抗结核菌抗体测定，使用酶标法。
方法：采用酶标双抗体夹心法(ELISA法)测定50例感染新生儿和20例非感染新生儿血清gcsf水平。
Methods: We measured the levels of serum G CSF with the method of ELISA in 50 cases of infectious newborns and 20 cases of non infectious ones.
方法采用APAAP桥联酶标法测定外周血t细胞亚群。
Methods t lymphocyte subpopulation in peripheral blood was measured by APAAP method.
方法采用端粒重复序列扩增文件-酶标法（TRAP-ELISA）测定尖锐湿疣皮损中端粒酶的活性，并与正常皮肤和恶性肿瘤对照比较。
Methods The telomerase activity was detected by TRAP( telomeric repeat amplification protocol) -ELISA which based upon PCR amplification of the initial telomerase product and detected by ELISA.
应用亲和酶标组化标记法和免疫组化ABC法，测定106例乳腺癌组织中ER、PR和DAKO—M1水平。
The expression of ER, PR and DAKO-M1 in 106 breast carcinomas were examined by bothaffinitive histochemical and ABC technique.
用快速法检测定值标本和病人血清中的乙肝标志物与常规法比较，无统计学差异，故本增速剂在乙肝酶标诊断中是可以应用的。
Hepatitis B Viral labeles in valued samples and patients sera were detected by the rapid method and the general method comparatively, the result shows that there are no statistics differences.
本试剂盒应用双抗体夹心酶标免疫分析法测定标本中血小板抗体水平。
This assay employs the quantitative sandwich enzyme immunoassay technique. Platelet antigens have been pre-coated onto a microplate.
本试剂盒应用双抗体夹心酶标免疫分析法测定标本中淋巴细胞因子水平。
This assay employs the quantitative sandwich enzyme immunoassay technique. A monoclonal antibody specific for lymphocyte factor has been pre-coated onto a microplate.
本试剂盒应用双抗体夹心酶标免疫分析法测定标本中淋巴细胞因子水平。
This assay employs the quantitative sandwich enzyme immunoassay technique. A monoclonal antibody specific for lymphocyte factor has been pre-coated onto a microplate.
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