Endothelial Lipase ELISA
- Regulatory Status
- RUO
- Kit size
- 12 x 8
- Method
- ELISA
- Incubation time
- 1 x 18h, 2 x 30 min.
- Standard range
- 31.25 - 2000 pg/mL
- Specimen / Volumes
- 100 µL serum, EDTA-plasma, cell culture supernatant
- Substrate / isotope
- TMB 450nm
Endothelial lipase (EL) is a member of the triacylglyceride lipase family, which is synthesized by vascular endothelial cells. Experiments in laboratory mice with a disrupted native EL locus as well as in transgenic mice overexpressing human EL have revealed an inverse relationship between the plasma High-Density-Lipoprotein-Cholesterol (HDL-C) level and EL expression. Also, previous studies have shown that plasma EL mass was inversely associated with HDL-C concentrations in humans. Based on these observations, EL is expected to be an attractive pharmacological target for raising HDL-C levels and preventing atherosclerosis.
This ELISA kit can measure concentration of EL in serum or plasma samples regardless of heparin administration.
Separate control set available on request
Our Product Families
Our comprehensive immunoassay portfolio includes a number of specialty diagnostic immunoassays for endocrinology, immunology and autoimmunity, as well as for diagnosis of multiple infectious diseases. We are pioneers and market leaders in saliva diagnostics, with over 40 years of experience supplying a broad portfolio of luminescence- and ELISA-based tests, including our highly acclaimed HMGB1 and MuSK-Ab ELISAs.
And as experts in laboratory automation, we can support our customers with the protocols for open ELISA platforms, such as the Freedom EVOlyzer or Thunderbolt®.
All products are only available for sale to laboratory professionals and may not be available in all countries. Availability and regulatory status may vary across regions depending on local country-specific registration. Please always read and follow the instructions for use.
All of our assays have been designed and manufactured to meet the highest global regulatory requirements and quality standards. Tecan is certified under ISO 9001:2015, ISO 13485:2016 and is audited by a notified body according to Medical Device Single Audit Program (MDSAP).
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As part of the Tecan Group, we have a leading market position in diagnostics and research, with over 40 years of experience in the development, manufacture and supply of enzyme-, radiolabel- and luminescence-based immunoassays.
Our range of high-quality immunoassays is supported by a diverse portfolio of automated solutions, making us the perfect partner for you and your customers.
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