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)

such as the placenta and testis

The encoded protein is an anti-apoptotic factor that acts as an inhibitor of caspases 3 and 7 in the cytoplasm

This regulation is thought to involve the inhibition of neurotransmitter release by reducing calcium ion currents and increasing potassium ion conductance

The encoded protein removes glucuronide from mycophenolic acid acyl-glucuronide

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