Human N-acetylaspartate synthetase (NAT8L) ELISA Kit

NAT8L encodes a single-pass membrane protein, which contains a conserved sequence of the GCN5 or NAT superfamily of N-acetyltransferases and is a member of the N-acyltransferase (NAT) superfamily. N-acetylaspartate synthetase is a neuron-specific protein and is the N-acetylaspartate (NAA) biosynthetic enzyme, catalyzing the NAA synthesis from L-aspartate and acetyl-CoA. NAA is a major storage and transport form of acetyl coenzyme A specific to the nervous system. NAT8L mutation results in primary NAA deficiency (hypoacetylaspartia) .

The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Human N-acetylaspartate synthetase (NAT8L) ELISA Kit has high sensitivity and excellent specificity for detection of Human NAT8L. No significant cross-reactivity or interference between Human NAT8L and analogues was observed.

This Human N-acetylaspartate synthetase (NAT8L) ELISA Kit employs a two-site sandwich ELISA to quantitate NAT8L in samples. An antibody specific for NAT8L has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyNAT8L present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for NAT8L is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of NAT8L bound in the initial step. The color development is stopped and the intensity of the color is measured.

• Do not mix components from different kit lots or use reagents beyond the kit expiration date.• Allow all reagents to warm to room temperature for at least 30 minutes before opening.• Pre-rinse the pipet tip with reagent, use fresh pipet tips for each sample, standard and reagent to avoid contamination.• Unused wells must be kept desiccated at 4 °C in the sealed bag provided.• Mix Thoroughly is very important for the result. It is recommended using low frequency oscillator or slight hand shaking every 10 minutes.• It is recommended that all samples and standards be assayed in duplicate or triplicate.