LPD lipase Polyclonal Antibody

    • Catalog No.:YT2586
    • Applications:WB;IHC;IF;ELISA
    • Reactivity:Human;Rat;Mouse;
      • Target:
      • LPD lipase
      • Gene Name:
      • LIPI
      • Protein Name:
      • Lipase member I
      • Human Swiss Prot No:
      • Q6XZB0
      • Immunogen:
      • The antiserum was produced against synthesized peptide derived from human LIPI. AA range:289-338
      • Specificity:
      • LPD lipase Polyclonal Antibody detects endogenous levels of LPD lipase protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • LIPI;LPDL;PRED5;Lipase member I;LIPI;Cancer/testis antigen 17;CT17;LPD lipase;Membrane-associated phosphatidic acid-selective phospholipase A1-beta;mPA-PLA1 beta
      • Observed Band(KD):
      • 53kD
      • Background:
      • The protein encoded by this gene is a phospholipase that hydrolyzes phosphatidic acid to produce lysophosphatidic acid. Defects in this gene are a cause of susceptibility to familial hypertrigliceridemia. This gene is also expressed at high levels in Ewing family tumor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014],
      • Function:
      • disease:Defects in LIPI may be a cause of susceptibility to familial hypertrigliceridemia [MIM:145750]. Familial hypertriglyceridemia is a common inherited disorder in which the concentration of very low density lipoprotein (VLDL) is elevated in the plasma. This leads to increased risk of heart disease, obesity, and pancreatitis.,enzyme regulation:Inhibited by sodium vanadate.,function:Hydrolyzes specifically phosphatidic acid (PA) to produce lysophosphatidic acid (LPA).,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the AB hydrolase superfamily. Lipase family.,subcellular location:May associate with lipid draft.,subunit:Interacts with heparin with a high affinity.,tissue specificity:Expressed in testis. Expressed exclusively at the connecting piece of the sperm.,
      • Subcellular Location:
      • [Isoform 1]: Cell membrane . Secreted . May associate with lipid draft. .; [Isoform 2]: Cell membrane . Secreted . May associate with lipid draft. .
      • Expression:
      • Expressed in testis. Expressed exclusively at the connecting piece of the sperm.
      • Products Images
      • Western Blot analysis of various cells using LPD lipase Polyclonal Antibody
      • Western blot analysis of lysates from COLO cells, using LIPI Antibody. The lane on the right is blocked with the synthesized peptide.
      • Western blot analysis of the lysates from HepG2 cells using LIPI antibody.
      • Immunohistochemical analysis of paraffin-embedded human tonsil. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).