Species Reactivity : Human (Homo sapiens)
UniProt : Q8WWY8
Abbreviation : LIPH
Alternative Names : AH; LPDLR; PLA1B; mPA-PLA1; lipase H|mPA-PLA1 alpha|membrane-bound phosphatidic acid-selective phospholipase A1
Application : ELISA
Range : 1.56-100 ng/mL
Sensitivity : 0.68 ng/mL
Intra-AssayCV : ?4.6%
Inter-AssayCV : ?8.2%
Recovery : 0.89
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate LIPH in samples. An antibody specific for LIPH has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyLIPH present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for LIPH is added to the wells. After washing, Streptavidin conj µgated 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 LIPH bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Lipase member H is a membrane-bound member of the mammalian triglyceride lipase family. It catalyzes the production of 2-acyl lysophosphatidic acid (LPA), which is a lipid mediator with diverse biological properties that include platelet aggregation, smooth muscle contraction, and stim µLation of cell proliferation and motility.Present in intestine (at protein level). Expressed in colon, prostate, kidney, pancreas, ovary, testis, intestine, lung and pancreas. Expressed at lower level in brain, spleen and heart. In hair, it is prominently expressed in hair follicles, including the stem cell-rich b µLge region.Defects in LIPH are the cause of alopecia universalis congenita Mari type (AUCM). AUCM is a recessive autosomal form of alopecia that is common in the Mari pop µLation, a large aboriginal Finno- µgric pop µLation in the Volga-Ural region of Russia.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).