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- Tel: 858.663.9055
- Email: info@nsjbio.com
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This gene encodes a 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 syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.
Titration of the MITF antibody may be required due to differences in protocols and secondary/substrate sensitivity.
A portion of amino acids 1-28 from the human protein was used as the immunogen for this MITF antibody.
Aliquot the MITF antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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