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。
SLC35A3 Antibody (monoclonal) (M01)
Mouse monoclonal antibody raised against a partial recombinant SLC35A3.
- 产品详情
- 实验流程
Application 
| WB, E |
|---|---|
| Primary Accession | Q9Y2D2 |
| Other Accession | NM_012243 |
| Reactivity | Human |
| Host | mouse |
| Clonality | monoclonal |
| Isotype | IgG2a Kappa |
| Clone Names | 4B6 |
| Calculated MW | 35985 Da |
| Gene ID | 23443 |
|---|---|
| Other Names | UDP-N-acetylglucosamine transporter, Golgi UDP-GlcNAc transporter, Solute carrier family 35 member A3, SLC35A3 |
| Target/Specificity | SLC35A3 (NP_036375, 61 a.a. ~ 113 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
| Dilution | WB~~1:500~1000 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 | SLC35A3 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
Evaluation of SLC35A3 as a candidate gene for human vertebral malformations. Ghebranious N, et al. Am J Med Genet A, 2006 Jun 15. PMID 16691598.Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932.Molecular cloning and functional expression of the human Golgi UDP-N-acetylglucosamine transporter. Ishida N, et al. J Biochem, 1999 Jul. PMID 10393322.Functional role of the glycan cluster of the human immunodeficiency virus type 1 transmembrane glycoprotein (gp41) ectodomain. Fenouillet E, et al. J Virol, 1993 Jan. PMID 8093218.Role of protein N-glycosylation in pathogenesis of human immunodeficiency virus type 1. Montefiori DC, et al. Proc Natl Acad Sci U S A, 1988 Dec. PMID 3264072.
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