OPTIMIZATION OF THE COVALENT CONJUGATING PROCEDURE (NAIO4) OF HORSERADISH-PEROXIDASE TO ANTIBODIES FOR USE IN ENZYME-LINKED-IMMUNOSORBENT-ASSAY

被引:53
作者
TSANG, VCW
GREENE, RM
PILCHER, JB
机构
[1] Immunology Branch, Division of Parasitic Diseases, National Center for Infectious Disease, Centers for Disease Control and Prevention, Public Health Services, U.S. Department of Health and Human Service, Atlanta, GA, 30341-
来源
JOURNAL OF IMMUNOASSAY | 1995年 / 16卷 / 04期
关键词
PEROXIDASE; CONJUGATE; IMMUNOASSAY; ELISA; HIV; IMMUNOBLOT;
D O I
10.1080/15321819508013570
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The procedure for covalent conjugation of horseradish peroxidase (POD) to goat anti-human IgG (GAHG) molecules was systematically optimized in terms of reactant molar ratio, time of reaction, pH, and temperature. The optimum conjugation procedure was defined by the conditions that produced an enzyme-labeled Ab with the highest specific activity in immunosorbent assays for normal human IgG (NHIgG). The best conditions are: Sodium meta-periodate (NaIO4) to Ab molar ratio during oxidation is 40:1; time of oxidation is 5 min at 37 degrees C; oxidation reaction is conducted at pH 5.0; the molar ratio of POD:GAHG is 6:1; the conjugation time is 24 h at 4 degrees C; and the optimal conjugation pH is 10.0. A conjugate constructed under these conditions is capable of generating 1.8 and 12.6 times more specific signals (Delta A(650nm)/min) than the best and worst commercial conjugates, respectively.;This conjugate is also able to detect NHIgG at a concentration of 2.25 x 10(-13) M, a sensitivity 25 times that achieved by most comparable commercial products in identical assays.
引用
收藏
页码:395 / 418
页数:24
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