單株抗體藥物發現始於識別功能性治療靶點,並評估其在目標疾病中的作用。隨後需闡明該靶點所涉及的分子機制。所有靶點均應具備可成藥性,且能被潛在治療藥物調控。隨著各種基因組工程與雜交瘤技術的出現,這些早期階段已得到簡化,這些技術可用於生物治療性抗体的靶點與先導化合物發現。
搶佔先機
發掘、篩選並驗證與疾病密切相關的新靶點。藥物研發初期所做的抉擇,將直接決定專案成敗。識別最合適且具藥物開發潛力的靶點是成功的關鍵。我們提供完整的基因組級、通路特異性及蛋白質家族靶向篩選工具組,助您高效完成靶點發現。
• 功能基因組學篩選工具用於標靶識別
• 體外工具用於標靶驗證
• 單株抗體生產 •
純化
• 篩選與選擇單株抗體候選物
• 先導化合物優化
• 前臨床模型
• 藥代動力學/藥效動力學與免疫原性
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相關類別
使用我們的CRISPR基因編輯工具,實現目標基因的敲除、敲入、敲除或過量表達。
適用於細胞系、原代細胞、類器官及進階細胞模型的細胞培養基。
實驗室規模、製程規模及工業規模的抗體色譜純化。
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