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别名 δSarcoglycan, δ Sarcoglycan, SGD, SGCDP, SGCD_HUMAN, SGCD, SG delta, Sarcoglycan delta (35 kDa dystrophin associated glycoprotein), Placental delta sarcoglycan, MGC22567, LGMD2F, Dystrophin associated glycoprotein delta sarcoglycan, dSarcoglycan, Delta-SG, Delta-sarcoglycan, deltaSarcoglycan, DAGD, d Sarcoglycan, CMD1L, 35DAG, 35 kDa dystrophin-associated glycoprotein, 35 kDa dystrophin associated glycoprotein
Anti-delta Sarcoglycan Antibody (5T99) 是一种 Rabbit 抗体,靶向 delta Sarcoglycan。Anti-delta Sarcoglycan Antibody (5T99) 可用于 IHC,IP,WB。
Anti-delta Sarcoglycan Antibody (5T99) 是一种 Rabbit 抗体,靶向 delta Sarcoglycan。Anti-delta Sarcoglycan Antibody (5T99) 可用于 IHC,IP,WB。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 50 μL | ¥ 1,480 | 5日内发货 | |
| 100 μL | ¥ 2,490 | 5日内发货 |
| 产品描述 | Anti-delta Sarcoglycan Antibody (5T99) is a Rabbit antibody targeting delta Sarcoglycan. Anti-delta Sarcoglycan Antibody (5T99) can be used in IHC,IP,WB. |
| 别名 | δSarcoglycan, δ Sarcoglycan, SGD, SGCDP, SGCD_HUMAN, SGCD, SG delta, Sarcoglycan delta (35 kDa dystrophin associated glycoprotein), Placental delta sarcoglycan, MGC22567, LGMD2F, Dystrophin associated glycoprotein delta sarcoglycan, dSarcoglycan, Delta-SG, Delta-sarcoglycan, deltaSarcoglycan, DAGD, d Sarcoglycan, CMD1L, 35DAG, 35 kDa dystrophin-associated glycoprotein, 35 kDa dystrophin associated glycoprotein |
| Ig Type | IgG |
| 克隆号 | 5T99 |
| 反应种属 | Human |
| 验证活性 | 1. Western blot analysis of delta Sarcoglycan on human lung cells lysates using anti- delta Sarcoglycan antibody at 1/500 dilution. 2. Immunohistochemical analysis of paraffin-embedded human stomach cancer tissue using anti- delta Sarcoglycan antibody. Counter stained with hematoxylin. ![]() ![]() |
| 应用 | IHCIPWB |
| 推荐剂量 | WB: 1:500-2000; IHC: 1:50-200; IP: 1:10-50 |
| 抗体种类 | Monoclonal |
| 宿主来源 | Rabbit |
| 构建方式 | Recombinant Antibody |
| 纯化方式 | ProA affinity purified |
| 性状 | Liquid |
| 缓冲液 | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
| 研究背景 | Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix. Defects in SGCD are the cause of limb-girdle muscular dystrophy type 2F (LGMD2F) [MIM:601287]. LGMD2F is an autosomal recessive disorder. Defects in SGCD are the cause of cardiomyopathy dilated type 1L (CMD1L) [MIM:606685]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. |
| 偶联 | Unconjugated |
| 免疫原 | Recombinant Protein |
| Uniprot ID |
| 分子量 | Theoretical: 35 kDa. |
| 储存方式 | Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
| 运输方式 | Shipping with blue ice. |
| 存储 | store at low temperature | -20°C for 1 year |