NCF1C Rabbit Polyclonal Antibody, 50ul Bottle-Top Dispenser AADCD deficiency is an inborn

AADCD deficiency is an inborn error in neurotransmitter metabolism that leads to combined serotonin and catecholamine deficiency

see UNC5C (MIM 603610)

The cytokine encoded by this gene displays chemotactic activity for normal peripheral blood eosinophils and basophils

FOXE1 functions as a thyroid transcription factor which likely plays a crucial role in thyroid morphogenesis

NCF1C Rabbit Polyclonal Antibody, 50ul Bottle-Top Dispenser AADCD deficiency is an inbornThe neutrophil cytosolic factor 1 (NCF1) gene encodes the 47 kDa cytosolic subunit of neutrophil NADPH oxidase which produces superoxide anion. The NCF1 gene is located in close proximity to two highly similar multi exon pseudogenes at chromosome 7q11. 23 corresponding to this gene record and GeneID: 654816. The two pseudogenes contain a dinucleotide deletion (delta GT) in exon 2 that results in a frameshift and truncation of the open reading frame