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- 抗原 See all DTNA 抗体
- DTNA (Dystrobrevin alpha (DTNA))
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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 DTNA antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human DTNA
- 亚型
- IgG
- Top Product
- Discover our top product DTNA Primary Antibody
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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) (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
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- 应用备注
- WB 1:500 - 1:2000
- 说明
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Highly expressed in brain, skeletal and cardiac muscles, and expressed at lower levels in lung, liver and pancreas, Isoform 2 is not expressed in cardiac muscle, Isoform 7 and isoform 8 are only expressed in muscle
- 限制
- 仅限研究用
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- 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 -20C. Avoid freeze / thaw cycles.
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- 抗原
- DTNA (Dystrobrevin alpha (DTNA))
- 别名
- DTNA (DTNA 产品)
- 别名
- adtn antibody, atnb antibody, MGC146484 antibody, 2210407P21Rik antibody, A0 antibody, Dtn antibody, a-DB-1 antibody, adbn antibody, D18S892E antibody, DRP3 antibody, DTN antibody, DTN-A antibody, LVNC1 antibody, Dtna-ps1 antibody, RGD1561985 antibody, dystrobrevin alpha antibody, dystrobrevin, alpha antibody, DTNA antibody, dtna antibody, LOC100195747 antibody, Dtna antibody
- 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.
- 分子量
- 83.901 kDa
- 基因ID
- 1837
- UniProt
- Q9Y4J8
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