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ELK Biotechnology p27 (phospho Ser10) rabbit pAb
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ELK Biotechnology p27 (phospho Ser10) rabbit pAb

상품 한눈에 보기

인산화된 Ser10 부위를 인식하는 p27 rabbit polyclonal antibody로, 인간, 생쥐, 랫트에 반응합니다. Western blot과 ELISA에 적합하며 세포주기 조절 연구에 활용됩니다. -20°C에서 1년 보관 가능.

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pk
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ELK Biotechnology ES1378-100UL p27 (phospho Ser10) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES1378-50UL p27 (phospho Ser10) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology p27 (phospho Ser10) rabbit pAb

ELK Biotechnology p27 (phospho Ser10) rabbit pAb

제품 개요

본 항체는 인간 p27 Kip1 단백질의 Ser10 인산화 부위를 인식하는 rabbit polyclonal antibody입니다. 세포주기 조절 및 p27 관련 신호전달 연구에 적합합니다.

제품 정보

항목 내용
Product Name p27 (phospho Ser10) rabbit pAb
Alternative Names CDKN1B; KIP1; Cyclin-dependent kinase inhibitor 1B; Cyclin-dependent kinase inhibitor p27; p27Kip1
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/10000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human p27 Kip1 around phosphorylation site of Ser10 (AA range: 1–50)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
GeneID (Human) 1027
Human Swiss-Prot No. P46527
Species Reactivity Human; Mouse; Rat

세포 내 위치 (Cellular Localization)

Nucleus, Cytoplasm, Endosome.
In quiescent cells, p27 is both nuclear and cytoplasmic. AKT- or RSK-mediated phosphorylation on Thr-198 promotes cytoplasmic translocation and cell cycle progression.
Phosphorylation on Ser-10 by UHMK1 facilitates nuclear export and cell cycle progression.
Phosphorylation on Tyr-88 and Tyr-89 induces nuclear translocation.
Colocalization at endosomes with SNX6 leads to lysosomal degradation (By similarity).

Background

This gene encodes a cyclin-dependent kinase inhibitor (CDKN1B/p27), which shares limited similarity with CDKN1A/p21.
The protein binds to and inhibits cyclin E-CDK2 or cyclin D-CDK4 complexes, controlling cell cycle progression at G1 phase.
Degradation of p27, triggered by CDK-dependent phosphorylation and ubiquitination by SCF complexes, is essential for transition from quiescence to proliferation.
Mutations in CDKN1B are associated with multiple endocrine neoplasia type IV (MEN4).
[provided by RefSeq, Apr 2014]

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