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The Beckman Coulter Access Insulin assay (REF 33410) is an in vitro diagnostic reagent kit intended for the quantitative determination of insulin in human serum and plasma using the Access Immunoassay family of analyzers. Built on Beckman Coulter's paramagnetic particle, chemiluminescent immunoassay technology, the assay supports laboratories investigating glucose metabolism disorders and pancreatic beta-cell function as part of a broader endocrine testing menu.
Key Features
- Paramagnetic particle, chemiluminescent immunoassay (CLIA) chemistry for sensitive insulin quantitation
- Ready-to-use reagent pack format designed for Access Immunoassay Systems
- Compatible with human serum and plasma sample types
- Calibration and quality control workflows aligned with the Access platform
- Onboard reagent handling intended to support routine laboratory throughput
- Packaged for streamlined inventory and traceability in clinical chemistry workflows
Clinical Applications
- Quantitative measurement of insulin to support investigation of carbohydrate metabolism
- Assessment of pancreatic beta-cell secretory activity in conjunction with other laboratory findings
- Support of endocrinology workups involving suspected hyperinsulinemia or hypoglycemia
- Use within laboratory testing panels alongside glucose and related analytes
- Routine endocrine immunoassay testing in hospital and reference laboratory settings
Product Information
Brand: Beckman Coulter
Product: Access Insulin Reagent
REF / UPN: 33410
Category: Laboratory - Immunoassay Reagents
Technology: Paramagnetic particle, chemiluminescent immunoassay
Analyte: Insulin
Sample Types: Human serum and plasma (refer to current IFU)
Compatible Instruments: Access Immunoassay Systems family (refer to current IFU for supported analyzers)
Tests per Kit: Not specified in the located sources
Storage Conditions: Not specified in the located sources
Shelf Life: Not specified in the located sources
Regulatory Status: Refer to the manufacturer's current labeling and Instructions for Use for intended use and regional regulatory status
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