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Lipoprotein Lp(a) ELISA

Catalog no.30124635
Regulatory Status
EU: CE
Kit size
12 x 8
Method
ELISA
Incubation time
1 x 1h, 1 x 15min
Specimen / Volumes
25 µL serum, plasma
Substrate / isotope
TMB 450 nm
instructions for use

Lp(a) ELISA provides a method for the quantitative determination of human Lp(a) in serum or plasma. Apolipoprotein(a), Apo(a), is a glycoprotein linked by disulphide bridges to apolipoprotein B in the Lp(a) particle. Apo(a) is formed by three different structural domains. One of the domains, called kringle 4, type 2, is present in multiple copies, the number of which varies and is genetically determined, giving rise to different sizes of Apo(a). Depending on the method used, six to 23 different isoforms of Apo(a) ranging from about 300 to 900 kD have been identified. Most individuals have two Apo(a) isoforms, although in some subjects no Apo(a) band can be detected when analyzed in SDS-gel electrophoresis followed by immunoblotting. Recently, much interest has been focused on Lp(a) since there is a lot of evidence that circulating levels represents an independent risk factor for coronary vascular disease. The Lp(a) level has been found to be an inherited risk factor for ischaemic heart disease. High Lp(a) levels have been demonstrated in familial hypercholesterolemia and its measurement may be clinically useful for risk prediction in these patients. Distributed by IBL International.

For concrete data please consult the Instruction for Use in the download box on the top right side.

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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.

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