Order NO. D151609
产品描述
概述
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.
应用
免疫印迹(WB),免疫组织化学(IHC),免疫荧光(IF)
属性
保存缓冲液 |
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
|
运输条件 |
2-8°C
|
靶点 Uniprot 登记号 |
O75030
|
靶点基因 ID |
4286
|
靶点全称 |
microphthalmia-associated transcription factor
|
靶点别名 |
MI; WS2; CMM8; WS2A; bHLHe32
|
靶点研究领域 |
Epigenetics and Nuclear Signaling, Immunology
|
亚型 |
Immunogen-specific rabbit IgG
|