MITF 抗体 (AA 1-114)
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- 抗原 See all MITF 抗体
- MITF (Microphthalmia-Associated Transcription Factor (MITF))
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抗原表位
- AA 1-114
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This MITF antibody is un-conjugated
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应用范围
- Flow Cytometry (FACS), ELISA
- 原理
- MITF Antibody
- 纯化方法
- Purified antibody
- 免疫原
- Purified recombinant fragment of human MITF (AA: 1-114) expressed in E. Coli.
- 克隆位点
- 3A2E2
- 亚型
- IgG1
- Top Product
- Discover our top product MITF Primary Antibody
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- 应用备注
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ELISA: 1/10000
FCM: 1/200 - 1/400
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified antibody in PBS with 0.05 % sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
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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
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Description: 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.
Aliases: MI, WS2, CMM8, WS2A, bHLHe32
- 分子量
- 58.8kDa
- 基因ID
- 4286
- HGNC
- 3106
- UniProt
- O75030
- 途径
- Chromatin Binding
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