LPL Monoclonal Antibody, 50ul Electronic Pipette a highly penetrant familial cancer

a highly penetrant familial cancer phenotype usually associated with inherited mutations in TP53

TFEB is activated in response to nutrient deprivation

Consisting of 237 million bases

Mutations in this gene cause ovarian dysgenesis type 1

LPL Monoclonal Antibody, 50ul Electronic Pipette a highly penetrant familial cancerLPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand bridging factor for receptor mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism.