| 產(chǎn)品編號 | bs-14208R |
| 英文名稱 | DCUN1D4 Rabbit pAb |
| 中文名稱 | DCN1樣蛋白4抗體 |
| 別 名 | DCN1 like protein 4; DCN1, defective in cullin neddylation 1, domain containing 4(S. cerevisiae); DCN1, defective in cullin neddylation 1, domain containing 4; DCN1-like protein 4; DCNL4_HUMAN; DCUN1 domain containing protein 4; DCUN1 domain-containing protein 4; DCUN1D 4; Dcun1d4; Defective in cullin neddylation protein 1-like protein 4; KIAA0276. |
| 研究領(lǐng)域 | 腫瘤 細胞生物 免疫學(xué) |
| 抗體來源 | Rabbit |
| 克隆類型 | Polyclonal |
| 克 隆 號 | |
| 交叉反應(yīng) | (predicted: Human,Mouse,Rat,Pig,Sheep,Cow,Dog,Horse) |
| 產(chǎn)品應(yīng)用 | IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 34 kDa |
| 檢測分子量 | |
| 細胞定位 | 細胞核 |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human DCUN1D4: 201-292/292 |
| 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 | 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 |
The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Similarity: Contains 1 DCUN1 domain SWISS: Q92564 Gene ID: 23142 Database links: Entrez Gene: 23142 Human Entrez Gene: 100737 Mouse Omim: 612977 Human SwissProt: Q92564 Human SwissProt: Q8CCA0 Mouse Unigene: 605388 Human Unigene: 220312 Mouse |
