ALX4 抗体 (Middle Region)
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北京 101111
Quick Overview for ALX4 抗体 (Middle Region) (ABIN950384)
抗原
See all ALX4 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 256-283, Middle Region
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特异性
- This antibody reacts to ALX4.
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交叉反应 （详细）
- Species reactivity (tested):Human.
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纯化方法
- Affinity chromatography on Protein A
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免疫原
- KLH conjugated synthetic peptide between 256-283 amino acids from the Central region of human ALX4
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亚型
- Ig Fraction
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anti-ALX Homeobox 4 (ALX4) (AA 249-275) antibody
ALX4 适用: 人 WB, FACS, CUT&RUN 宿主: 兔 Polyclonal RB28072 unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人 WB, IHC, IF, IHC (p) 宿主: 小鼠 Monoclonal 6B3 unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 2F2 unconjugated
anti-ALX Homeobox 4 (ALX4) (AA 1-220) antibodyALX4 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (AA 112-216) antibodyALX4 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (AA 31-80) antibodyALX4 适用: 人, 小鼠, 犬, Cow, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (N-Term) antibodyALX4 适用: 人, 大鼠, 犬, 马, 猴, Drosophila melanogaster WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (AA 151-200) antibodyALX4 适用: 人, 小鼠, 大鼠, 犬, Cow, 豚鼠, Pig WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS containing 0.09 % (W/V) sodium azide as preservative
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储存液
- Sodium azide
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注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- ALX4 (ALX Homeobox 4 (ALX4))
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别名
- ALX4
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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
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基因ID
- 60529
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NCBI登录号
- NP_068745
抗原
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