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ALX4 抗体

ALX4 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7189784
发货至: 中国
  • 抗原 See all ALX4 抗体
    ALX4 (ALX Homeobox 4 (ALX4))
    适用
    • 38
    • 11
    • 8
    • 6
    • 5
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 36
    • 4
    克隆类型
    • 36
    • 4
    多克隆
    标记
    • 21
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ALX4 antibody is un-conjugated
    应用范围
    • 29
    • 17
    • 13
    • 3
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    交叉反应
    人, 小鼠
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of Human ALX4
    亚型
    IgG
    Top Product
    Discover our top product ALX4 Primary Antibody
  • 应用备注
    ELISA:1:1000-1:2000, IHC:1:25-1:100,
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    储存方法
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 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

    Background: 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.

    Aliases: Alx4 antibody, ALX4_HUMAN antibody, Aristaless like homeobox 4 antibody, CRS5 antibody, FND2 antibody, FPP antibody, homeobox protein aristaless like 4 antibody, Homeobox protein aristaless-like 4 antibody, homeodomain transcription factor ALX4 antibody, KIAA1788 antibody, PFM1 antibody, PFM2 antibody

    UniProt
    Q9H161
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