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- 抗原 See all ALX4 抗体
- ALX4 (ALX Homeobox 4 (ALX4))
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This ALX4 antibody is un-conjugated
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应用范围
- Western Blotting (WB), 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
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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 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) (AA 151-200) antibodyALX4 适用: 人, 小鼠, 大鼠, 犬, Cow, 豚鼠, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (C-Term) antibodyALX4 适用: 人, 犬, Cow, 兔, 马, 豚鼠, 猴, 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
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- 应用备注
- WB 1:1000, FLOW 1:100,
- 说明
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The concentration of the product may vary between diferrent lots.
- 限制
- 仅限研究用
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- 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
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- 抗原
- ALX4 (ALX Homeobox 4 (ALX4))
- 别名
- ALX4 (ALX4 产品)
- 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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