MITF Polyclonal Antibody, 50ul Glassware Sets A mutation in this gene

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

ketoglutarate

Two transcript variants encoding different isoforms and one non-coding transcript have been found for this gene

The encoded protein removes glucuronide from mycophenolic acid acyl-glucuronide

The encoded protein is highly basic| contains a PAZ domain and a PIWI domain| and may play a role in short-interfering-RNA-mediated gene silencing

MITF Polyclonal Antibody, 50ul Glassware Sets A mutation in this geneMITF 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