MITF Polyclonal Antibody, 50ul Glassware Sets such as the placenta and

such as the placenta and testis

ketoglutarate

A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD)

This gene is a member of the ecto-nucleotide pyrophosphatase/phosphodiesterase (ENPP) family

Alternate use of an in-frame upstream non-AUG (CUG) translation initiation codon| and a downstream AUG codon| results in two isoforms

MITF Polyclonal Antibody, 50ul Glassware Sets such as the placenta andMITF encodes microphthalmia associated transcription factor that contains both basic helix loop helix and leucine zipper structural features. It regulates the differentiation and development of melanocytes retinal pigment epithelium and is also responsible for pigment cell specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz