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NF-light (Neurofilament-light) RUO ELISA

Catalog no.30112458
Regulatory Status
RUO
Kit size
12 x 8
Method
ELISA
Incubation time
1 x 1h, 1 x 45min, 1 x 30min, 1 x 15min
Standard range
100 - 10000 ng/L
Specimen / Volumes
50 µL CSF
Substrate / isotope
TMB 450nm
instructions for useMSDS

The NF-Light™ (Neurofilament light) ELISA allows fast (3 hours) quantification of the neurofilament light chain. The assessment requires as little as 50 µL of CSF. Neurofilament light is found to be elevated in neurodegenerative disorders that are associated with the destruction of white matter (substantia alba).

The assay was developed by UmanDiagnostics, a company focusing on the development of immunochemical tools for research of neurological and traumatic injuries. The NF-Light™ (Neurofilament light) ELISA is exclusively distributed by IBL International.

Neurofilaments are the backbone of the neuronal cytoskeleton. Inside the axons, phosphorylation and dephosphorylation of the neurofilaments regulate, respectively, the expansion and contraction of the microtubules. The neurofilament light (NF-light) chain is the stoichiometrically most common form compared to other isoforms, such as medium and heavy chains. It is rapidly released after axonal destruction and remains highly stable (at least for 8 days, even at room temperature).

Distributed by TECAN, 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.

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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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