购物车
全部删除
您的购物车当前为空
Anti-IMPAD1 Polyclonal Antibody 是一种 Rabbit 抗体,靶向 IMPAD1。Anti-IMPAD1 Polyclonal Antibody 可用于 WB。
Anti-IMPAD1 Polyclonal Antibody 是一种 Rabbit 抗体,靶向 IMPAD1。Anti-IMPAD1 Polyclonal Antibody 可用于 WB。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 50 μL | ¥ 1,160 | 5日内发货 | |
| 100 μL | ¥ 1,965 | 5日内发货 | |
| 200 μL | ¥ 2,795 | 5日内发货 |
| 产品描述 | Anti-IMPAD1 Polyclonal Antibody is a Rabbit antibody targeting IMPAD1. Anti-IMPAD1 Polyclonal Antibody can be used in WB. |
| Ig Type | IgG |
| 反应种属 | Mouse (predicted:Human,Rat,Dog,Pig,Cow,Sheep) |
| 应用 | WB |
| 推荐剂量 | WB: 1:500-2000 |
| 抗体种类 | Polyclonal |
| 宿主来源 | Rabbit |
| 亚细胞定位 | Golgi apparatus, trans-Golgi network membrane; Single-pass type II membrane protein. |
| 构建方式 | Hybridoma Polyclonal Antibody |
| 纯化方式 | Protein A purified |
| 性状 | Liquid |
| 缓冲液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 浓度 | 1mg/ml |
| 研究背景 | This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. |
| 免疫原 | KLH conjugated synthetic peptide: human IMPAD1 |
| 抗原种属 | Human |
| 基因名称 | BPNT2 |
| 基因ID | |
| 蛋白名称 | Golgi-resident adenosine 3', 5'-bisphosphate 3'-phosphatase |
| Uniprot ID | |
| 功能 | May play a role in the formation of skeletal elements derived through endochondral ossification, possibly by clearing adenosine 3',5'-bisphosphate produced by Golgi sulfotransferases during glycosaminoglycan sulfation |
| 分子量 | Theoretical: 39 kDa. |
| 储存方式 | Store at 2°C-8°C for 1 month. 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 |