Human N-alpha-acetyltransferase 50, NatE catalytic subunit (NAT13) ELISA Kit

NAA50 (N (Alpha) -Acetyltransferase 50, NatE Catalytic Subunit) is a Protein Coding gene. Diseases associated with NAA50 include Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant and Neuropathy, Hereditary Sensory And Autonomic, Type V. Among its related pathways are Cytochrome P450 - arranged by substrate type. GO annotations related to this gene include N-acetyltransferase activity and H4 histone acetyltransferase activity. Probable catalytic component of the NAA11-NAA15 complex which displays alpha (N-terminal) acetyltransferase activity.

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-alpha-acetyltransferase 50, NatE catalytic subunit (NAT13) ELISA Kit has high sensitivity and excellent specificity for detection of Human NAT13. No significant cross-reactivity or interference between Human NAT13 and analogues was observed.

This Human N-alpha-acetyltransferase 50, NatE catalytic subunit (NAT13) ELISA Kit employs a two-site sandwich ELISA to quantitate NAT13 in samples. An antibody specific for NAT13 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyNAT13 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for NAT13 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 NAT13 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.