SP5 Polyclonal Antibody, 50ul[BT-AP14398] Multiplex Immunoassays AMP-N-alanine methyl ester

AMP-N-alanine methyl ester

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

Alternative splicing of this gene results in two transcript variants

a rare autosomal recessive lipid storage disease

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

SP5 Polyclonal Antibody, 50ul[BT-AP14398] Multiplex Immunoassays AMP-N-alanine methyl esterBinds 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.,