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[肌酸激酶同工酶MB特异性单克隆抗体的研制与应用]

[Development and application of CK-MB specific monoclonal antibodies].

作者信息

Chen Zimin, Zhou Guoliang, Xu Weiling, Zheng Xiaohong, Tong Xunzhang, Ke Qishen, Song Liuwei, Ge Shengxiang

机构信息

National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Life Sciences, Xiamen University, Xiamen 361102, Fujian, China.

Xiamen Innodx Biotech Co., Ltd., Xiamen 361026, Fujian, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2017 Jan 25;33(1):141-150. doi: 10.13345/j.cjb.160216.

Abstract

The aim of this study is to develop creatine kinase isoenzyme MB (CK-MB) specific monoclonal antibodies (mAb), and characterize the monoclonal antibody and further development of quantitative detection assay for CK-MB. The BALB/c mice were immunized with purchased CK-MB antigen, then monoclonal antibodies were prepared according to conventional hybridoma technique and screened by indirect and capture ELISA method. To identify the epitopes and evaluate the classification, purchased creatine kinase isoenzyme MB (CK-MM/BB/MB) antigen was used to identify the epitopes, with immunoblotting and synthetic CK-MM and CK-BB in different linear epitope. A double antibody sandwich ELISA was applied to screen the mAb pairs for CK-MB detection, and the quantitative detection assay for CK-MB was developed. We used 74 cases of clinical specimens for comparison of our assay with Roche's CK-MB assay. We successfully developed 22 strains of hybridoms against CK-MB, these mAbs can be divided into linear, partial conformational CK-MB, CK-MM or CK-BB cross monoclonal antibody and CK-MB specific reaction with partial conformational monoclonal antibody, and CK-MB quantitative detection assay was developed by using partial conformational monoclonal antibody. The correlation coefficient factor r of our reagent and Roche's was 0.930 9. This study established a screening method for CK-MB partial conformational specific monoclonal antibody, and these monoclonal antibodies were analyzed and an established quantitative detection assay was developed. The new assay had a high concordance with Roche's.

摘要

本研究的目的是开发肌酸激酶同工酶MB(CK-MB)特异性单克隆抗体(mAb),对该单克隆抗体进行表征,并进一步开发CK-MB的定量检测方法。用购买的CK-MB抗原免疫BALB/c小鼠,然后根据传统杂交瘤技术制备单克隆抗体,并通过间接和捕获ELISA方法进行筛选。为了鉴定表位并评估分类,使用购买的肌酸激酶同工酶MB(CK-MM/BB/MB)抗原通过免疫印迹以及不同线性表位中的合成CK-MM和CK-BB来鉴定表位。应用双抗体夹心ELISA筛选用于CK-MB检测的单克隆抗体对,并开发CK-MB的定量检测方法。我们使用74例临床标本将我们的检测方法与罗氏公司的CK-MB检测方法进行比较。我们成功开发了22株抗CK-MB的杂交瘤,这些单克隆抗体可分为线性、部分构象的CK-MB、CK-MM或CK-BB交叉单克隆抗体以及与部分构象单克隆抗体发生特异性反应的CK-MB,并且使用部分构象单克隆抗体开发了CK-MB定量检测方法。我们的试剂与罗氏试剂的相关系数r为0.930 9。本研究建立了CK-MB部分构象特异性单克隆抗体的筛选方法,对这些单克隆抗体进行了分析,并开发了一种成熟的定量检测方法。新方法与罗氏方法具有高度一致性。

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