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MAGEA10 抗体

MAGEA10 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7237346
发货至: 中国
  • 抗原 See all MAGEA10 抗体
    MAGEA10 (Melanoma Antigen Family A, 10 (MAGEA10))
    适用
    • 34
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 33
    • 1
    克隆类型
    • 34
    多克隆
    标记
    • 12
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MAGEA10 antibody is un-conjugated
    应用范围
    • 17
    • 16
    • 13
    • 13
    • 8
    • 5
    • 3
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human MAGEA10
    亚型
    IgG
  • 应用备注
    WB 1:1000-1:5000, IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.3 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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 -20°C. Avoid freeze / thaw cycles.
  • 抗原
    MAGEA10 (Melanoma Antigen Family A, 10 (MAGEA10))
    别名
    MAGEA10 (MAGEA10 产品)
    别名
    MAGEA10 antibody, CT1.10 antibody, MAGE10 antibody, RGD1563693 antibody, MAGEA11 antibody, MAGE family member A10 antibody, melanoma-associated antigen 10 antibody, melanoma antigen family A, 10 antibody, putative MAGE domain-containing protein MAGEA13P antibody, MAGEA10 antibody, LOC509805 antibody, Magea10 antibody, LOC492173 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. Alternative splicing results in multiple transcript variants.
    分子量
    41 kDa
    UniProt
    P43363
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