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Triturus elisa system

Manufactured by Grifols
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Sourced in Italy

The TRITURUS ELISA system is a fully automated instrument designed for performing enzyme-linked immunosorbent assay (ELISA) testing. The system is capable of automating the essential steps of the ELISA process, including sample handling, reagent addition, incubation, and results measurement. The TRITURUS ELISA system is intended to provide efficient and consistent ELISA testing for clinical and research applications.

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Lab products found in correlation

Human saa kha0011c, by Thermo Fisher Scientific (1 mentions) Kha0011, by Thermo Fisher Scientific (1 mentions)

Close spelling variants of this product

TRITURUS automated ELISA system Triturus System Triturus

2 protocols using triturus elisa system

1

Quantifying Serum SAA Levels

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The commercially available ELISA procedure (Human SAA KHA0011C, Invitrogen, California, USA) was used to measure SAA concentration in serum, HDL2, and HDL3, specifically detecting SAA1. As per the manufacturer's instructions, analysis was performed on a TRITURUS ELISA system (Grifols, Vicopisano, Italy). Prior to analyses, samples were diluted as follows: serum, 1 : 150; HDL2, 1 : 10; and HDL3, 1 : 100. The CVs for SAA were 2.8%, 3.6%, and 5.6% (interspecific) and 8.0%, 9.5%, and 11% (intraspecific) for SAA, HDL2, and HDL3, respectively.
Griffiths K., Pazderska A., Ahmed M., McGowan A., Maxwell A.P., McEneny J., Gibney J, & McKay G.J. (2017). Type 2 Diabetes in Young Females Results in Increased Serum Amyloid A and Changes to Features of High Density Lipoproteins in Both HDL2 and HDL3. Journal of Diabetes Research, 2017, 1314864.
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2

Serum SAA and HDL Subclasses Analysis

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SAA was measured in serum, HDL2 and HDL3 by a commercially available ELISA procedure (Invitrogen, KHA0011), which detects human-SAA1 and SAA2. The analysis was performed on a Grifols TRITURUS ELISA system (Italy), as per the manufacturer's instructions, with the following modifications. Serum was diluted 1 : 150, HDL2 1 : 10 and HDL3 1 : 100. The intra- and interassay precision of this assay were both <8%. This kit did not cross-react with a wide range of other proteins, including CRP, TNF-α, and IL-6.
McEneny J., Daniels J.A., McGowan A., Gunness A., Moore K., Stevenson M., Young I.S, & Gibney J. (2015). A Cross-Sectional Study Demonstrating Increased Serum Amyloid A Related Inflammation in High-Density Lipoproteins from Subjects with Type 1 Diabetes Mellitus and How This Association Was Augmented by Poor Glycaemic Control. Journal of Diabetes Research, 2015, 351601.
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