Raw Materials for Life Sciences – Essential Reagents for Biotech Applications​

rBSA (Recombinant Bovine Serum Albumin) – Molecular Biology Grade

Recombinant Bovine Serum Albumin Molecular Biology Grade (rBSA Molecular Biology Grade), a non-animal albumin equivalent to the common Bovine Serum Albumin (BSA), is heterologously expressed in yeast cells. Similar to BSA, it has demonstrated efficacy in preventing enzyme adhesion to reaction tubes and pipette surfaces, while also stabilizing certain proteins during incubation, especially relevant for overnight reactions.

rBSA-recombinant-bovine-serum-albumin-molecular-biology-grade

Catalog for rBSA – Molecular Biology Grade

Cat. No.

Size

Format

MT10K-G1RBSAHA

10 mg

Liquid, glycerol-free

MT10K-S1RBSAHA

10 mg

Liquid, in glycerol

MT10K-L1RBSAHA

10 mg

Lyophilized

Applications for rBSA – Molecular Biology Grade

Documentation for rBSA – Molecular Biology Grade

Cat. No.

Technical Data Sheet

Safety Data Sheet

MT10K-G1RBSAHA

MT10K-S1RBSAHA

MT10K-L1RBSAHA

Other information about rBSA – Molecular Biology Grade

recombinant-bsa-molecular-biology-grade

Agarose gel image showing DNA digestion with different digestion enzymes after treatment including either our recombinant bovine serum albumin (rBSA) agent or commercial animal-origin BSA agent. Before and after digestion are indicated as C (control) and E (enzyme), respectively.

For more information, please refer to the Technical Data Sheet or ask our team about this product.

FAQs (Frequently Asked Questions)

Fundamentals

Recombinant bovine serum albumin (rBSA) is a bioengineered version of BSA produced through yeast-based precision fermentation rather than extracted from bovine plasma.

While animal-origin BSA depends on blood collection and purification, rBSA is manufactured in a fully controlled, animal-free system.The key differences lie in origin, consistency, and risk profile. Recombinant BSA eliminates animal-derived contaminants, reduces batch-to-batch variability, and avoids TSE/BSE-related concerns, while maintaining the functional properties expected from BSA in biotech workflows.

For molecular biology applications, this controlled and animal-free origin is especially important to minimize background interference and experimental variability.

Yes.

Levprot rBSA is designed to reproduce the native structure and biochemical functionality of bovine serum albumin. It retains the characteristic folding, binding capacity, and stabilizing behavior that make BSA essential as a carrier, protector, and buffering protein across multiple applications.

The difference is not in what the protein does, but in how it is produced and controlled. This functional equivalence is critical for molecular biology workflows that rely on predictable and reproducible protein behavior.

Yes.

Levprot recombinant BSA corresponds to the same protein entity as bovine serum albumin and therefore shares the same CAS number.

The distinction between recombinant and animal-origin BSA lies in the production method, not in the molecular identity of the protein.

Compared to ultra-pure plasma-derived BSA, recombinant BSA offers greater consistency and lower biological risk without compromising functional performance.

While ultra-pure animal-derived BSA may still present inherent variability and animal-origin risk, Levprot rBSA provides a cleaner, more reproducible alternative for demanding molecular biology applications.

Recombinant rBSA is produced in a controlled fermentation system, resulting in a highly defined and consistent protein structure.

Unlike plasma-derived BSA, recombinant rBSA does not contain bound endogenous ligands and does not oligomerize, which improves availability of functional binding sites and enhances stabilizing performance in sensitive workflows.

Plasma-derived BSA may carry residual ligands naturally present in blood, partially occupying binding sites.

Recombinant rBSA is produced in a controlled system without these endogenous ligands, meaning its binding pockets are functionally available. This can improve blocking efficiency, protein stabilization, and assay performance.

Applications

Yes.

Levprot rBSA Molecular Biology Grade is suitable for enzyme stabilization in sensitive molecular biology workflows.

Its high purity and controlled contaminant profile help preserve enzymatic activity without introducing interfering substances.

Yes.

This grade is specifically designed to meet the demands of molecular biology applications, where low background, high purity, and reproducibility are critical.

It is optimized for use in enzymatic reactions, nucleic acid handling, and other sensitive laboratory workflows.

Yes.

Levprot rBSA Molecular Biology Grade is manufactured under strict controls to ensure it is RNase-free, DNase-free, and DNA-free, making it suitable for highly sensitive molecular biology workflows.

Yes. In most molecular biology workflows, Levprot rBSA Molecular Biology Grade can be implemented using the same concentrations and protocols as plasma-derived BSA. Minor optimization may be performed depending on the application, but no structural or functional revalidation is typically required.

Storage conditions depend on the specific format (liquid or lyophilized). In general, lyophilized material should be stored refrigerated and protected from moisture, while liquid formulations should be stored at recommended temperatures to preserve stability.

Detailed storage and handling instructions are provided in the product documentation.

While plasma-derived BSA is commonly used at concentrations around 1 g/L, Levprot rBSA can often achieve comparable or improved performance at significantly lower concentrations, typically in the range of 10–50 mg/L, depending on the system and sensitivity of the assay.

This increased functional efficiency contributes to overall cost-effectiveness in many applications.

Safety & Regulatory

Yes.

Levprot rBSA Molecular Biology Grade is fully animal-free and produced using yeast-based precision fermentation.

No animal-derived raw materials are used at any stage of production.

Yes.

Since Levprot rBSA is produced through yeast-based precision fermentation without any animal-derived raw materials, it eliminates risks associated with transmissible spongiform encephalopathies (TSE/BSE) and simplifies regulatory documentation.

Yes.

Recombinant production in yeast avoids contaminants typically associated with plasma-derived materials, such as IgG, animal viruses, and other blood-borne components. The controlled fermentation and purification process supports a highly defined and reproducible contaminant profile.

Residual DNA is controlled through validated purification processes and quality testing. Batch-specific analyses are performed to ensure compliance with molecular biology requirements.

Additional information and documentation can be provided upon request to support regulatory or validation needs.

Supply

Animal-free recombinant BSA offers several advantages compared to plasma-derived BSA:

  • No animal-origin raw materials
  • No TSE/BSE-related risk or documentation
  • Improved batch-to-batch consistency
  • Scalable and secure supply through fermentation
  • Better alignment with regulatory, ethical, and sustainability requirements



These advantages make rBSA particularly well suited for molecular biology workflows requiring low background, high purity, and high reproducibility.

Yes.

Yeast-based precision fermentation enables scalable and secure production, with reliable supply independent of animal-derived supply chains, supporting long-term availability for industrial and regulated applications.

Although the unit price per gram may differ from conventional BSA, rBSA can often be used at significantly lower concentrations due to its functional efficiency.

This reduced usage, combined with improved reproducibility and lower risk, can contribute to overall cost-effectiveness in many workflows.

Yes.

Validation samples are available to support performance testing in specific workflows. Customers are encouraged to perform in-house equivalence testing to determine optimal concentrations before scaling up to production volumes.

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