Establishment of Quantitative Assay for Human Erythrocyte Pyrimidine 5'-Nucleotidase Content by Double Antibody Sandwich ELISA
- Author:
Zhu-Lin PAN
1
,
2
;
Qian SHEN
;
Jin-Ying LI
;
Bi-He MIN
;
Ding-Wei GU
;
Xiao-Ping XU
;
Hong-Mei LI
;
Xian ZHANG
Author Information
1. Department of Hematology and Laboratory, Changhai Hospital, The Second Military Medical Univessity, Shanghai 200433, China
2. Department of Emergency, The 106 Hospital, Jinan Military Region, Jinan 250022, China.
- Publication Type:Journal Article
- From:
Journal of Experimental Hematology
2001;9(4):368-371
- CountryChina
- Language:Chinese
-
Abstract:
For exploring pathogenesis of pyrimidine 5'-nucleotidase (P5'N) deficiency, a quantitative assay method for human erythrocyte pyrimidine 5'-nucleotidase was established. The specific substrate uridine monophosphate (UMP) of P5'N was used as ligand. The UPM-ADH-Sepharose 4B affinity column was prepared. P5'N of human erythrocyte was purified by ammonium sulfate fractionation and precipitation, ion chromatography and affinity chromatography. Rabbit anti-human P5'N antibody was acquired by immunizing rabbits with purified P5'N. Using rabbit anti-human antibody as the coated anti-body and HRP-rabbit anti-human antibody as demonstrated anti-body, the double antitody sandwich ELISA for quantitative assay of human erythrocyte P5'N was established after square rank trial, antigen blocked trial and antigen substituted test. Results showed that the titer of rabbit anti-human erythrocyte was 1:4 and the sensitivity of double antibody sandwich ELISA was 5 ng/ml. Its blocking rate was more than 95% and the rate of substitution less than 30%. The content of P5'N was (71.77 + 10.98) ng/mg NHP in normal human erythrocyte. A new ELISA method for quantitative determination of human erythrocyte P5'N was first established. It not only had high specificity and sensitivity but also could assay the minimun content of P5'N as 5 - 20 ng/ml. It could be a suitable method for large sample in clinics.
