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WNT7A 抗体

WNT7A 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6292487
发货至: 中国
  • 抗原 See all WNT7A 抗体
    WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))
    适用
    • 28
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    • 2
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    • 2
    • 1
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    小鼠, 大鼠
    宿主
    • 35
    克隆类型
    • 35
    多克隆
    标记
    • 11
    • 3
    • 2
    • 2
    • 2
    • 2
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    • 2
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    • 1
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    This WNT7A antibody is un-conjugated
    应用范围
    • 22
    • 9
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human WNT7A
    亚型
    IgG
    Top Product
    Discover our top product WNT7A Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    说明

    Expression is restricted to placenta, kidney, testis, uterus, fetal lung, and fetal and adult brain

    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
    WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))
    别名
    WNT7A (WNT7A 产品)
    别名
    wnt7a antibody, AI849442 antibody, Wnt-7a antibody, px antibody, tw antibody, Xwnt-7a antibody, wnt-7a antibody, wnt7a-A antibody, Wnt family member 7A antibody, wingless-type MMTV integration site family, member 7Aa antibody, wingless-type MMTV integration site family, member 7A antibody, wingless-type MMTV integration site family member 7A S homeolog antibody, WNT7A antibody, wnt7aa antibody, Wnt7a antibody, wnt7a.S antibody
    背景
    This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is involved in the development of the anterior-posterior axis in the female reproductive tract, and also plays a critical role in uterine smooth muscle pattering and maintenance of adult uterine function. Mutations in this gene are associated with Fuhrmann and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromes.
    分子量
    39.005 kDa
    基因ID
    7476
    UniProt
    O00755
    途径
    WNT signaling, Stem Cell Maintenance, Asymmetric Protein Localization
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