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。
Anti-Cytokeratin 13 Antibody
- 产品详情
- 实验流程
Application 
| WB, IHC |
|---|---|
| Primary Accession | P13646 |
| Reactivity | Human, Mk |
| Host | Rabbit |
| Clonality | Polyclonal |
| Calculated MW | 49588 Da |
| Gene ID | 3860 |
|---|---|
| Other Names | Keratin, type I cytoskeletal 13; Cytokeratin-13; CK-13; Keratin-13; K13 |
| Target/Specificity | KLH-conjugated synthetic peptide encompassing a sequence within the center region of human Cytokeratin 13. The exact sequence is proprietary. |
| Dilution | WB~~WB (1/500 - 1/1000) IHC~~1:100~500 |
| Format | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
| Storage | Store at -20 °C.Stable for 12 months from date of receipt |
For Research Use Only. Not For Use In Diagnostic Procedures.
| Name | KRT13 (HGNC:6415) |
|---|---|
| Function | Structural component of intermediate filaments in mucosal stratified squamous epithelia. Forms heteropolymers with the type II keratin KRT4, assembling into keratin intermediate filament networks that provides structural integrity and mechanical stability of the mucosal epithelium (PubMed:7493031). Contributes to postnatal tongue mucosal cell homeostasis and tissue organization in response to mechanical stress, potentially through regulation of the G1/S phase cyclins CCNE1 and CCNE2 (By similarity). |
| Tissue Location | Expressed in some epidermal sweat gland ducts (at protein level) and in exocervix, esophagus and placenta |
Research Areas
Application Protocols
Provided below are standard protocols that you may find useful for product applications.
REFERENCES
Schulz P.,et al.Biochem. Biophys. Res. Commun. 162:1522-1527(1989).
Mischke D.,et al.Nucleic Acids Res. 17:7984-7984(1989).
Kuruc N.,et al.Differentiation 42:111-123(1989).
Waseem A.,et al.Gene 215:269-279(1998).
Ota T.,et al.Nat. Genet. 36:40-45(2004).
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