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ELK Biotechnology Cyclin D2 (phospho Thr280) rabbit pAb
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ELK Biotechnology Cyclin D2 (phospho Thr280) rabbit pAb

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Cyclin D2 단백질의 Thr280 인산화 부위를 인식하는 rabbit polyclonal antibody. WB, IHC, IF, ELISA에 적합하며, 세포주기 G1/S 전이 연구에 활용 가능. 인간, 마우스, 랫트 반응성. -20°C에서 1년 보관.

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pk
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ELK Biotechnology ES7912-100UL Cyclin D2 (phospho Thr280) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7912-50UL Cyclin D2 (phospho Thr280) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Cyclin D2 (phospho Thr280) rabbit pAb

Cyclin D2 (phospho Thr280) rabbit pAb

제품 정보

항목 내용
Product Name Cyclin D2 (phospho Thr280) rabbit pAb
Alternative Names CCND2; G1/S-specific cyclin-D2
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500–1/2000
Immunohistochemistry: 1/100–1/300
ELISA: 1/10000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human Cyclin D2 around the phosphorylation site of Thr280 (AA range: 240–289)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 40 kDa
Gene ID (Human) 894
Human Swiss-Prot No. P30279
Cellular Localization Nucleus; Cytoplasm; Nuclear membrane. Cyclin D–CDK4 complexes accumulate at the nuclear membrane and translocate into the nucleus via interaction with KIP/CIP family members. Isoform 2: Cytoplasm
Species Reactivity Human; Mouse; Rat

Background

The protein encoded by this gene belongs to the highly conserved cyclin family, characterized by periodic protein abundance through the cell cycle. Cyclins regulate CDK kinases, and distinct expression/degradation patterns ensure proper mitotic timing. Cyclin D2 forms a complex with CDK4 or CDK6, acting as a regulatory subunit essential for G1/S transition. It interacts with and phosphorylates the tumor suppressor protein Rb. Knockout studies in mice indicate essential roles in ovarian granulosa and germ cell proliferation. High expression levels are observed in ovarian and testicular tumors. Mutations in this gene are associated with megalencephaly.

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