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Home / ELISA Kit

Human Glutamine-dependent NAD (NADSYN1) ELISA Kit

SKU : BHE13703607

Nicotinamide adenine dinucleotide (NAD) is a coenzyme in metabolic redox reactions, a precursor for several cell signaling molecules, and a substrate for protein posttranslational modifications. NAD synthetase (EC 6.3.5.1) catalyzes the final step in the biosynthesis of NAD from nicotinic acid adenine dinucleotide (NaAD).

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Mfr.No.	KTE61392
Reactivity	Human
Assay Duration	Multiple steps standard sandwich ELISA assay with a working time of 3-5 hours. It depends on the experience of the operation person.
Assay Type	Sandwich (quantitative)
Description	This Human Glutamine-dependent NAD (NADSYN1) ELISA Kit employs a two-site sandwich ELISA to quantitate NADSYN1.
Alternative Names	NADSYN1; FLJ10631; FLJ36703; FLJ40627; glutamine-dependent NAD synthetase
Detection Method	Colorimetric
Kit Components	Human Glutamine-dependent NAD microplate Human Glutamine-dependent NAD standard Human Glutamine-dependent NAD detect antibody Streptavidin-HRP Standard diluent Assay buffer HRP substrate Stop solution Wash buffer Plate covers
Features	Human Glutamine-dependent NAD (NADSYN1) ELISA Kit has high sensitivity and excellent specificity for detection of Human NADSYN1. No significant cross-reactivity or interference between Human NADSYN1 and analogues was observed.
Calibration Range	Please inquire
Sample Type	Serum, Cell culture supernatants, Plasma, Other biological fluids
Limit Of Detection	Please inquire
Precautions	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.
Background	Nicotinamide adenine dinucleotide (NAD) is a coenzyme in metabolic redox reactions, a precursor for several cell signaling molecules, and a substrate for protein posttranslational modifications. NAD synthetase (EC 6.3.5.1) catalyzes the final step in the biosynthesis of NAD from nicotinic acid adenine dinucleotide (NaAD).
Notes	This Human Glutamine-dependent NAD (NADSYN1) ELISA Kit employs a two-site sandwich ELISA to quantitate NADSYN1 in samples. An antibody specific for NADSYN1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyNADSYN1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for NADSYN1 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 NADSYN1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Usage Notes	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.

Gene ID	55191

Applications	ELISA
Applications Notes	This Human Glutamine-dependent NAD (NADSYN1) ELISA Kit employs a two-site sandwich ELISA to quantitate NADSYN1 in samples. An antibody specific for NADSYN1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyNADSYN1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for NADSYN1 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 NADSYN1 bound in the initial step. The color development is stopped and the intensity of the color is measured.

Storage Instructions	The unopened kit should be stored at 2 - 8°C. After opening, please store refer to protocols.
Shipping	Gel pack with blue ice.

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SKU	Supplier No.	Size	Your price	Quantity
BHE13703607	KTE61392	48 T	$339		Add to Cart
BHE13703607	KTE61392	96 T	$589		Add to Cart
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BHE13703607	KTE61392	96 Tx50	$24569		Add to Cart

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