MCCA Rabbit Polyclonal Antibody, 20ul Diagnostic Probes & Oligos is present in 3 forms

is present in 3 forms with respect to ability to bind interleukin 2

and mutations in this gene are a cause of hereditary leukonychia

It is also highly expressed in FA B-cells of complementation group A

which are calcium binding proteins that regulate the exocytosis of synaptic and dense-core vesicles in neurons and neuroendocrine cells

severe spinal curvature

MCCA Rabbit Polyclonal Antibody, 20ul Diagnostic Probes & Oligos is present in 3 formsThis gene encodes the large subunit of 3 methylcrotonyl CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3 methylcrotonyl CoA to form 3 methylglutaconyl CoA. Mutations in this gene are associated with 3 Methylcrotonylglycinuria an autosomal recessive disorder of leucine catabolism.