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- 抗原 See all Anoctamin 5 (ANO5) 抗体
- Anoctamin 5 (ANO5)
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抗原表位
- AA 798-828, C-Term
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适用
- 人, 小鼠
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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 Anoctamin 5 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Enzyme Immunoassay (EIA)
- 特异性
- Recognizes ANO5 (C-term).
- 纯化方法
- Protein A Chromatography followed by peptide affinity purification
- 免疫原
- Synthetic peptide -KLH conjugated between 798~828 amino acids from the C-terminal region of Human ANO5. Genename: ANO5
- 亚型
- Ig Fraction
- Top Product
- Discover our top product ANO5 Primary Antibody
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anti-Anoctamin 5 (ANO5) (AA 792-819), (C-Term) antibody
ANO5 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB22028 unconjugated
anti-Anoctamin 5 (ANO5) (AA 1-300) antibodyANO5 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Anoctamin 5 (ANO5) (2nd Cytoplasmic Loop), (AA 532-544) antibodyANO5 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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ELISA: 1/1,000. Western blotting: 1/100-1/500.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.25 mg/mL
- 缓冲液
- PBS with 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.
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- 抗原
- Anoctamin 5 (ANO5)
- 别名
- ANO5 (ANO5 产品)
- 别名
- gdd1 antibody, tmem16e antibody, MGC82557 antibody, TMEM16E antibody, ano5 antibody, si:dkey-261m9.4 antibody, GDD1 antibody, LGMD2L antibody, 9330162L24 antibody, Gdd1 antibody, Tmem16e antibody, anoctamin 5 L homeolog antibody, anoctamin 5 antibody, anoctamin 5a antibody, ano5.L antibody, ANO5 antibody, ano5a antibody, ano5 antibody, Ano5 antibody
- 背景
- ANO5 is a member of the anoctamin family of transmembrane proteins. This protein is likely a calcium activated chloride channel. Defects in ANO5 are the cause of gnathodiaphyseal dysplasia (GDD), also known as osteogenesis imperfecta with unusual skeletal lesions or gnathodiaphyseal sclerosis. GDD is a rare skeletal syndrome characterized by bone fragility, sclerosis of tubular bones, and cemento-osseous lesions of the jawbone. Patients experience frequent bone fractures caused by trivial accidents in childhood, however the fractures heal normally without bone deformity. The jaw lesions replace the tooth-bearing segments of the maxilla and mandible with fibrous connective tissues, including various amounts of cementum-like calcified mass, sometimes causing facial deformities. Patients also have a propensity for jaw infection and often suffer from purulent osteomyelitis-like symptoms, such as swelling of and pus discharge from the gums, mobility of the teeth, insufficient healing after tooth extraction and exposure of the lesions into the oral cavity.Synonyms: Anoctamin-5, GDD1, Gnathodiaphyseal dysplasia 1 protein, TMEM16E, Transmembrane 16E
- 基因ID
- 203859
- NCBI登录号
- NP_001136121
- UniProt
- Q75V66
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