after-inhibition 中文意思是什麼

after-inhibition 解釋
后抑制
  • after : adv 在後；繼后；后來。 follow after 跟著。 look before and after 瞻前顧后，前思後想。 soon after ...
  • inhibition : n. 1. 禁止，阻止。2. 【心理學】壓制，抑制（作用），心障。3. 【英法】訴訟停止命令。4. 【宗教】教權停止命令。5. 【化學】抑制（作用）。
  1. Heamagglutination tests were applied to detect virus in allantoic fluid of chicken embryos which were infected by b95 gathered from the vaccinated chickens " cloacal and oral cavity. the results show that the virus may be detected from 2 days to 11 days after the chicken being vaccinated. the hi antibodies were measured by heamagglutination inhibition tests. there is no significant difference between the immunized and the control chickens which were fed in one case. chickens were immunized with b95 by different immunization meathods or with different vaccines by the same meathod. lt is demonstrated that eyedrop, drinking water, spray or muscle injection all can stimulate good effects, but eyedrop and spray seem to be the best meathods. b95 immunized chicken have relatively higher hi titers and it also can last for a longer time than others

    但如果兩者相隔10天以上免疫， b95免疫不受h120的影響；如果同時免疫b95和h120 ，加大b95的免疫劑量也能獲得良好的免疫效果。用棉拭子采b95免疫雞口腔、泄殖腔的分泌液，檢測其中病毒的存在，結果免疫后2 11天雞口腔和泄殖腔中均有病毒的存在，說明b95免疫雞帶毒時間長。研究結果表明， b95具有不受母源抗體干擾、 hi抗體產生快、水平高、持續時間長、同居擴散性強等特點，因此b95是一株優良的、具開發前景的新的新城疫疫苗株。
  2. Effect of erk on 17 - estradiol - induced inhibition of vsmc proliferation in rats after vascular injury

    雌二醇抑制大鼠血管損傷后平滑肌細胞增殖中的作用
  3. They are pkc, pka, mek1 in erk pathway, mekk1 in sapk / jnk, p38 in p38 pathway, the three latter pathways all belong to the map kiiiase pathway. the inhibition of pkc decreases the proliferation after the il - 16 treatments, which hint its role in proliferation signal transduction

    結果表明，加入pkc的抑制劑，強烈抑制了所有濃度16處理下細胞的增殖，暗示pkc在u一16與cd4結合后，可能傳遞了增殖相關信號，它的存在是jllrk盯細胞的生長增殖必須的。
  4. Studies of the crystal structure of endostatin have shown a compact globular fold, with one face particularly rich in arginine residues acting as a heparin - binding epitope, this site was recently shown to be involved in the inhibition of induced angiogenesis. experimental studies show that recombinant endostatin specifically inhibits the proliferation of endothelial cells in a dosedependent fashion. recombinant endostatin from bacteria is largely insoluble, but still efficient in arresting tu mor growth after injection into mice. intermittent therapy with recombinant bacterially produced endostatin reduces several experimental tumors, including lewis lung carcinoma, to a dormant state. no sign of drug induced resistance has been reported and, in the original study, the treatment dormancy appeared to persist even when therapy was discontinued. sowe regard endostatin as a promising anti - tumor drug

    許多研究表明重組內皮抑素特異性抑制內皮細胞增殖，而且這種抑制作用呈劑量依賴性。細菌表達產物內皮抑素大部分以不溶形式存在，將這種混懸液注射治療老鼠仍可以抑制腫瘤生長。于小鼠皮下重復注射內皮抑素重組蛋白，幾乎完全抑制鼠lewis肺癌等多種腫瘤生長，並無耐藥性產生，即使中斷治療腫瘤也不再復發。
  5. The mechanisms of such treatment have been proposed as inhibition of proliferation and angiogenesis, as well as induction of differentiation and apoptosis, as has been tested by various in vivo and in vitro experiments. in our experiments, it has also been demonstrated that after the treatment of arsenic trioxide, the k562 cells has undergone major morphological changes, which included nuclear shrinkage, membrane bleb and scattered apoptotic bodies. dna gel electrophoresis also discovered that the typical " dna ladder " phenomena in the treatment group, while the control group showed the regular genomic banding

    我們在實驗中觀察到as _ 2o _ 3作用人紅白血病k562細胞后，細胞生長明顯變緩，部分細胞出現皺縮、染色質濃聚及胞膜起泡現象，部分細胞胞膜破裂，在其周圍有緻密的凋亡小體出現， dna電泳出現典型的凋亡「梯狀」帶，提示as _ 2o _ 3能有效抑制k562細胞生長，誘導k562細胞凋亡。
  6. The activity of urease is hard to recover entirely with regeneration solution after contacting inhibitors for many times. for this reason, a renewable urease biosensor is highly desired. in chapter 3, a renewable potentiometric urease inhibition biosensor based on self - assembled gold nanoparticles has been developed for the determination of mercury ions

    2 .重金屬離子對脲酶的抑制作用是不可逆的，因此基於對脲酶抑制來檢測汞離子的傳感器在多次與抑制劑接觸后，很難使用再生溶液將脲酶的活性完全恢復，有必要研究一種可更新的脲酶傳感器。
  7. A research about decreasing in elbow flexor inhibition after cervical spine manipulation in patients with chronic neck pain

    頸脊柱推拿對減輕慢性頸痛患者肘屈肌抑制機制研究
  8. These nerves mediated the majority of inhibitory responses in the gi tract and regulate many important physiologicai reflexes, such as relaxation of the lower esophageal sphincter after swallowing, receptive relaxation of the proximal stomach during eating, and descending inhibition in response to distension

    這些nanc能神經介導大多數胃腸道運動的抑制性反應，參與許多重要的生理反射，如吞咽之後的食管下括約肌舒張、進食后胃體的容受性舒張、消化道的下行性抑制反應及胃腸蠕動等。
  9. The expression conditions of e2 gene in p. pastoris were optimized, the results indicated that the peak obtained after 72 hours ; pattern of inhibition / induction could improve expression level ; the best ph value were between 7. 5 and 8. 0 and the optimized methanol - induced concentration was 2 % - 3 % the e2 genes of the prevalent strain ( guangxi yulin strain ) and c strain derived from rabbit spleen tissue were amplified and cloned into e. coli the expression vector pproex - htb respectively, the recombinant plasmids pproex - gxyl and pproex - c were obtained and then were transformed into the dh5a e. coli competent bacteria respectively, the recombinant bacteria could express the major antigen region of e2 gene, the expression yields amount to 35 % and 38 % repectively

    豬瘟病毒ez基因的原核表達： pcr擴增出當前豬瘟流行野毒株，中國豬瘟兔化弱毒（ c株）兔脾組織毒ez基因的主要抗原區，將其克隆到原核大腸桿菌表達載體pproex htb中誘導表達，經sds page檢測表明，重組質粒能表達ez基因主要區蛋白， westernblot檢測表明，誘導表達蛋白與豬瘟陽性血清發生特異性反應，表達量為35和38 ，可用於基因工程診斷抗原。
  10. 2. the resistence of transformators were selected by g418 after co - culture with agrobactrium tumeflien, which was 40 mg / l in subcultured medium and 50mg / l in differeniated medium. in the process of killing agrobactrium, cef, amp or carb were also useful and the time of inhibition was long too

    經與農桿菌共培養后轉化子的鑒定選用g418 ，在繼代篩選培養基中添加40mg l ，在分化篩選培養基中添加50mg l ；在除菌過程中，頭孢噻肟鈉、羧芐青霉素、氨芐青霉素抑菌效果較好，抑菌時間較長。
  11. The protein level of p27 klpl increased at ih, decreased from 6 to 24h after 2gy, it decreased from 3 to 24 h after logy, and the level of p27kipl associated with cdk2 decreased, then lost its inhibition function to cyclin - dependent kinase

    Eycline / enkz的負調控因子p27k ， p 』蛋白表達水平在zoy照射后lh略有增加， 6一9h開始下降; 10gy照射后3h開始下降，持續到24h ，可見，隨著ir劑量的加大和處理時間的延長， p27kip 『蛋白表達水平下降的程度加大。
  12. The protein level of nf - kb in nucleus peaks at 6 h after stimulation and persists for at least 6 h. pdtc ( pyrrolidinedithiocarbamate ), an inhibitor of nf - kb, the effective concentration of it for nf - kb inhibition without any toxicity on cells is up to 100 umol / l, can significantly block no production induced by oligochitosan. although the study reported herein reveals that oligochitosan induces no production via nf - kb in macrophage, which is an important signaling mechanism of oligochitosan inducing immuno - enhancement of macrophage in vitro

    加入100林mol / l劑量的nf一忍抑制劑毗咯烷二硫代氨基甲酸鹽（ pnte ）作用於rawz 「 . 7細胞（ 4火10 ，個細胞/ ml ） 90rnin ，然後再加入100林留而劑量的殼寡糖對巨噬細胞進行刺激，發現pdtc在各個時間點（ 6 、 12 、 18 、 24h ）都明顯抑制殼寡糖對巨噬細胞no的誘導作用。
  13. ( 4 ) after surgery, evaluate the recovery of muscle relaxation and distinguish cause of breath inhibition

    （ 4 ）評定術后肌張力的恢復，區別術后呼吸抑制的原因。
  14. Inhibition of after catarat formation by all - trans retinoic acid

    全反式維甲酸對后發型白內障形成的抑制作用
  15. Study on inhibition of fesh - cut potato browning after treatment with several kinds of edible films

    幾種可食性膜對鮮切馬鈴薯褐變抑制的比較
  16. The positive transformants with the integrates mn - sod gene was identified by zeocin - resistance, pcr screening and expression in p. pastoris. the recombinant mn - sod protein was successfully expressed in pichia pastoris based on the evidences that a relative molecular weight about 23kd appeard in sds - page, the obvious activity of sod existed in native - page and enzymatic activity test, and mn - sod activity was specific base on the inhibition with the mixture of chloroform - enthanol ( 3 : 5 / v : v ) and potassium cyanide. two secreted plasmids ppiczaa - sodm18 and ppiczaa - sodc were constructed and after there linearization were transferred into chromosome of pichia pastoris gs115 by electroporation

    Pcr鑒定及mut表型分析進一步說明，目標基因已經重組到宿主菌基因組染色體上； 0 . 5甲醇誘導表達后， sds - page結果顯示，表達的蛋白相對分子量約為23kd ，活性電泳出現明顯活性條帶；酶活性測定顯示，重組菌株sod活性比對照提高5倍左右；氯仿-乙醇（ 3 : 5 v : v ）和kcn （ 5mmol l ）抑制反應進一步證明，所表達的sod為錳超氧化物歧化酶。
  17. In 200mol / l cisplatin, no telomerase inhibition was found when cells were collected only after 4 hours of drugs treatment, but the telomerase activity of cells was completely inhibited by cisplatin when removed the drug and recultured for 20 hours. however, vitamin c had no effect. in 8mol / l cisplatin, it was similar with 200mol / l cisplatin to uppress the telomerase acting of caov3

    Ddp對端粒酶活性的影向：當200mol lddp作用caov3細胞4小時，即刻收集細胞，藥物未對細胞端粒酶活性產生抑制；在細胞經過4小時ddp處理，去除藥物再培養20小時，端粒酶活性完全抑制； 8rmol lddp作用細胞24 j 』時，端粒酶活性部分抑制；當sumol lddp作用細胞120 j 』時，對端粒酶活性顯著抑制? 2 ?作用。
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