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Control products and reagents designed for clinical testing procedures. Ideal for use in performing, calibrating, monitoring, and ensuring the accuracy of diagnostic tests such as immunoassays.
Linearity FD Urine Chemistry Panel 1 for Abbott Systems is intended to simulate human patient urine chemistry samples for purpose of determining linearity, calibration verification and verification of reportable range for Phosphorous, Urea Nitrogen and Uric Acid.
MDx-Chex for BC-GP and MDx-Chex for BC-GN are controls designed to evaluate the entire analytical process of the Luminex VERIGENE™ BC-GP and BC-GN Panels for sepsis. With MDx-Chex for BC-GP and MDx-Chex for BC-GN, you can track lot-to-lot performance of the BC-GP and BC-GN assays and reduce the occurrence of incorrect results due to instrument or assay failures.
The Linearity FLQ Vitamin D is intended to simulate human patient samples for use in determining linearity, calibration verification, and the verification of reportable range for Vitamin D.
MDx-Chex for BC-GP and MDx-Chex for BC-GN are controls designed to evaluate the entire analytical process of the Luminex VERIGENE™ BC-GP and BC-GN Panels for sepsis. With MDx-Chex for BC-GP and MDx-Chex for BC-GN, you can track lot-to-lot performance of the BC-GP and BC-GN assays and reduce the occurrence of incorrect results due to instrument or assay failures.
The ASI CRP Slide Test is a convenient and specific slide agglutination assay for the qualitative and semiquantitative detection of C-Reactive Protein (CRP) in human serum.
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
NATtrol™ Tropical Fever Verification Panel (NATTFP-BIO) contains purified, intact bacteria and viruses that have been chemically modified to render them non-infectious and refrigerator stable. The panel members are supplied in a proprietary matrix.
CD-Chex CD34 is a three-level process control for enumerating CD34 positive cells by flow cytometry. It requires no dilution and provides reference values similar to levels found in bone marrow, cord blood and mobilized patient samples.
The OraQuick™ HCV Visual Reference Panel is intended to assist new operators in becoming proficient at reading specimens with antibody levels near the limit of detection of the device.
Designed to evaluate the performance of nucleic acid tests for determination of the presence of EBV DNA, can also be used for validation of clinical assays, development of diagnostic tests and training of laboratory personnel
HCV Testing anytime, anywhere made easy. The OraQuick™ HCV test is the only point-of-care Hepatitis C test on the market today, detecting HCV antibodies in fingerstick and venipuncture whole blood. Yielding accurate results in as little as 20 minutes.