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MAGEA11 抗体

MAGEA11 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6290619
发货至: 中国
  • 抗原 See all MAGEA11 抗体
    MAGEA11 (Melanoma Antigen Family A, 11 (MAGEA11))
    适用
    • 40
    • 1
    • 1
    宿主
    • 39
    • 1
    克隆类型
    • 39
    • 1
    多克隆
    标记
    • 19
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MAGEA11 antibody is un-conjugated
    应用范围
    • 37
    • 14
    • 13
    • 13
    • 11
    • 11
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human MAGEA11
    亚型
    IgG
    Top Product
    Discover our top product MAGEA11 Primary Antibody
  • 应用备注
    WB 1:200 - 1:2000
    说明

    Expressed in tumors of several types, such as melanoma, head and neck squamous cell carcinoma, lung carcinoma and breast carcinoma, Expressed in testis, ovary, prostate, cancerous prostate, breast and adrenal tissue

    限制
    仅限研究用
  • 缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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
    储存方法
    Store at -20C. Avoid freeze / thaw cycles.
  • 抗原
    MAGEA11 (Melanoma Antigen Family A, 11 (MAGEA11))
    别名
    MAGEA11 (MAGEA11 产品)
    别名
    MAGEA11 antibody, CT1.11 antibody, MAGE-11 antibody, MAGE11 antibody, MAGEA-11 antibody, melanoma antigen family A, 11 antibody, MAGE family member A11 antibody, Magea11 antibody, MAGEA11 antibody
    背景
    This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80 % sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Two transcript variants encoding different isoforms have been found for this gene.
    分子量
    48.129 kDa
    基因ID
    4110
    UniProt
    P43364
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