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Comprehensive QC testing programs to ensure reagent specifications and quality

Testing Services at Boston BioProducts

Explore customizable study designs and configurable QC panels.

Reagent Stability Studies

Reagent Stability Studies

Determine your reagent’s shelf-life or explore a safe extension. Choose real-time or accelerated studies to help assess product shelf life.

Quality Control Testing

Quality Control Testing

Verify product characteristics and screen for contamination before release.

QC Test Builder

QC Test Builder

Design and build your own QC testing panel. Select from a menu of 16 QC tests, send us your samples, and receive testing results.

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Featured Products
Phosphate Buffered Saline, PBS (pH 7.4, Sterile-Filtered)
Phosphate Buffered Saline (PBS) is a versatile buffer solution widely used in biological research due to its isotonic and non-toxic nature to cells. With a pH range of 7.0 to 7.4, PBS mimics the osmolarity and ion concentrations of the human body, making it ideal for a variety of applications including protein purification, as wash buffer in Western blot and immunoassays, sample dilution, and as a transport medium for tissue samples as well as RNA viruses.
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Tris-Glycine-SDS Running Buffer (10X)
The Tris-Glycine-SDS Running Buffer is the most commonly used buffer for the separation/resolution of proteins in their denatured state during SDS-PAGE. It serves as both the anode and cathode buffer during gel electrophoresis and helps to regulate the pH of the electrophoresis system. When diluted to 1X, this buffer regulates pH levels at a pH of about 8.6, which provides reproducible separation of a wide range of proteins into well-resolved bands, depending upon the gel percentage used.
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Transfer Buffer (10X, Electro Blotting)
The 10X Transfer Buffer-Electro Blotting is the most common buffer used in the wet transfer system for the electro transfer of proteins. The buffer facilitates protein transfer from SDS-PAGE gels to nitrocellulose or PVDF membranes. Ready-to-use solution once diluted to 1X working concentration; Methanol can be added to the final concentration of 10-20% (v/v) as per user protocol. This buffer prevents the gel from swelling during transfer and enhances efficiency of low abundancy proteins and protein binding to nitrocellulose membrane. This buffer is also used as a running buffer for native protein gel electrophoresis.
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