Dystrophin 抗体
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北京 101111
Quick Overview for Dystrophin 抗体 (ABIN8121096)
抗原
See all Dystrophin (DMD) 抗体适用
宿主
克隆类型
标记
应用范围
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原理
- DMD Antibody
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特异性
- DMD Polyclonal Antibody detects endogenous levels of protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- Synthesized peptide derived from part region of human protein
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亚型
- IgG
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anti-Dystrophin (DMD) (AA 346-635) antibody
DMD 适用: 人 IHC, WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Dystrophin (DMD) (AA 114-263) antibodyDMD 适用: 人 IHC, ELISA 宿主: 小鼠 Monoclonal DMD-3242 unconjugated
anti-Dystrophin (DMD) (AA 1-635) antibodyDMD 适用: 人 WB, ELISA, IP 宿主: 小鼠 Monoclonal 3A11 unconjugated
anti-Dystrophin (DMD) (AA 3076-3404) antibodyDMD 适用: 人, 小鼠, 大鼠 IHC, WB, ICC, IHC (fro), FACS 宿主: 兔 Polyclonal unconjugated
anti-Dystrophin (DMD) (AA 114-263) antibodyDMD 适用: 人 IHC, ELISA 宿主: 小鼠 Monoclonal DMD-3241 unconjugated
anti-Dystrophin (DMD) (AA 114-263) antibodyDMD 适用: 人 IHC, ELISA 宿主: 小鼠 Monoclonal DMD-3245 unconjugated
anti-Dystrophin (DMD) (AA 3048-3328) antibodyDMD 适用: 人 IHC, WB 宿主: 兔 Polyclonal unconjugated
anti-Dystrophin (DMD) (AA 253-597) antibodyDMD 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Dystrophin (DMD) antibodyDMD 适用: 人 IHC, ELISA 宿主: 兔 Monoclonal 4B10 unconjugated Recombinant Antibody
anti-Dystrophin (DMD) (AA 3400-3558) antibodyDMD 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC 1:50-300. IF 1:50-200
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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
- Liquid in PBS containing 50 % glycerol, and 0.02 % 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
- Store at -20°C/1 year
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有效期
- 12 months
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- Dystrophin (DMD)
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别名
- DMD
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背景
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Background: dystrophin(DMD) Homo sapiens The dystrophin gene is the largest gene found in nature, measuring 2.4 Mb. The gene was identified through a positional cloning approach, targeted at the isolation of the gene responsible for Duchenne (DMD) and Becker (BMD) Muscular Dystrophies. DMD is a recessive, fatal, X-linked disorder occurring at a frequency of about 1 in 3,500 new-born males. BMD is a milder allelic form. In general, DMD patients carry mutations which cause premature translation termination (nonsense or frame shift mutations), while in BMD patients dystrophin is reduced either in molecular weight (derived from in-frame deletions) or in expression level. The dystrophin gene is highly complex, containing at least eight independent, tissue-specific promoters and two polyA-addition sites. Furthermore, dystrophin RNA is differentially spliced, producing a range of different transcripts, encoding a large set of protein isoforms. Dystrophin (as enc
Gene Name: DMD
Protein Name: Dystrophin
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基因ID
- 1756
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UniProt
- P11532
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途径
- Skeletal Muscle Fiber Development
抗原
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