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MAGE-Like 2 抗体

MAGEL2 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7191360
发货至: 中国
  • 抗原 See all MAGE-Like 2 (MAGEL2) 抗体
    MAGE-Like 2 (MAGEL2)
    适用
    • 32
    • 2
    • 2
    • 2
    • 2
    • 1
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    • 1
    宿主
    • 32
    克隆类型
    • 32
    多克隆
    标记
    • 7
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    • 1
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    • 1
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    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
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    This MAGE-Like 2 antibody is un-conjugated
    应用范围
    • 13
    • 13
    • 10
    • 6
    • 5
    • 5
    • 3
    • 1
    ELISA, Western Blotting (WB)
    交叉反应
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of Human MAGEL2
    亚型
    IgG
  • 应用备注
    ELISA:1:1000-1:2000, WB:1:200-1:1000,
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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
    -20 °C,-80 °C
    储存方法
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 抗原
    MAGE-Like 2 (MAGEL2)
    别名
    MAGEL2 (MAGEL2 产品)
    别名
    NDNL1 antibody, nM15 antibody, MAGEL2 antibody, Mage-l2 antibody, ns7 antibody, MAGE family member L2 antibody, melanoma antigen, family L, 2 antibody, MAGEL2 antibody, Magel2 antibody
    背景

    Background: Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS.

    Aliases: MAGEL2 antibody, NDNL1 antibody, MAGE-like protein 2 antibody, Necdin-like protein 1 antibody, Protein nM15 antibody

    UniProt
    Q9UJ55
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