SP5 Polyclonal Antibody, 50ul[BT-AP14398] Multiplex Immunoassays a rare autosomal recessive lipid

a rare autosomal recessive lipid storage disease

Defects in this gene are the cause of hypoparathyroidism with sensorineural deafness and renal dysplasia

Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3

This Tribbles member induces apoptosis of cells mainly of the hematopoietic origin

an angiostatin binding protein that regulates endothelial cell migration and capillary formation

SP5 Polyclonal Antibody, 50ul[BT-AP14398] Multiplex Immunoassays a rare autosomal recessive lipidBinds to GC boxes promoters elements. Probable transcriptional activator that has a role in the coordination of changes in transcription required to generate pattern in the developing embryo.,Belongs to the Sp1 C2H2 type zinc finger protein family.,Contains 3 C2H2 type zinc fingers.,