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ALX4 抗体 (Middle Region)

ALX4 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN950384
发货至: 中国
  • 抗原 See all ALX4 抗体
    ALX4 (ALX Homeobox 4 (ALX4))
    抗原表位
    • 7
    • 6
    • 6
    • 6
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 256-283, Middle Region
    适用
    • 39
    • 11
    • 8
    • 6
    • 5
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    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
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    特异性
    This antibody reacts to ALX4.
    交叉反应 (详细)
    Species reactivity (tested):Human.
    纯化方法
    Affinity chromatography on Protein A
    免疫原
    KLH conjugated synthetic peptide between 256-283 amino acids from the Central region of human ALX4
    亚型
    Ig Fraction
    Top Product
    Discover our top product ALX4 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.25 mg/mL
    缓冲液
    PBS containing 0.09 % (W/V) sodium azide as preservative
    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.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 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.Synonyms: Homeobox protein aristaless-like 4, KIAA1788
    基因ID
    60529
    NCBI登录号
    NP_068745
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