陽性期 的英文怎麼說
中文拼音 [yángxìngqī]
陽性期
英文
positive phase-
Prepotent 5 in virus of afterbirth of large and small shows masculine gender, rheumatism bleb shows masculine gender, it is long - dated infection, have very big effect to be pregnant excuse me
優生五項中巨細胞病毒呈陽性,風濕皰疹呈陽性,是遠期感染,請問對懷孕有很大的影響嗎The respiratory intensity of the contaminated soil decreased by 29. 93 % while ammonification and nitrification increased significantly than that of control soil. 2. extraction and purification of soil microbial total dna a method of extracting soil total dna was developed, and it can extract dna from g + bacteria
二、土壤微生物總dna的提取和純化方法研究為了採用不依賴于培養的16srdna分析的方法研究有機磷農藥長期污染對土壤微生物群落結構的影響,建立了從土壤中提取總dna的方法,並通過改進使適合於對革蘭氏陽性菌的提取。( 2 ) gene flow frequency was reduced as distance from pollen donor increased and a dramatic reduction occurred at about 2 meters. the maximum distance where gene flow was not detected was 50 m for hybrid rice while it was 70 m for ms lines, with an exception that in one of the four ms lines it was detected a frequency of gene flow 2. 8 + 10 - 6 at 150 m for zhong 9a
在開花期主流風向ne的風速為0 . 2 ? 2 . 2m / sec的條件下, 2個雜交稻品種的最大漂流距離為40m ; 4個不育系的基因漂流基本上到60m為止, 70m處基因漂流頻率均降為0 ,僅中9a在150m處發現了1株basta抗性苗,經pcr檢測驗證為陽性。The primary cell propagated 8 times and were small fusiform or triangle and smaller than hepatocytes with larger nucleus and less plasma ; it was 88. 2 % in the growing period of 4 ( superscript th ) generation cells and the stains of alb and ck19 were positive in immunocytochemical
所獲得的原代細胞共傳8代,細胞呈小梭形或三角形,體積較小,胞核較大,而胞漿較少;第4代細胞中進入生長期的細胞約佔88 . 2 % ;免疫細胞化學染色顯示細胞胞質中alb 、 ck19染色陽性。In order to study the regulatory mechanism in gametogenesis of loxoblemmus doenitzi, the special expression of c - kit and c - myc is investigated by immunohistochemical method. the results show that there are kit positive protein granules on the cellular membrane of spermatomeres from metaphase i to anaphase ii, and in the head of mature spermatozoa not only in the testis but also in the spermatheca
結果表明, kit在多伊棺頭蟋精子發生中期至後期的精母細胞膜上有陽性顆粒,在精巢和受精囊內精子頭部殘留的細胞質內也有陽性表達;但在出生后卵子發生過程中,發育中的卵母細胞上無陽性表達。Women with clinical characteristics consistent with a high risk for gdm ( e. g., those with marked obesity, personal history of gdm or delivery of a previous large - forgestation - age infant, glycosuria, polycystic ovary syndrome, or a strong family history of diabetes ) should undergo glucose testing as soon as possible
具有妊娠糖尿病高危因素(如:肥胖、妊娠糖尿病史、曾產巨大兒、過期產、尿糖陽性、多囊卵巢綜合癥、糖尿病家族史)臨床特點的孕婦應該盡快行糖耐量試驗。However, kit protein doesn " t exist in oogenesis after birth. there are also c - myc positive protein granules in the spermatomeres from metaphase i to telophase ii, in the spermatozoa and in the secretory cells of the spermatheca. c - myc protein expresses not in the normal follicles, but in the follicular cells of the apoptotic ones
Myc在處于減數分裂的中期至末期的精母細胞的細胞質或細胞核內呈陽性表達,在減數分裂后形成的精細胞和受精囊囊壁的上皮細胞的細胞質內也有陽性表達:但在出生后的卵子正常發生過程中無陽性表達,然而在凋亡卵泡的濾泡細胞的細胞質內有陽性表達。Using the hprt gene as a positive control, our result suggested that both the testis tissue and the male embryos from which sry transcription can be detected failed to yield any positive results of xist. female embryos at the pronucleus stage and 2 - cell failed to produce any positive result of sry and xist too. while since the 4 - cells period, xist is constantly transcribed until blastocyst stages
然後利用實驗一確定的pcr條件,以hprt為陽性對照,用巢式rt - pcr對小鼠早期胚胎進行xist基因的轉錄分析,結果發現,轉錄sry基因的睪丸組織以及雄性胚胎,從受精卵發育到囊胚的過程中,基本上不轉錄xist基因;不轉錄sry基因的雌性卵母細胞和雌性胚胎,從出現原核開始,到發育至2 -細胞期的過程中, xist基因一直不轉錄,但是,從4 -細胞期開始,一直到孵化前囊胚階段,雌性胚胎都轉錄xist基因。The results demonstrated that prl immunopositive cells were dispersed throughout the adenohypophysis at day 60 of gestation, and prl immunopositive cells arranged in cords or clusters in late gestation
研究結果表明:在胎兒發育的第60天, prl免疫陽性細胞散在或呈索狀分佈於整個腺垂體,而在妊娠後期, prl免疫陽性細胞形成細胞索或細胞團。Detection of antigen - binding affinity of mg7 recombinant phage antibody elisa was repeated to confirm the antigen - binding affinity of positive clones screened out in the former procedure ; these positive phages were examined by restriction analysis ( ecor i and hind iii ) ; competitive elisa was performed to test the inhibitory ratio of these positive clones to the binding affinity of mg7mab and its relevant antigen, the positive dones possessing apparent inhibitory effect were singled out for later use
X陽性克到駛知烘扳原kbbjg )濁對陽性克隆進行限制隴臥賜析( uwi和hedlll )鑒定三用競爭elisatoljmg7重組噬菌體抗體性克隆對mg7單扶與其相應抗原結合忙的喇率,從中j ) ed出對mg7單抗與期眩抗原結合有抑余j效應的克隆用於進一涉研究。The endocrine cells in the digestive and glands of alligator sinensis embryos aged from 8th to 55th day were localized and compared by using immunohistochemical method with thirteen kinds of antiseras of hormone. during the development of pancreas in alligator sinensis embryos, somatostatin ( ss ) immunoreactive ( ir ) cells, 5 - hydroxytryptamine ( 5 - ht ) - ir cells, glucagon ( glu ) - ir cells, epidermal growth factor ( egf ) - ir cells appeared on 18th day. no p53 protein - ir cell, gastrin - ir cell, testosterone - ir cell, chromogranin a - ir cell, vasoactive intestinal polypeptide - ir cell, epithelial membrane antigen - ir cell or insulin - ir cell was found in the pancreas of alligator sinensis embryos
本實驗採用免疫組織化學技術,應用13種不同的抗血清,對孵育時間8 ? 55天揚子鱷胚胎消化道及消化腺內分泌細胞的種類進行鑒別、定位和比較,結果如下:揚子鱷胚胎胰腺中,生長抑素、 5 ?羥色胺、胰高血糖素、表皮生長因子、胰多肽免疫反應陽性細胞出現于第8天; p物質免疫陽性細胞出現于第18天; p53 、胃泌素、睪酮、嗜鉻素a 、血管活性腸肽、上皮膜骯原、胰島素免疫陽性細胞在各期揚子鱷胚胎胰腺中均未發現。Materials and methods : fecal, cloacal and tracheal swabs from different types of poultry were collected in 6 live - bird retail markets once a week. they were inoculated into 9 - 11 days embryonated chicken eggs and incubated in 35 " c for 72 hours. hi and nl assays were performed to detect the subtype of viruses if ha test were positive ( ad ^ 16 ) and contamination test were negative
材料和方法:每星期收集一次標本,收集的標本常規處理, 9 - 11日齡雞胚尿囊腔接種, 35培養72小時,收取尿囊液,血凝陽性( ad 16 )且細菌培養陰性者- 70保存並進一步做hi , ni實驗鑒定亞型。Hybridization bands were detected by southern blot analysis using lea3 gene probe labeled by digoxigenin the result showed that foreign lea3 gene integrated into strawberry genome
2 。對點雜交為陽性的植株進行southernblot分析,轉化植株檢測到了雜交帶,除預期的1In the present study, in order to investigate the effects of endogenous estrogen on the daergic terminals in amy and the daergic neurons in midbrain, fast cyclic voltammetry ( fcv ) was used to examine da release evoked by electrical stimulation from amy of female rats in different phases of estrus cycle, ovx rats and male rats. and tyrosine hydroxylase ( th ) immunohistochemi stry was employed to measure the numbers of daergic neurons of ventral tegmental area ( vta ) and substantia nigra ( snc ) in the rats
因此,為進一步探討大鼠內源性雌激素水平的變化對amyda能神經系統及中腦da能神經元的影響,本工作應用快速周期伏安法( fcv )在體監測了處于動情周期各期雌鼠、 ovx鼠和雄鼠經電刺激誘發的amyda釋放,並應用酪氨酸羥化酶( th )免疫組化方法測定了以上各組大鼠腹側背蓋區( vta ) 、黑質( snc )的th陽性神經元數目。Different amount of copies in different tissues attribute to the different density of positive signals. the result of the experiment suggested that the transgenic animals can be produced by spermatozoa - mediated gene transfer after the entrapment of liposome. and because the exogenous dna occurs losing the segments. partly integration, or existin g outside of genome dna, the rate of chimerism is relatively high
結果表明: ( 1 )脂質體包裹外源基因轉染精子的方法,可將外源基因導入受精卵中,能夠獲得轉基因動物,並得到了較高的轉基因陽性率; ( 2 )精子攜帶的外源dna的整合過程是隨機的,在受精過程和胚胎早期分化過程中可能發生了片段丟失、不完全整合或游離于基因組存在而產生嵌合體。Campaired with the control groups, the absolute weight, grouth index and cell cycle of immune organs, the anae positive rates of t lymphocytes in peripheral blood, the erythrocyte c3brr and cic rosette rates were singnificantly changed in the zinc - deficient and zinc - toxic ducklings. histopathologically, lymphocytes of the immune organs were depleted, degenerated and necrotic in both zinc - deficient and zinc - toxic ducklings
缺鋅和鋅中毒組免疫器官的絕對重量、生長指數、細胞生長周期以及t淋巴細胞anae ~ +陽性率、紅細胞c _ 3b受體花環、免疫復合物花環率與對照組比較差異顯著( p 0 . 05 )或極顯著( p 0 . 01 ) 。In addition, the stomach contained glu - ir cellsn gas - ir cells and vip - ir cells, and the duodenum contained glu - ir cells and gas - ir cells. different endocrine cells varied from one to another in the distribution pattern, the stage of appearance and the number. no glu - ir cell, gas - ir cell or vip - ir cell was found in the oesophagus and no vip - ir cell in the duodenum
另外,胚胎期揚子鱷消化道內分泌細胞的種類和分佈與成體有差異,胚胎期消化道檢出胰高血糖素、胰多肽和p物質免疫陽性細胞,而成體未檢出;胚胎期消化道中胃泌素、血管活性腸肽,生長抑素免疫陽性細胞分佈與成體消化道不同。The present studies aimed to find the responses of neurons and glias in the target and other brain areas of the linear accelerator - irradiated rats. in the first experiment, time - dependent neurons changes in the brain after hemispheric irradiation at an single - fraction maximal dose of 20 gy were observed by investigating the expression of an immediate early gene, fos protein. the results shown : compared with that of the un - radiated rats, the expression of fos protein in the irradiated brain decreased distinctly 24 hours and 1 week after irradiation
首先,利用即刻早期基因fos的表達,做了同一照射劑量( 20gy )照射大鼠半腦后不同存活期間( 1d , 7d , 14d , 2ld , 28d )大鼠全腦神經元動態變化的觀察,發現:受照射后1d 、 7d大鼠腦內各部位fos蛋白表達均明顯減少,隨著時間的延長,其fos免疫反應性細胞數量逐漸增加,照射后28d ,延髓、第四軍醫大學碩士學位論文腦橋內hs免疫陽性細胞數量恢復並超過正常對照組水平,但中腦、間腦及端腦內未恢復到正常對照組水平。Be probably related with the change of gaba releasing in the brain. in order to testify the effect of nos inhibitor and gaba on the regulation of the sleep / waking cycle in adult rats implanted for chronic sleep recordings, the polysomnogram was recorded. we observed whether the sleep - suppressing action of nos inhibitor was affected after the administration of the agonists of gaba receptors by subcutaneous route
本研究採用多導睡眠描記技術和皮下給藥方式,觀察應用gaba受體激動劑后,對nos抑制劑引起的睡眠抑制效應有無影響,同時用免疫組化的方法,觀察應用nos抑制劑后大鼠額葉皮質2區( frz區) gaba免疫反應( gaba一ir )陽性細胞表達的變化,從而探討no和gaba在睡一醒周期調控中的作用。The high specificity of dot - ppa - elisa was proved by the specific blocking test, and also by the cross - reaction test in which the diaphragm did n ' t react with the antibodies against pasteurellosis, streptococcosis, colibacillosis, chlamydiosis, hcv, ppv, brucellosis, prv and foot - mouth disease. the diaphragm has good sensitivity and could detect some salmonella - positive test serum which has been diluted to 1 : 2048. stored at 4 for at least 6 months or at 10 - 25 " c for 4 months, the sensitivity and specif icity of the diaphragm did n ' t change, so it has good stability
本研究制備的診斷膜片特異性強:不與豬衣原體病、豬口蹄疫病、豬大腸桿菌病、豬布氏桿菌病、豬瘟、豬偽狂犬病、豬細小病毒病、豬巴氏桿菌病、豬鏈球菌病的陽性血清發生交叉反應;診斷膜片具有良好的敏感性,能夠檢測到1 : 2048稀釋的動物試驗陽性血清;膜片的保存期長,在10 25可保存4個月、 4條件下至少可保存6個月其靈敏度不變。分享友人