ALX4 抗体
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- 抗原 See all ALX4 抗体
- ALX4 (ALX Homeobox 4 (ALX4))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This ALX4 antibody is un-conjugated
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应用范围
- 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
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- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
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- 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.
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- 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
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Observed_MW: 44 kDa
Calculated_MW: 44 kDa
- 基因ID
- 60529
- UniProt
- Q9H161
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