ARI3B Rabbit Polyclonal Antibody, 20ul Measuring Instruments Severe mutations that cause LPL

Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia

including the rodent NKRP1 family of glycoproteins

subunit:Part of a complex containing FRS2

This protein also plays a role in early embryonic development of the intestinal tract

ARI3B Rabbit Polyclonal Antibody, 20ul Measuring Instruments Severe mutations that cause LPLThis gene encodes a member of the ARID (AT rich interaction domain) family of DNA binding proteins. The encoded protein is homologous with two proteins that bind to the retinoblastoma gene product, and also with the mouse Bright and Drosophila dead ringer proteins. A pseudogene on chromosome 1p31 exists for this gene. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional