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MAGE-Like 2 抗体 (N-Term)

MAGEL2 适用: 人, 兔, Cow, 犬, Pig WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2788252
发货至: 中国
  • 抗原 See all MAGE-Like 2 (MAGEL2) 抗体
    MAGE-Like 2 (MAGEL2)
    抗原表位
    • 15
    • 8
    • 2
    • 1
    N-Term
    适用
    • 28
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 兔, Cow, 犬, Pig
    宿主
    • 28
    克隆类型
    • 28
    多克隆
    标记
    • 9
    • 2
    • 2
    • 2
    • 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
    • 13
    • 7
    • 6
    • 6
    • 3
    • 1
    Western Blotting (WB)
    序列
    MQGLFYRPQG SSKERRTSSK ERRAPSKDRM IFAATFCAPK AVSAARAHLP
    预测反应
    Cow: 83%, Dog: 100%, Human: 100%, Pig: 88%, Rabbit: 100%
    产品特性
    This is a rabbit polyclonal antibody against MAGEL2. It was validated on Western Blot.
    纯化方法
    Affinity Purified
    免疫原
    The immunogen is a synthetic peptide directed towards the N terminal region of human MAGEL2
    Top Product
    Discover our top product MAGEL2 Primary Antibody
  • 应用备注
    Optimal working dilutions should be determined experimentally by the investigator.
    说明

    Antigen size: 529 AA

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    Lot specific
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 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.
    Alias Symbols: NDNL1, nM15
    Protein Interaction Partner: VPS35, VPS26A, USP7, TRIM27, UBC,
    Protein Size: 529
    分子量
    58 kDa
    基因ID
    54551
    NCBI登录号
    NM_019066
    UniProt
    Q9UJ55
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