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一种纯化5-氨基水杨酸的简单方法。该产品作为底物在酶联免疫吸附测定(ELISA)中的应用。

A simple method for the purification of 5-aminosalicylic acid. Application of the product as substrate in enzyme-linked immunosorbent assay (ELISA).

作者信息

Ellens D J, Gielkens A L

出版信息

J Immunol Methods. 1980;37(3-4):325-32. doi: 10.1016/0022-1759(80)90318-x.

Abstract

Commercially available 5-aminosalicylic acid (5-AS) was recrystallised in the presence of Na2S2O5. A completely colourless solution was obtained when the purified product was dissolved at a concentration of 1 mg/ml in a phosphate buffer containing EDTA and H2O2. No significant increase in absorption was found upon storage for 18 h at 4 degrees C. A 8-fold increase in sensitivity of an enzyme-linked immunosorbent assay for the detection of rotavirus antigens was demonstrated by using the modified substrate solution instead of the conventional substrate solution of crude 5-AS. In addition, P/N values did not significantly change between 2 and 18 h after addition of the substrate, thus rendering the time of reading less critical. No difference in sensitivity of the assay was found between modified 5-AS solution and ortho-phenylenediamine (OPD). However, since OPD requires special care in handling the modified 5-AS solution is preferred for use in routine ELISAs.

摘要

市售的5-氨基水杨酸(5-AS)在焦亚硫酸钠存在下进行重结晶。当纯化后的产物以1mg/ml的浓度溶解于含有乙二胺四乙酸(EDTA)和过氧化氢(H₂O₂)的磷酸盐缓冲液中时,可得到完全无色的溶液。在4℃下储存18小时后,未发现吸光度有显著增加。通过使用改良的底物溶液而非粗制5-AS的常规底物溶液,酶联免疫吸附测定(ELISA)检测轮状病毒抗原的灵敏度提高了8倍。此外,加入底物后2至18小时之间,阳性/阴性(P/N)值无显著变化,因此读数时间的要求降低。改良的5-AS溶液与邻苯二胺(OPD)在该检测的灵敏度上没有差异。然而,由于OPD在处理时需要特别小心,因此改良的5-AS溶液更适合用于常规ELISA。

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