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MNX1 抗体

MNX1 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2457924
发货至: 中国
  • 抗原 See all MNX1 抗体
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    适用
    • 58
    • 31
    • 30
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 64
    克隆类型
    • 63
    • 1
    多克隆
    标记
    • 25
    • 6
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This MNX1 antibody is un-conjugated
    应用范围
    • 48
    • 27
    • 14
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MNX1.
    Top Product
    Discover our top product MNX1 Primary Antibody
  • 应用备注
    MNX1 antibody can be used for detection of MNX1 by ELISA at 1:62500. MNX1 antibody can be used for detection of MNX1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store MNX1 antibody at -20 °C.
  • 抗原
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    别名
    MNX1 (MNX1 产品)
    别名
    HB9 antibody, HLXB9 antibody, HOXHB9 antibody, SCRA1 antibody, Hlxb9 antibody, MNR2 antibody, hlxb9 antibody, zgc:112174 antibody, motor neuron and pancreas homeobox 1 antibody, motor neuron homeobox transcription factor antibody, MNX1 antibody, mnx1 antibody, Mnx1 antibody
    背景
    MNX1 contains 1 homeobox DNA-binding domain. MNX1 is a putative transcription factor involved in pancreas development and function. Defects in MNX1 are a cause of Currarino syndrome.
    分子量
    40 kDa
    基因ID
    3110
    NCBI登录号
    NP_005506
    UniProt
    P50219
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