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- deoxyuridine triphospate 三磷酸脫氧尿苷
- TdT-mediated dUTP nick end labeling kit, TUNEL No. 公司末端標記試劑盒。
- Methods: Using HE staining and TdTmediated dUTP nick endlabeling (TUNEL) to detect cardiac myocyte apoptosis in spontaneously hypertensive rats. 方法：運用HE染色及TdT介導的dUTP缺口末端標記法（TUNEL）檢測自發(fā)性高血壓大鼠心肌細胞凋亡。
- By using terminal deoxynuceotidy transferase mediated dUTP nick end labeling(TUNEL),apoptotic cells were detected in situ in 50 ECAC specimens. 采用脫氧核糖核酸末端轉移酶介導的缺口末端標記技術(shù) (TUNEL) ,對其中 4 0例賁門(mén)癌組織中凋亡的TIL及腫瘤細胞進(jìn)行觀(guān)察。
- Apoptotic cells were identified and quantified by the terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) method. 采用TUNEL免疫組織化學(xué)法檢測鼻咽癌組織放射治療前、后腫瘤細胞凋亡。
- Methods To reasarch using MTT assay,the tdt-mediated dUTP biotin end labeling（TUNEL） method and immunocytochemistry Ki-67 staining method etc. 方法 用MTT比色法、原位細胞凋亡檢測法（TUNEL法）及免疫細胞化學(xué)Ki-67染色法等進(jìn)行研究。
- Cardiomyocyte apoptosis was detected with in situ terminal deoxynucleotidyl transferase(TdT) mediated dUTP nick end labeling(TUNEL) and DNA gel electrophoresis. 末端脫氧核糖核酸轉移酶介導的dUTP切口末端標記技術(shù)(TUNEL)和DNA凝膠電泳檢測心肌細胞凋亡。
- Methods Replicated the hypothyroid rat model with propylthiouracil (PTU),and then detected the positive cells of PCD in sections by TdT-mediated dUTP nick end labeling. 方法 用丙基硫氧嘧啶（ P T U）復制甲狀腺功能低下的大鼠動(dòng)物模型，然后用原位末端標記方法檢測 P C D 陽(yáng)性細胞。
- Both Annexin-V-FITC/PI FACS and TUNEL(TdT-mediated dUTP nick-end labeling) analysis indicate that GLP-1 can inhibit the apoptosis induced by FFA(P<0.05). Annexin-v/PI流式測定及TUNEL法測定均表明GLP-1能抑制FFA誘導的細胞凋亡(FFA組與FFA+GLP-1組比較;P<0.;05);
- METHODS The adenosine triphospate(ATP)-based tumor chemosensitivity assay (ATP-TCA) was used to examine the growth inhibition of NACC cell treated with different concentration Radix Astragali injection. 方法以不同濃度的黃芪作用于NACC細胞,應用三磷酸腺苷腫瘤化療藥敏試驗(ATPTCA)法測定黃芪注射液對NACC細胞的體外增殖抑制作用;
- Apoptotic cells were assessed by terminal deoxynucleotidyl transferase-mediated dUTP nick end-labelling (TUNEL) as well as by immunostaining of single-stranded DNA (ssDNA). 借助于末端脫氧核苷酸轉移酶介導dUTP缺口末端標記法(TUNEL)如同經(jīng)由單鏈DNA免疫染色技術(shù)一樣對凋亡細胞進(jìn)行分析評估。
- The apoptosis of lymphocytes and nerve cells causing by Avian Encophalomyelitis Vivus (AEV-NH937) was examined using pathological technology,flow cytometer and terminal deoxynucleotidyl transterase mediated dUTP nick endlabeling(TUNEL). 本實(shí)驗主要采用病理組織學(xué)方法、流式細胞儀檢測技術(shù)、末端標記技術(shù)等手段進(jìn)行檢測 ,探討禽腦脊髓炎病毒引起 SPF雛雞淋巴細胞和神經(jīng)細胞凋亡變化。
- Using terminal deoxynuceotidy transferase mediated dUTP nick end labeling (TUNEL) , apoptotic cells were detected in situ in 40 ECAC specimens, Results:The expression of FasL protein was detected in all 50 ECAC examined. 采用脫氧核糖核酸末端轉移酶介導的缺口末端標記技術(shù)(TUNEL),對50例賁門(mén)癌組織中凋亡的TIL及腫瘤細胞進(jìn)行觀(guān)察。 結果50例賁門(mén)癌組織FasL蛋白表達程度不等。
- Apoptotic smooth muscle cells in pulmonary arteries were detected by TdT mediated dUTP biotin nick end labeling ( TUNEL ), and the expression of Fas protein by pulmonary artery smooth muscle cells was detected using immunohistochemistry technique. 通過(guò)末端轉移酶介導的dUTP切口末端標記法 (TUNEL)檢測肺動(dòng)脈平滑肌細胞凋亡 ,并以免疫組織化學(xué)方法研究肺動(dòng)脈平滑肌細胞Fas表達。
- Methods By use of the method of terminal deoxynucleotidyl (TdT) mediated dUTP nick ending labelling (TdT mediated dUTP nick ending labelling)which is adopted to detect DNA splitting,we labelled apoptosis gastric epithelial cell. 方法 采用檢測DNA裂解的末端脫氧核苷酸轉移酶 (TdT)介導的dUTP缺口末端標記法 (TUNEL) ,在原位標記凋亡的胃上皮細胞。
- deoxyuridine monophosphate(dUMP) 脫氧尿苷一磷酸
- After actinomycin D treatment and cellular DNA electrophoresis and detection of TUNEL(TdT mediated bio dUTP nick endlabeling), Sf9 35 cells were found to be resistant to apoptosis induced by actinomycin D. 經(jīng)放線(xiàn)菌素D處理后的細胞核酸電泳和TdT介導bio?DUTP缺口末端標記（TUNEL）試劑盒檢測，證實(shí)Sf9?35具有抗凋亡特性。
- deoxyuridylate(deoxyuridine monophosphate) 脫氧尿苷一磷酸
- Methods Model of vasoligation and vasostomy in male rat was established, and then ter- minal deoxynucleotidyl transferase-mediated dUTP nick labelling technique to detect the apoptosis of spermato- genic cells at 4, 8, 12, 16 weeks after vasostomy. 方法 以雄性 SD大鼠為研究對象 ,建立輸精管阻斷及阻斷后復通模型 ,采用 DNA缺口原位標記凋亡細胞方法 ,觀(guān)察大鼠生精細胞在輸精管復通后 4、8、12及 16周的凋亡狀況。
- deoxyuridylic acid(deoxyuridine monophosphate) 脫氧尿苷一磷酸
