癌症的基本特征包括细胞增殖、血管生成、迁移、凋亡逃避机制和细胞永生等。找到癌症发生过程中这些通路的关键标记物和对应的抗体用于检测至关重要。
为您推荐一个泛素化位点预测神器——泛素化分析工具，可以为您的蛋白的泛素化位点作出预测和评分。
细胞自噬受体图形绘图工具为你的蛋白的细胞受体结合位点作出预测和评分，识别结合到自噬通路中的蛋白是非常重要的，便于让我们理解自噬在正常生理、病理过程中的作用，如发育、细胞分化、神经退化性疾病、压力条件下、感染和癌症。
IFNE1 Antibody (monoclonal) (M01)
Mouse monoclonal antibody raised against a partial recombinant IFNE1.
- 产品详情
- 实验流程
Application 
| WB, IP, E |
|---|---|
| Primary Accession | Q86WN2 |
| Other Accession | NM_176891 |
| Reactivity | Human |
| Host | Mouse |
| Clonality | monoclonal |
| Isotype | IgG2a Kappa |
| Clone Names | 3B8 |
| Calculated MW | 24414 Da |
| Gene ID | 338376 |
|---|---|
| Other Names | Interferon epsilon, IFN-epsilon, Interferon epsilon-1, IFNE, IFNE1 |
| Target/Specificity | IFNE1 (NP_795372, 109 a.a. ~ 208 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
| Dilution | WB~~1:500~1000 IP~~N/A E~~N/A |
| Format | Clear, colorless solution in phosphate buffered saline, pH 7.2 . |
| Storage | Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. |
| Precautions | IFNE1 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures. |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
REFERENCES
Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study. Melton PE, et al. Hum Mol Genet, 2010 Sep 15. PMID 20601674.Dengue hemorrhagic fever is associated with polymorphisms in JAK1. Silva LK, et al. Eur J Hum Genet, 2010 Jun 30. PMID 20588308.Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations. Yang XR, et al. Fam Cancer, 2010 Jun 24. PMID 20574843.[Anti-HIV effects of IFN-tau in human macrophages: role of cellular antiviral factors and interleukin-6] Maneglier B, et al. Pathol Biol (Paris), 2008 Nov-Dec. PMID 18842358.Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease. Schunkert H, et al. Circulation, 2008 Apr 1. PMID 18362232.
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