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ELK Biotechnology SH-PTP2 (phospho Tyr580) rabbit pAb
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ELK Biotechnology SH-PTP2 (phospho Tyr580) rabbit pAb

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SHP-2 단백질의 Tyr580 인산화 부위를 인식하는 rabbit polyclonal antibody. WB, IHC, IF, ELISA에 사용 가능하며, 다양한 세포 신호 조절 연구에 적합. Human, Mouse, Rat 반응성. -20°C에서 1년 보관.

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pk
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ELK Biotechnology ES1456-100UL SH-PTP2 (phospho Tyr580) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES1456-50UL SH-PTP2 (phospho Tyr580) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology SH-PTP2 (phospho Tyr580) rabbit pAb

제품명

SH-PTP2 (phospho Tyr580) rabbit pAb

제품 개요

이 항체는 인간 SHP-2 단백질의 Tyr580 인산화 부위를 기반으로 제작된 rabbit polyclonal antibody입니다. 단백질 인산화 조절, 세포 신호전달 및 암 관련 연구에 유용합니다.

제품 정보

항목 내용
Alternative Names PTPN11; PTP2C; SHPTP2; Tyrosine-protein phosphatase non-receptor type 11; Protein-tyrosine phosphatase 1D; PTP-1D; Protein-tyrosine phosphatase 2C; PTP-2C; SH-PTP2; SHP-2; Shp2; SH-PTP3
Applications WB; IHC; IF; ELISA
Recommended Dilutions WB: 1/500–1/2000
IHC: 1/100–1/300
ELISA: 1/40000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human SHP-2 around the phosphorylation site of Tyr580 (AA range: 546–595)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 70 kD
Gene ID (Human) 5781
Human Swiss-Prot No. Q06124
Cellular Localization Cytoplasm, Nucleus
Species Reactivity Human, Mouse, Rat

Background

The protein encoded by this gene belongs to the protein tyrosine phosphatase (PTP) family, which regulates various cellular processes such as cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains that act as phospho-tyrosine binding domains, mediating interactions with substrates. It is widely expressed across tissues and plays a key regulatory role in cell signaling events including mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are associated with Noonan syndrome and acute myeloid leukemia (RefSeq, Aug 2016).

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