抗结核菌抗体测定，使用酶标法。
方法采用单克隆抗体桥联酶标法。
Method The respiratory tract viruses were detected by monoclonal antibody bridge-linked ELISA.
再用免疫荧光法或酶标法鉴定。
Uses the immunity fluorescence method or the enzyme sign law again appraises.
免疫酶标法检测犬脑组织狂犬病毒的实验研究。
Experimental study on the detection of rabies virus in caninie brain tissues of the dog with ELISA.
铂金版elisa试剂盒使用前有必要洗涤酶标板吗？
IS it necessary to wash the Platinum ELISA plates before usage?
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.
漆酶构成的生物检测器主要有两种：漆酶电极和漆酶酶标。
Laccase is mainly applied to two aspects of biomonitor: one side is enzyme electrode; the other side is enzyme marker.
采用免疫酶标技术显示出伊贝母愈伤组织细胞内的微管网络。
The microtubule network of fritillary callus cell was showed through immunoenzymological technique.
结果在迷走神经下节和交感干神经节上发现HRP酶标细胞。
It is discovered that in the ganglia of sympathetic trunk there are some HRP enzyme-marked cells.
本文主要介绍《MB-40型酶标检测仪》的设计依据及设计要点。
This paper mainly introduces design consideration and key points of the model MB-40 ELISA microplate reader.
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.
并对酶标抗原浓度、血清保存时间与阳性率的关系及抗原保存期限作了观察。
The relationship among concentration of enzyme-labelled antigen, serum reservation duration, positive rate and reservation duration of antigen were observed.
用已纯化兔抗人CEA和AFP的抗体分别与辣根过氧化物酶结合制得酶标抗体。
The enzyme labelled antibodies are made from purified rabbit antibodies against human CEA and AFP and linked with peroxidase using O-phenylene diamine as a substrate.
通过聚合链反应或ELISA酶标法，已发现25例以上的人类样本为裂谷热阳性。
More than 25 human samples have been found positive for RVF by PCR or ELISA.
通过聚合链反应或ELISA酶标法测试，共有超过25例人类样本被证实为裂谷热阳性。
More than 25 human samples have proved positive for Rift Valley fever by PCR or ELISA testing.
目的：在酶标板上进行DNA探针杂交，评价其在检测临床标本中结核杆菌的应用价值。
Objective: To assess the value of PCRDNA probe in detecting mycobacterium tuberculosis in clinical samples.
而在辣根氧化物酶标显色时，相同条件下光谱自编码微球的检测灵敏度62.5倍于96孔酶标比色板。
The sensitivity of HRP enzyme conjugated antibody in ELISA matrix tests on optical self-encoding microbeads proves 62.5 times higher than on 96-wells ELISA plate.
在对抗原包被量、酶标抗体浓度、血清稀释度进行优化的基础上，对本方法的灵敏度和特异度进行评价。
After the parameters of the assay were optimized, the reproducibility and the sensitivity and specificity of the method were evaluated.
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.
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.
系统感染长叶车前花叶病毒的青菜叶片叶柄分别作冰冻切片，运用免疫酶标技术对叶片叶柄内的病毒进行显色定位。
Chinese cabbage leaf blade and leaf stalk of Brassica Chinensis systematically infected with Ribgrass Mosaic virus was separately made by the freezing cut transection.
方法：用APAAP免疫酶标法检测10例经il - 2激活的急性白血病患者骨髓细胞相关抗原标记及活化过程中的变化。
Methods: 10 patients with acute leukemia were selected and their bone marrow cell related antigen labeling and activation process changes activated by IL-2 were detected by APAAP method.
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.
方法对102例急性白血病患者的骨髓或外周血直接涂片，应用13种白细胞系列单克隆抗体，ABC免疫酶标法进行免疫学分型。
Methods The immunophenotyping of 102 cases with AL were detected by 13 leukon monoclonal antibodies with direct smear of peripheral blood or bone marrow and ABC-AP staining method.
方法：采用端粒重复序列扩增文件酶标法（TRAP-ELISA），对32例AML和非恶性血液系统疾病骨髓细胞端粒酶活性检测。
Methods:The telomerase activity was determined in bone marrow cells from 32 patients of acute myeloid leukemia and non-malignant hematogic disease by TRAP-ELISA.
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.
我们通过长期的实践摸索，对各种类型的酶标仪进行了系统的测试和论证，初步建立了一套为保证酶标分析仪工作可靠而制定的性能评价和校准方法。
We test and demonstrate all type of enzyme micro-plate reader, and finally establish a calibration method for guaranteeing the stability and reliability of enzyme micro-plate reader.
用辣根过氧化物酶标记后，作为酶标二抗检测HCV阴性和阳性标准血清各4 0份，阴性符合率为97.5 % ，阳性符合率为95 % ，可用于抗HCV的ELISA检测。
HRP IgG was used to test 40 HCV negative and 40 HCV positive standard serum. The negative conformity rate is 97.5% and positive conformity rate is 95%. It can be used for ELISA test of anti HCV.
用辣根过氧化物酶标记后，作为酶标二抗检测HCV阴性和阳性标准血清各4 0份，阴性符合率为97.5 % ，阳性符合率为95 % ，可用于抗HCV的ELISA检测。
HRP IgG was used to test 40 HCV negative and 40 HCV positive standard serum. The negative conformity rate is 97.5% and positive conformity rate is 95%. It can be used for ELISA test of anti HCV.
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