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ALX4 抗体

ALX4 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7260673
发货至: 中国
  • 抗原 See all ALX4 抗体
    ALX4 (ALX Homeobox 4 (ALX4))
    适用
    • 39
    • 10
    • 7
    • 6
    • 5
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 36
    • 5
    克隆类型
    • 36
    • 5
    多克隆
    标记
    • 22
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ALX4 antibody is un-conjugated
    应用范围
    • 29
    • 18
    • 13
    • 4
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human ALX4 (NP_068745.2).
    亚型
    IgG
    Top Product
    Discover our top product ALX4 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    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 -20°C. Avoid freeze / thaw cycles.
  • 抗原
    ALX4 (ALX Homeobox 4 (ALX4))
    别名
    ALX4 (ALX4 产品)
    别名
    im:7142878 antibody, zgc:162606 antibody, alx4 antibody, FND2 antibody, lst antibody, ALX homeobox 4b antibody, ALX homeobox 4a antibody, ALX homeobox 4 antibody, aristaless-like homeobox 4 antibody, alx4b antibody, alx4a antibody, ALX4 antibody, Alx4 antibody
    背景
    This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2), an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism, suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS), a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart.
    分子量

    Observed_MW: 44 kDa

    Calculated_MW: 44 kDa

    基因ID
    60529
    UniProt
    Q9H161
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