放射式的
1.A Study on the Radiate Measure Way Applied in Different Specifications the Places of Track and Field
2.A univalent organic radical with composition C3H7, derived from propane.
3.The BMSCs from normal Kungming mice were cultured in vitro with the method of Dexter. The expression of interleukin-6 on the levels of protein and mRNA were detected by the uses of radio-immunity assay(RIA) and the reverse transcription polymerase chain reaction(RT-PCR) respectively. PDTC and dexamethasone, two different inhibitors of nuclear factor-kappa B, were used as controls.
5.We studied the effects of Asl on insulin and C-peptide by radioi-mmunoassay We injected three different concentrations of Asl liquores into wistars by intraperitoneal injection the contents ofinsulin and C-peptide were measured at weeks 3, 4 and 5 We discovered that the contents of insulin and C-peptide were significantly different between the experiment group and control group (P＜0.05).
6.The results of Flow Cytometry showed the cells were arrested at G0-G1 phase and the cells in the S phase were significantly decreased;
7.Four (CA)_n repeats located in introns 44, 45, 49 and 50 of the dystrophin gene were evaluated in Chinese. These loci are highly polymorphic, with polymorphism information contents of 0.872, 0.772, 0.870 and 0.718, respectively. All four loci can be easily amplified and labelled using 2 duplex PCR reactions with a-~(32)P-dCTP and can be detected by denaturing polyacrylanile gel electrophoresis.
8.Study the specific action of rhAS and its receptor was performed on the model of HMEC-1, S180 tumor and Matrigel by flow cytometry, rhAS-Sepharose 4B affinity chromatography, 99Tcm-rhAS imaging, radioautography and histomorphology.
9.The blood samples were collected from pituitary portal vessels and jugular by surgery during the middle luteal phase or early follicular phase in she goats. GnRH in pituitary blood samples and LH and FSH in jugular ones were measured respectively by RIA.
10.Method:Used AFP which purified from human cord serum,act on human hepatoma Bel7402cell which cultured in vitro. Utilized the MTT counts,cell cycle phase analysis with flow cytomtry and 3 H-thymidine deoxyribonucleotide( 3 H-TdR)incorporation.
