DMD抗体DMD兔多抗抗体Muscular dystroph
y Duchenne and Becker types antibody抗体DMD Antibody, Biotin conjugated抗体- ￥880 - 1320
- CUSABIO
- CN
- CSB-PA006963LD01HU
- 2025年07月11日
- ELISA
- Rabbit
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant Human Dystrophin protein (3400-3558AA)
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
Polyclonal
- 标记物：
Biotin
- 适应物种：
Human
- 保质期：
6个月
- 抗原来源：
Homo sapiens (Human)
- 目录编号：
P11532
- 级别：
优
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 宿主：
Rabbit
- 应用范围：
ELISA
- 浓度：
>95%,Protein G purified
- 靶点：
DMD
- 抗体英文名：
DMD Antibody, Biotin conjugated
- 抗体名：
BMD antibody;CMD3B antibody;DMD antibody;DMD_HUMAN antibody;Duchenne muscular dystrophy protein antibody;Dystrophin antibody;Muscular dystrophy Duchenne and Becker types antibody
- 规格：
100μg/50μg
| 规格： | 100μg | 产品价格： | ￥1320.0 |
|---|---|---|---|
| 规格： | 50μg | 产品价格： | ￥880.0 |
保存缓冲液
Preservative: 0.03% Proclin 300Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
功能
Anchors the extracellular matrix to the cytoskeleton via F-actin. Ligand for dystroglycan. Component of the dystrophin-associated glycoprotein complex which accumulates at the neuromuscular junction (NMJ) and at a variety of synapses in the peripheral and central nervous systems and has a structural function in stabilizing the sarcolemma. Also implicated in signaling events and synaptic transmission.风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Duchenne and Becker Muscular Dystrophy
The two forms of dystrophin-associated muscular dystrophies, known as Duchenne and Becker muscular dystrophy (DMD/BMD; OMIM 310200) are caused by genetic defects in the huge DMD gene (79 exons), located at Xp21 and coding for the 427-kDa
DNA-Based Techniques for Detection of Carriers of Duchenne and Becker Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is the most frequent muscle disease in children. The incidence of DMD is 1/4000 live-born males; one-third of the patients are the result of new mutation. DMD, a progressive, lethal, X-linked neuromuscular
DNA- Based Prenatal Diagnosis for Duchenne and Becker Muscular Dystrophy
Progressive muscle wasting, which leads to severe disability and early death, make Duchenne and Becker muscular dystrophies (DMD/BMD) highly distressing disorders to both patient and family. Diagnosis in pregnancy, therefore, is frequently
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