BSA on this axis is large enough to give a clean separation in a single step at industrially relevant flow rates.

What yield and purity can I expect?

Typical single-step recovery is 85-99% depending on operating conditions. Purity from a single affinity chromatography step is in the 90-99% range; polishing steps push above 99.5%.

What does this step cost to operate?

Capital cost for Affinity Chromatography at biotech scale is in the $200k-$2M range. Operating cost depends on scale, feed concentration, and product value. See the technique page for details.

How do I design this in untangle.bio?

Drop a affinity chromatography unit operation into the flowsheet, connect the feed stream containing both IgG and BSA, and the simulator will calculate mass balance and expected outlet concentrations using the molecule database properties.

Design this separation in untangle.bio

Build a flowsheet, simulate yield and purity, and estimate CAPEX for separating IgG from BSA.

Open untangle.bio

Related pages

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