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MITF 抗体 (AA 1-114)

MITF 适用: 人 FACS, ELISA 宿主: 小鼠 Monoclonal 3A2E2 unconjugated
产品编号 ABIN5542530
发货至: 中国
  • 抗原 See all MITF 抗体
    MITF (Microphthalmia-Associated Transcription Factor (MITF))
    抗原表位
    • 17
    • 15
    • 13
    • 9
    • 8
    • 5
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-114
    适用
    • 100
    • 50
    • 25
    • 17
    • 5
    • 5
    • 5
    • 5
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    宿主
    • 76
    • 39
    • 1
    小鼠
    克隆类型
    • 67
    • 49
    单克隆
    标记
    • 63
    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MITF antibody is un-conjugated
    应用范围
    • 68
    • 48
    • 41
    • 35
    • 34
    • 17
    • 13
    • 7
    • 7
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    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
  • 应用备注

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    限制
    仅限研究用
  • 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.
  • 抗原
    MITF (Microphthalmia-Associated Transcription Factor (MITF))
    别名
    MITF (MITF 产品)
    背景

    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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