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CAS No. : 205923-56-4
MCE 國際站:Cetuximab
產(chǎn)品活性:Cetuximab (C225) 是一種人源 IgG1 單克隆抗體,,能夠抑制 EGFR,SPR 方法測得 Cetuximab 對 EGFR 的 Kd 值為 0.201 nM,;Cetuximab 具有高效的抗腫瘤作用,。
研究領(lǐng)域:Antibody-drug Conjugate/ADC Related | JAK/STAT Signaling | Protein Tyrosine Kinase/RTK
作用靶點:Radionuclide-Drug Conjugates (RDCs) | EGFR
In Vitro: Cetuximab (C225) is a monoclonal antibody that inhibits epidermal growth factor receptor (EGFR), with a Kd of 0.201 nM for soluble EGFR by SPR. Cetuximab also exhibits a Kd of 0.147 nM for EGFR in fixed A431 cells by ELISA.
Cetuximab (C225; 30 nM) time-dependently inhibits the proliferation of SCC-1, SCC-11B, SCC-38, and SCC-13Y cells after treatment for 8 d. Cetuximab (30 nM) causes G0/G1 arrest, induces apoptosis, and reduces Rb, p27KIP1, Bcl-2, and Bax expression in SCC-13Y cells. Cetuximab (30 nM) also enhances radiosensitivity and increases radiation-induced apoptosis in SCC-13Y cells.
In Vivo: Cetuximab (1 mg/injection) has effect on the tumour volume but the effect is more pronounced on UT-SCC-14 xenografts. In UT-SCC-14 xenografts, Cetuximab significantly reduces the expression of EGFR, pEGFR and Ki67. Cetuximab significantly decreases the expression in the MCT1 and GLUT1 cells but differences are more pronounced in UT-SCC-14 xenografts.
相關(guān)產(chǎn)品:Antibody Inhibitor Library | Osimertinib | Trastuzumab | Gefitinib | Erlotinib | Trastuzumab deruxtecan | Afatinib | Lapatinib | Genistein | AG490 | Rituximab | Trastuzumab emtansine | Tucatinib | Neratinib | Amivantamab | Disitamab vedotin | Pertuzumab | Dacomitinib | AG-1478 | Panitumumab | Patritumab | Lazertinib | NSC 228155 | Rosopatamab | Sapitinib | Zanidatamab | Almonertinib
熱門產(chǎn)品線:重組蛋白 | 藥物篩選 | 天然產(chǎn)物 | 熒光染料 | PROTAC | 同位素標(biāo)記物
Trending products:Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Dye Reagents | PROTAC | Isotope-Labeled Compounds
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