| Intrument | Microplate reader (400-410 nm) |
| Assay Time | 25 min |
| Validity | 3 |
| Assay Type | Quantitative |
| Sample Type | Serum |
| Synonyms | TBA |
| Detection Principal | With S-NAD+ as hydrogen receptor, 3?-hydroxy steroid dehydrogenase catalyzed the dehydrogenation of bile acids to produce 3-ketone steroids, transforming S-NAD+ into S-NADH. Meanwhile, NADH was used as hydrogen donor. 3?-hydroxy steroid dehydrogenase catalyzed the production of bile acids from 3-ketone steroids. Through the enzyme cycle reaction, S-NADH is continuously generated, which has the maximum absorption peak at 405 nm. Measure the OD value at 405 nm and the changes of absorbance is proportional to the concentration of bile acid. |
| Reagents | Normal saline (0.9% NaCl) |
| Labware | Micropipettor, Centrifuge, Incubator, Vortex mixer |
| Size | 96T |
| Sensitivity | 2.05 ?mol/L |
| Detection Range | 2.05-120 ?mol/L |
| Recovery Rate | 97 |
| Inter CV | 3.7 |