DTNA 抗体 (AA 692-721)
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Quick Overview for DTNA 抗体 (AA 692-721) (ABIN7876457)
抗原
See all DTNA 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 692-721
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原理
- Dystrobrevin alpha Antibody / DTNA
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纯化方法
- Antigen affinity purified
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免疫原
- A portion of amino acids 692-721 from the human protein was used as the immunogen for the Dystrobrevin alpha antibody.
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亚型
- Ig Fraction
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anti-Dystrobrevin alpha (DTNA) (AA 1-371) antibody
DTNA 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Dystrobrevin alpha (DTNA) (AA 692-721), (C-Term) antibodyDTNA 适用: 人, 小鼠 WB, IF, IHC (p) 宿主: 兔 Polyclonal RB31275 unconjugated
anti-Dystrobrevin alpha (DTNA) antibodyKD Validated DTNA 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 25GB3985 unconjugated
anti-Dystrobrevin alpha (DTNA) (AA 691-721), (C-Term) antibodyDTNA 适用: 人, 小鼠 WB, IF, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Dystrobrevin alpha (DTNA) (AA 1-686) antibodyDTNA 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Dystrobrevin alpha (DTNA) (AA 240-480) antibodyDTNA 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Dystrobrevin alpha (DTNA) antibodyDTNA 适用: 人 WB 宿主: 小鼠 Monoclonal 24GB8130 unconjugated
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应用备注
- The stated application concentrations are suggested starting points. Titration of the Dystrobrevin alpha antibody may be required due to differences in protocols and secondary/substrate sensitivity.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- In 1X PBS, pH 7.4, with 0.09 % sodium azide
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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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储存条件
- -20 °C
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储存方法
- Aliquot the Dystrobrevin alpha antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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- DTNA (Dystrobrevin alpha (DTNA))
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别名
- Dystrobrevin alpha
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背景
- The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
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UniProt
- Q9Y4J8
抗原
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