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S100 ELISA

Catalog no.CA51311
Regulatory Status
EU: CE
Kit size
12 x 8
Method
ELISA
Incubation time
1 x 2 h, 1 x 1 h, 1 x 30 min
Standard range
50 - 3500 ng/L
Specimen / Volumes
50 µL serum
Substrate / isotope
TMB 405/620 nm
instructions for useMSDS

S100 is a 20 kDa protein belonging to the S100/calmodulin/troponin C superfamily of EF-hand calcium-binding proteins. S100 was originally isolated from human brain and considered a glial-cell specific protein (1). Today, 20 monomers of the S100 family have been identified based on structural and functional similarities (2, 3). Most of the S100 proteins exist as dimers and are expressed in a cell-specific manner. Two of the S100 monomers, designated S100A1 and S100B (4) are highly conserved between species and are found as homo- (BB) and heterodimers (A1B) in central nervous system glial cells and in certain peripheral cells eg. Schwann cells, melanocytes, adipocytes, and chondrocytes (5). S100A1B and S100BB are also present in malignant tissues, most notably in melanoma and to a lesser extent in glioma, thyroid cell carcinoma and renal cell carcinoma (2). Determination of S100B in serum has been shown to be clinically useful for prognosis and treatment monitoring of patients diagnosed with malignant melanoma (6-9). Studies also suggest that S100B may be useful in the management of patients with brain damage from eg. traumatic head injury, perinatal asphyxia, cardiac arrest, cardiac surgery and stroke

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.

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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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