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。
CTNNAL1 Antibody (monoclonal) (M05)
Mouse monoclonal antibody raised against a partial recombinant CTNNAL1.
- 产品详情
- 实验流程
Application 
| E |
|---|---|
| Primary Accession | Q9UBT7 |
| Other Accession | NM_003798 |
| Reactivity | Human |
| Host | mouse |
| Clonality | monoclonal |
| Isotype | IgG2a Kappa |
| Clone Names | 2C11 |
| Calculated MW | 81896 Da |
| Gene ID | 8727 |
|---|---|
| Other Names | Alpha-catulin, Alpha-catenin-related protein, ACRP, Catenin alpha-like protein 1, CTNNAL1 |
| Target/Specificity | CTNNAL1 (NP_003789, 277 a.a. ~ 380 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
| Dilution | 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 | CTNNAL1 Antibody (monoclonal) (M05) 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
An approach based on a genome-wide association study reveals candidate loci for narcolepsy. Shimada M, et al. Hum Genet, 2010 Oct. PMID 20677014.Seven placental transcripts characterize HELLP-syndrome. Buimer M, et al. Placenta, 2008 May. PMID 18374411.Alpha-catulin, a Rho signalling component, can regulate NF-kappaB through binding to IKK-beta, and confers resistance to apoptosis. Wiesner C, et al. Oncogene, 2008 Apr 3. PMID 17952117.Wound repair and proliferation of bronchial epithelial cells regulated by CTNNAL1. Xiang Y, et al. J Cell Biochem, 2008 Feb 15. PMID 17647259.The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Gerhard DS, et al. Genome Res, 2004 Oct. PMID 15489334.
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