MITF Polyclonal Antibody, 100ul Inoculating Loops/Needles Polymorphisms in this gene have

Polymorphisms in this gene have been associated with Alzheimer's disease

Carrier of the growing fatty acid chain in fatty acid biosynthesis in mitochondria

The protein encoded by this gene is similar to Ke6 and is a member of the short-chain dehydrogenase superfamily

a transcription factor which regulates the expression of several hepatic genes

Defects in this gene cause autosomal dominant spinocerebellar ataxia 12 (SCA12)

MITF Polyclonal Antibody, 100ul Inoculating Loops/Needles Polymorphisms in this gene haveMITF 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