ARG83788

arigoQIK® Mammal Neurofilament NF-L ELISA Development Kit

arigoQIK® Mammal Neurofilament NF-L ELISA Development Kit for ELISA and Mammal

Overview

Product Description ARG83788 arigoQIK® Mammal Neurofilament NF-L ELISA Development Kit, includes Capture antibody, Detection antibody, Standard, and HRP-Streptavidin Solution.
This ELISA Development Kit is designed for the development of sandwich ELISA to measure Mammal Neurofilament NF-L in Serum, plasma and cell culture supernatants.

For other reagents required for arigoQIK® ELISA Development Kit, please refer ARG83524 Integral Reagent Kit (ELISA Development Kit)

More aboutarigoQIK® :
● Optimized capture and detection antibody pairs
● Reduced incubation time and wash cycles
● 2-hour quicker than conventional ELISA process
● 5- and 15-plate packages available
Tested Reactivity Mamm
Tested Application ELISA
Target Name Neurofilament NF-L
Conjugation HRP
Conjugation Note Substrate: TMB and read at 450 nm.
Sensitivity 8 pg/mL
Sample Type Serum, plasma and cell culture supernatants.
Standard Range 15.63-1000 pg/mL
Sample Volume 50 μL
Precision Intra-Assay CV: < 10%
Inter-Assay CV: < 10%
Alternate Names Neurofilament triplet L protein; 68 kDa neurofilament protein; CMT1F; NF68; NFL; CMT2E; Neurofilament light polypeptide; NF-L; PPP1R110

Properties

Storage Instruction Store components at 4°C or -20°C. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Gene Symbol NEFL
Gene Full Name neurofilament, light polypeptide
Background Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the light chain neurofilament protein. Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E), disorders of the peripheral nervous system that are characterized by distinct neuropathies. A pseudogene has been identified on chromosome Y. [provided by RefSeq, Oct 2008]
Function Neurofilaments usually contain three intermediate filament proteins: L, M, and H which are involved in the maintenance of neuronal caliber. [UniProt]
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PTM O-glycosylated.

Phosphorylated in the head and rod regions by the PKC kinase PKN1, leading to the inhibition of polymerization.

Ubiquitinated in the presence of TRIM2 and UBE2D1. [UniProt]
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