ELISA N-methyl-D-aspartic Acid IgG anti-(NMDA-Ab-IgG)

Reactivity: (Homo sapiens) UniProt:N/A Abbreviation:NMDA-Ab-IgG Alternative Names:N/A Application:ELISA Range:0.312-20 ng/mL Sensitivity:0.115 ng/mL Intra-AssayCV:?4.7% Inter-AssayCV:?6.6% Recovery:0.88 Sample Type:Serum, Plasma, Other biological fluids Detection Method:Competitive ELISA Analysis Method??:Qualitative Test principle:This assay employs the competitive enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to NMDA-Ab-IgG. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjµgated NMDA-Ab-IgG and incubated. The competitive inhibition reaction is launched between with HRP labeled NMDA-Ab-IgG and unlabeled NMDA-Ab-IgG with the antibody. A substrate solution is added to the wells and the color develops in opposite to the amount of NMDA-Ab-IgG in the sample. The color development is stopped and the intensity of the color is measured. Product Overview:Glutamate [NMDA] receptor subunit zeta-1 is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with mµLtiple subunits arranged to form a ligand-gated ion channel. These subunits play a key role in the plasticity of synapses, which is believed to underlie memory and learning. The gene consists of 21 exons and is alternatively spliced, producing transcript variants differing in the C-terminus. Althoµgh the sequence of exon 5 is identical in and rat, the alternative exon 5 splicing in rat has yet to be demonstrated in Cell-specific factors are thoµght to control expression of different isoforms, possibly contributing to the functional diversity of the subunits. Stability:The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calcµLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).