Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/21098
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    標題: C-反應蛋白多株抗體之製備與純化
    Production and Purification of Polyclonal Antibodies Against C-reactive Protein
    作者: 周淑芬
    謝東文
    陳弘立
    貢獻者: 生物科技系
    關鍵字: C-反應蛋白
    多株抗體
    酵素連結免疫分析法
    C-reactive protein
    Polyclonal antibodies
    Enzyme-linked immunosorbent assay (ELISA)
    日期: 2006
    上傳時間: 2009-04-24 13:49:29 (UTC+8)
    摘要: 本研究目的在使用 C-反應蛋白 (C-reactive protein, CRP) 腹腔免疫 ICR 小鼠,來生產 C-反應蛋白之多株抗體 (C-reactive protein polyclonal antibodies, anti-CRP)。將高度免疫 (hyperimmune) 之 ICR 小鼠,注射 0.5 mL pristine 後,再間隔兩週注射 106 個 NS-1 骨髓癌細胞。收集 ICR 小鼠所產生之腹水及血清,利用 HitrapTM rProtein A column 來純化多株抗體,並進一步分析已純化 anti-CRP 之抗體效價及其專一性。本研究以間接型酵素連結免疫分析法 (enzyme-linked immunosorbent assay, ELISA) 測定 anti-CRP 之效價。實驗結果顯示,多株抗體 anti-CRP 的效價為 1:3,125。可測得 C-反應蛋白最低濃度為 5 ng/mL,CRP 濃度範圍由 5 ng/mL 至 100 μg/mL 與波長 405nm 之吸光值呈良好線性關係,檢測濃度範圍可謂相當廣。
    The aim of this study was to produce polyclonal antibodies against C-reactive protein (anti-CRP). ICR mice was immunized intraperitoneally with C-reactive protein (CRP) for four to five times every four weeks. Hyperimmune ICR mouse produced anti-CRP after injecting with 0.5 mL pristane, and injected with NS-1 myeloma cells two weeks later. Ascites and serum were collected from ICR mice, and anti-CRP was purified by using HitrapTM rProtein A column, and determination of the titer and specificity of anti-CRP using indirect enzyme-linked immunosorbent assay (ELISA). The results showed the titer of anti-CRP was 1:3,125, and low cross-reaction. A linear relationship existed between absorbance at 405 nm (A405) and CRP concentrations in the range from 5 ng/mL to 100 μg/mL. The detection range was very wide.
    显示于类别:[嘉南學報] 32 期 (2006)
    [生物科技系(所)] 期刊論文

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