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ALX4 抗体

ALX4 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 2F2 unconjugated
产品编号 ABIN2716017
发货至: 中国
  • 抗原 See all ALX4 抗体
    ALX4 (ALX Homeobox 4 (ALX4))
    适用
    • 39
    • 11
    • 8
    • 6
    • 5
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 37
    • 4
    小鼠
    克隆类型
    • 37
    • 4
    单克隆
    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), Flow Cytometry (FACS)
    产品特性
    Homo sapiens ALX homeobox 4 (ALX4)
    纯化方法
    Purified from mouse ascites fluids by affinity chromatography
    免疫原
    Full length human recombinant protein of human ALX4(NP_068745) produced in HEK293T cell.
    克隆位点
    2F2
    亚型
    IgG1
    Top Product
    Discover our top product ALX4 Primary Antibody
  • 应用备注
    WB 1:1000, FLOW 1:100,
    说明

    The concentration of the product may vary between diferrent lots.

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.5-1.0 mg/mL
    缓冲液
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
    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
  • 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
    44.1 kDa
    基因ID
    60529
    NCBI登录号
    NM_021926
    HGNC
    60529
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