PIGP (phosphatidylinositol glycan anchor biosynthesis class P) is a protein coding gene.
Diseases associated with PIGP include epileptic encephalopathy, early infantile, 55 and epileptic encephalopathy, early infantile, 15.
Among its related pathways are glycosylphosphatidylinositol (GPI)-anchor biosynthesis and metabolism.
PIGP encodes an enzyme involved in the first step of glycosylphosphatidylinositol (GPI)-anchor biosynthesis.
The GPI-anchor is a glycolipid found on many blood cells that serves to anchor proteins to the cell surface.
The encoded protein is a component of the GPI-N-acetylglucosaminyltransferase complex that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc to phosphatidylinositol (PI).
PIGP is located in the Down Syndrome critical region on chromosome 21 and is a candidate for the pathogenesis of Down syndrome.
PIGP has multiple pseudogenes and is a member of the phosphatidylinositol glycan anchor biosynthesis gene family.
Alternatively spliced transcript variants encoding different isoforms have been described.
Applications:Suitable for use in Western Blot and ELISA.
Other applications not tested.
Recommended Dilution:Western Blot:1:500-1:2000ELISA: 1:5000-1:20,000Optimal dilutions to be determined by the researcher.
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months after receipt.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：100ul
Host：rabbit
Source Antibody：human
Grade：Affinity Purified
Purity：Purified by immunoaffinity chromatography.
Form：Supplied as a liquid in PBS, pH 7.4, 0.02% sodium azide, 50% glycerol.
Specificity：Recognizes endogenous levels of human PIGP. Species Crossreactivity: mouse
Isotype：IgG
Calc Applications Abbrev：E WB
Calc Crossreactivity：Hu Mo
Immunogen：Synthetic peptide corresponding to aa70-150 from human PIGP.
