Human Transmembrane prolyl 4-hydroxylase (P4HTM) ELISA Kit

Catalog Number: BYT-ORB1291359
Article Name: Human Transmembrane prolyl 4-hydroxylase (P4HTM) ELISA Kit
Biozol Catalog Number: BYT-ORB1291359
Supplier Catalog Number: orb1291359
Alternative Catalog Number: BYT-ORB1291359-48, BYT-ORB1291359-96
Manufacturer: Biorbyt
Category: Kits/Assays
Application: ELISA
Species Reactivity: Human
Alternative Names: EGLN4, FLJ20262, HIF prolyl hydroxylase PH4, HIF-PH4, HIF-prolyl hydroxylase 4, HIFPH4, HPH-4, Hypoxia inducible factor prolyl 4 hydroxylase, Hypoxia inducible factor prolyl hydroxylase, Hypoxia-inducible factor prolyl hydroxylase 4, P4H TM, P4H with transmembrane domain, P4H-TM, P4htm, P4HTM_HUMAN, PH 4, PH4, PHD4, Proline 4 hydroxylase, Prolyl 4 hydroxylase transmembrane (endoplasmic reticulum), Prolyl hydroxlase domain containing 4, Transmembrane prolyl 4-hydroxylase,
Human P4HTM (Transmembrane prolyl 4-hydroxylase) ELISA Kit
Concentration: 1000 pg/mL
Range: 15.63-1000 pg/mL
Sensitivity: 5.5 pg/mL
UniProt: Q9NXG6
Samples: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Application Notes: Application Notes: standard: 1000 pg/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human P4HTM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human P4HTM. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human P4HTM, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm 10nm. The concentration of Human P4HTM in the samples is then determined by comparing the OD of the samples to the standard curve