
ELK Biotechnology p27 (phospho Ser178) rabbit pAb
인간 및 마우스 반응성을 가진 p27 (phospho Ser178) rabbit polyclonal antibody. 세포주기 조절 관련 단백질 검출에 적합하며, IHC, IF, ELISA 등에 사용 가능. 합성 펩타이드 기반 면역원으로 제작되어 높은 특이성과 재현성을 제공.
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ELK Biotechnology p27 (phospho Ser178) rabbit pAb
제품 개요
p27 (phospho Ser178) rabbit polyclonal antibody는 인간 p27 Kip1 단백질의 Ser178 인산화 부위를 인식하도록 제작된 항체입니다. 세포주기 조절 및 단백질 위치 변화 연구에 활용됩니다.
제품 정보
| 항목 | 내용 |
|---|---|
| Product name | p27 (phospho Ser178) rabbit pAb |
| Alternative Names | CDKN1B; KIP1; Cyclin-dependent kinase inhibitor 1B; Cyclin-dependent kinase inhibitor p27; p27Kip1 |
| Applications | IHC; IF; ELISA |
| Recommended Dilutions | Immunohistochemistry: 1/100 - 1/300 ELISA: 1/5000 Not yet tested in other applications |
| Immunogen | Synthesized peptide derived from human p27 Kip1 around the phosphorylation site of Ser178 (AA range: 144–193) |
| Host | Rabbit |
| Storage | -20°C / 1 year |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Gene ID (Human) | 1027 |
| Human Swiss-Prot No | P46527 |
| Species Reactivity | Human; Mouse |
세포 내 위치 (Cellular Localization)
- Nucleus, Cytoplasm, Endosome
- Nuclear and cytoplasmic in quiescent cells
- AKT- or RSK-mediated phosphorylation on Thr-198 enables cytoplasmic translocation and promotes cell cycle progression
- UHMK1 phosphorylation on Ser-10 also induces cytoplasmic translocation and progression
- Phosphorylation on Ser-10 facilitates nuclear export
- Phosphorylation of Tyr-88 and Tyr-89 triggers nuclear import
- Colocalizes at the endosome with SNX6, leading to lysosomal degradation (By similarity)
배경 (Background)
This gene encodes a cyclin-dependent kinase inhibitor that shares limited similarity with CDKN1A/p21. The protein binds to and prevents activation of cyclin E-CDK2 or cyclin D-CDK4 complexes, controlling cell cycle progression at G1. Its degradation, triggered by CDK-dependent phosphorylation and ubiquitination by SCF complexes, is required for transition from quiescence to the proliferative state. Mutations in this gene are associated with multiple endocrine neoplasia type IV (MEN4). [RefSeq, Apr 2014]
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