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HOME > Cell Biology > Cell signaling
NADH Assay Kit
   
ÄÚ    µå : 15261
´Ü     À§ : 400 assay
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  NADH Assay
Amplite¢â Fluorimetric NADH Assay Kit *Red Fluorescence*



Nicotinamide adenine dinucleotide (NAD+) and nicotinamide adenine dinucleotide phosphate (NADP+) are two important cofactors found in cells. NADH is the reduced form of NAD+, and NAD+ is the oxidized form of NADH. It forms NADP with the addition of a phosphate group to the 2' position of the adenyl nucleotide through an ester linkage. NADP is used in anabolic biological reactions, such as fatty acid and nucleic acid synthesis, which require NADPH as a reducing agent. In chloroplasts, NADP is an oxidizing agent important in the preliminary reactions of photosynthesis. The NADPH produced by photosynthesis is then used as reducing power for the biosynthetic reactions in the Calvin cycle of photosynthesis. The traditional NAD/NADH and NADP/NADPH assays are done by monitoring of NADH or NADPH absorption at 340 nm. This method suffers low sensitivity and high interference since the assay is done in the UV range that requires expensive quartz microplate. This Amplite¢â NADH Assay Kit provides a convenient method for sensitive detection of NADH. The enzymes in the system specifically recognize NADH in an enzyme cycling reaction. The enzyme cycling reaction significantly increases detection sensitivity.


Key Features

Broad Application: Can be used for quantifying NADH in solutions, in cell extracts.
Sensitive: The kit detect as low as 10 nanomoles of NADH in solution.
Continuous: Easily adapted to automation with no separation required.
Convenient: Formulated to have minimal hands-on time. No wash is required.
Non-Radioactive: No special requirements for waste treatment.

Kit Components

Component A: NADH recycling enzyme mixture 2 bottles (lyophilized powder)
Component B: NADH assay buffer 1 bottle (20 ml)
Component C: NADH standard 1 vial (142 ¥ìg)

Brief Summary

¡æ Prepare NADH reaction mixture (50 ¥ìL)
¡æ Add NADH standards or test samples (50 ¥ìL)
¡æ Incubate at room temperature for 15 min-2hr
¡æ Read fluorescence at Ex 540 nm/Em 590 nm

References

1. Ziegenhorn J, Senn M, Bucher T. (1976) Molar absorptivities of beta-NADH and beta-NADPH. Clin Chem, 22, 151.
2. Ikegami T, Kameyama E, Yamamoto SY, Minami Y, Yubisui T. (2007) Structure and Properties of the Recombinant     NADH-Cytochrome b(5) Reductase of Physarum polycephalum. Biosci Biotechnol Biochem.
3. Kimura N, Fukuwatari T, Sasaki R, Shibata K. (2006) Comparison of metabolic fates of nicotinamide, NAD+ and     NADH administered orally and intraperitoneally; characterization of oral NADH. J Nutr Sci Vitaminol (Tokyo), 52, 142.
4. O'Donnell JM, Kudej RK, LaNoue KF, Vatner SF, Lewandowski ED. (2004) Limited transfer of cytosolic NADH into     mitochondria at high cardiac workload. Am J Physiol Heart Circ Physiol, 286, H2237.
   
 
  15261

Product Code

Unit

Price

Availability

15261

400 assay