SP5 Polyclonal Antibody, 50ul[BT-AP14398] Multiplex Immunoassays Mutations in this gene cause

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

AMP-N-alanine methyl ester

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

the enzyme encoded by the INDOL1 gene metabolizes tryptophan in the kynurenine pathway (Ball et al

a rare autosomal recessive lipid storage disease

SP5 Polyclonal Antibody, 50ul[BT-AP14398] Multiplex Immunoassays Mutations in this gene causeBinds 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.,