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通过高效液相色谱法制备具有抗体活性的绵羊和牛免疫球蛋白

Preparation of sheep and cattle immunoglobulins with antibody activity by high-performance liquid chromatography.

作者信息

Schmerr M J, Goodwin K R, Lehmkuhl H D, Cutlip R C

出版信息

J Chromatogr. 1985 Jun 19;326:225-33. doi: 10.1016/s0021-9673(01)87448-3.

Abstract

High-performance anion-exchange chromatography (HPIEC) and high-performance size-exclusion chromatography (HPSEC) were used to purify serum IgM and IgG from sheep and cattle. Pooled serum from normal cattle and sheep and serum from sheep, infected with two different viruses, were prepared for HPIEC by chromatography on CM-Affi-Gel Blue. After HPIEC, fractions containing IgG and IgM were pooled and concentrated and further purified by HPSEC. The purity of fractions from HPIEC and HPSEC were evaluated by immunoelectrophoresis, protein-A-Sepharose affinity chromatography, and sodium dodecyl sulphate-polyacrylamide gel electrophoresis. Monoclonal antibody specific for bovine IgG2 was used to assay for IgG2 and IgG2 contamination of other fractions. The antibody activity to ovine adenovirus 5 and to ovine progressive pneumonia virus was assayed by neutralization and immunodiffusion. Antibody activity was retained against both viruses in the fractions containing IgG1 and IgM. This high-performance liquid chromatography procedure was a rapid preparative method to produce specific immunoglobulins and could be used to evaluate the purity of immuno-reagents.

摘要

采用高效阴离子交换色谱法(HPIEC)和高效尺寸排阻色谱法(HPSEC)从绵羊和牛血清中纯化免疫球蛋白M(IgM)和免疫球蛋白G(IgG)。将正常牛和羊的混合血清以及感染两种不同病毒的绵羊血清,通过CM-亲和凝胶蓝柱层析制备用于HPIEC的样品。经过HPIEC后,收集含有IgG和IgM的组分,进行浓缩,并通过HPSEC进一步纯化。通过免疫电泳、蛋白A-琼脂糖亲和色谱法和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳对HPIEC和HPSEC所得组分的纯度进行评估。使用针对牛IgG2的单克隆抗体检测IgG2以及其他组分中IgG2的污染情况。通过中和试验和免疫扩散法检测针对绵羊腺病毒5和绵羊进行性肺炎病毒的抗体活性。在含有IgG1和IgM的组分中,针对两种病毒的抗体活性均得以保留。这种高效液相色谱方法是一种快速制备特定免疫球蛋白的方法,可用于评估免疫试剂的纯度。

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