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MITF
Melanocyte inducing transcription factorbHLHe32, MI, WS2, WS2A
The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is 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. [provided by RefSeq, Aug 2017]
Top validated antibodies |
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| Invitrogen Antibodies |  MA5-32554 |
2 references | Monoclonal |
WB
ICC
FC
OA
|
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| Proteintech Group | 13092-1-AP |
12 references | Polyclonal |
WB
EL
IP
FC
|
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| NSJ Bioreagents | V2712 |
9 references | Monoclonal |
WB
ICC
IHC
FC
OA
|
|
| OriGene | AM05308PU-N |
1 references | Monoclonal |
WB
IP
IHC
IEM
|
|
| GeneTex | GTX12039 |
1 references | Monoclonal |
WB
IP
IHC
GS
|
|
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