| 產(chǎn)品編號(hào) | bs-7927R |
| 英文名稱 | SIPA1L2 Rabbit pAb |
| 中文名稱 | 信號(hào)誘導(dǎo)增殖相關(guān)蛋白1樣蛋白2抗體 |
| 別 名 | SI1L2_HUMAN; Signal induced proliferation associated 1 like protein 2; Signal-induced proliferation-associated 1-like protein 2; SIPA1 like protein 2; SIPA1-like protein 2; SIPA1L2; SPAL2; KIAA1389. |
| 研究領(lǐng)域 | 細(xì)胞生物 信號(hào)轉(zhuǎn)導(dǎo) 細(xì)胞周期蛋白 細(xì)胞分化 G蛋白信號(hào) |
| 抗體來(lái)源 | Rabbit |
| 克隆類型 | Polyclonal |
| 克 隆 號(hào) | |
| 交叉反應(yīng) | Rat (predicted: Human,Mouse,Rabbit,Sheep,Cow,Dog) |
| 產(chǎn)品應(yīng)用 | IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 190 kDa |
| 檢測(cè)分子量 | |
| 細(xì)胞定位 | 細(xì)胞核 細(xì)胞漿 |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human SIPA1L2: 251-350/1722 |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| PubMed | PubMed |
| 產(chǎn)品介紹 |
SIPA1L2 is a 1,722 amino acid protein that contains one PDZ (DHR) domain and one Rap-GAP domain, and exists as two alternatively spliced isoforms. The gene that encodes SPA-L2 consists of approximately 163,594 bases and maps to human chromosome 1q42.2. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. Similarity: Contains 1 PDZ (DHR) domain. Contains 1 Rap-GAP domain. SWISS: Q9P2F8 Gene ID: 57568 Database links: Entrez Gene: 57568 Human Omim: 611609 Human SwissProt: Q9P2F8 Human SwissProt: Q80TE4 Mouse Unigene: 268774 Human Unigene: 271668 Mouse Unigene: 463243 Mouse Unigene: 44190 Rat |
| 產(chǎn)品圖片 |
Paraformaldehyde-fixed, paraffin embedded (Rat brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (SIPA1L2) Polyclonal Antibody, Unconjugated (bs-7927R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
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