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MITF 抗体 (AA 1-114)
MITF
适用: 人
WB, IHC, FACS, ELISA, ICC
宿主: 小鼠
Monoclonal
8F1G5
unconjugated
MITF抗体详情
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抗原
See all MITF 抗体
MITF
(Microphthalmia-Associated Transcription Factor (MITF))
抗原表位
All epitopes for MITF 抗体
AA 1-114
适用
All reactivities for MITF 抗体
人
宿主
All hosts for MITF 抗体
小鼠
克隆类型
All clonalities for MITF 抗体
单克隆
标记
All conjugates for MITF 抗体
This MITF antibody is un-conjugated
应用范围
All applications for MITF 抗体
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS), ELISA, Immunocytochemistry (ICC)
免疫原
Purified recombinant fragment of human MITF (AA 1-114) expressed in E. Coli.
克隆位点
8F1G5
亚型
IgG1
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Discover our top product MITF Primary Antibody
Alternatives
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使用细节
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应用备注
ELISA: 1:10000, WB: 1:500 - 1:2000, IHC: , ICC: , FCM: 1:200 - 1:400
限制
仅限研究用
贮存及处理
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状态
Liquid
缓冲液
PBS with 0.05 % sodium azide
储存条件
4 °C,-20 °C
储存方法
4°C, -20°C for long term storage
MITF目标详情
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抗原
MITF
(Microphthalmia-Associated Transcription Factor (MITF))
别名
MITF (MITF 产品 )
别名
MITF antibody, ws2a antibody, mitfa antibody, MITF-A antibody, LOC100313655 antibody, mitfb antibody, CMM8 antibody, MI antibody, WS2 antibody, WS2A antibody, bHLHe32 antibody, BCC2 antibody, Bhlhe32 antibody, Gsfbcc2 antibody, Vitiligo antibody, Wh antibody, bw antibody, mi antibody, vit antibody, MITF-H antibody, MITF-M antibody, CMI9 antibody, melanogenesis associated transcription factor antibody, microphthalmia-associated transcription factor antibody, microphthalmia-associated transcription factor S homeolog antibody, Microphthalmia antibody, MITF antibody, mitf antibody, LOC100313655 antibody, mitf.S antibody, LOC100534525 antibody, MICROP antibody, Mitf antibody
背景
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.,
分子量
66.2kDa
HGNC
2099
途径
Chromatin Binding
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