Clinical Chemistry Controls
Revvity Health Sciences Inc HTRF Human & Mouse Phospho-Rb (Ser780) Detection Kit, 50,000 Assay Points
HTRF Human & Mouse Phospho-Rb (Ser780) Detection Kit, 50,000 Assay Points
Genscript Corporation SAA Antigen
Serum Amyloid A (SAA) is an acute-phase protein The concentration of SAA in blood increases rapidly when tissue damage or inflammation occurs It is considered as an early biomarker for the diagnosis of many inflammatory diseases SAA can also be used as an important indicator of infection
Randox Fructosamine Control Level 1, Lyophilised, Human-based serum, 3 x 1 ml, Assayed, Control Level 1
The Randox Acusera Fructosamine Control Level 1 (FR2994) is designed for in vitro diagnostic use, specifically to monitor the accuracy and precision of fructosamine assays on clinical chemistry systems. It features enhanced stability and minimizes waste, with a working stability lasting to its expiry at 2°C to 8°C, and a reconstituted stability of 28 days under the same conditions. It is ideal for facilities that require reliable quality control for diabetes monitoring.
- Engineered for in vitro diagnostic use
- Monitors accuracy of fructosamine assays
- Enhanced stability to expiry at 2°C to 8°C
- 28-day reconstituted stability at 2°C to 8°C
- Designed for quality control in clinical settings
- Matrix: Human based serum
- Volume: 3 x 1 ml
- Assayed values for reliable reporting
- Suitable for diabetes monitoring applications
ABclonal Technology Ferritin Heavy Chain Rabbit pAb
This gene encodes the heavy subunit of ferritin, the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined.
ABclonal Technology Apolipoprotein CI Rabbit mAb
This gene encodes a member of the apolipoprotein C1 family. This gene is expressed primarily in the liver, and it is activated when monocytes differentiate into macrophages. The encoded protein plays a central role in high density lipoprotein (HDL) and very low density lipoprotein (VLDL) metabolism. This protein has also been shown to inhibit cholesteryl ester transfer protein in plasma. A pseudogene of this gene is located 4 kb downstream in the same orientation, on the same chromosome. This gene is mapped to chromosome 19, where it resides within a apolipoprotein gene cluster. Alternative splicing and the use of alternative promoters results in multiple transcript variants.