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ELK Biotechnology p27 (phospho Ser178) rabbit pAb
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ELK Biotechnology p27 (phospho Ser178) rabbit pAb

상품 한눈에 보기

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.

판매단위
pk
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ELK Biotechnology ES4450-100UL p27 (phospho Ser178) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES4450-50UL p27 (phospho Ser178) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology p27 (phospho Ser178) rabbit pAb

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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