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MAGE-Like 2 抗体 (C-Term)

MAGEL2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN929381
发货至: 中国
  • 抗原 See all MAGE-Like 2 (MAGEL2) 抗体
    MAGE-Like 2 (MAGEL2)
    抗原表位
    • 15
    • 7
    • 3
    • 1
    C-Term
    适用
    • 33
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 33
    克隆类型
    • 33
    多克隆
    标记
    • 8
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MAGE-Like 2 antibody is un-conjugated
    应用范围
    • 13
    • 13
    • 11
    • 6
    • 6
    • 5
    • 3
    • 1
    Western Blotting (WB)
    纯化方法
    Purified
    免疫原
    MAGEL2 antibody was raised in rabbit using the C terminal of MAGEL2 as the immunogen
    Top Product
    Discover our top product MAGEL2 Primary Antibody
  • 应用备注
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    说明

    MAGEL2 Blocking Peptide, catalog no. 33R-6559, is also available for use as a blocking control in assays to test for specificity of this MAGEL2 antibody

    限制
    仅限研究用
  • 状态
    Lyophilized
    浓度
    Lot specific
    缓冲液
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    注意事项
    Avoid repeated freeze/thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • 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
    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. Synonyms: Polyclonal MAGEL2 antibody, Anti-MAGEL2 antibody, MAGE-like 2 antibody, NDNL1 antibody, nM15 antibody.
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