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APC/C is activated at anaphase of mitosis,and engages in cell cycle regulation.

APC/C在细胞的有丝分裂期后期激活,调控细胞完成有丝分裂。

Cell plate A structure that appears in late anaphase in dividing plant cells and is involved in formation of a new cell wall at the telophase stage of mitosis .

细胞板:植物细胞分裂晚后期出现的一种结构,它和有丝分裂末期新细胞壁的形成有关。

The layer of gelatinous material that separates the inner and outer cell layers of a coelenterate.

胚盘由哺乳动物受精卵分裂而形成的细胞层。后期分裂为三层,胚胎由此发育

While under natural low temperature (10-20℃), a great deal of abnormalities, including micro nucleoli, scattered and lagged chromosomes and anaphase bridges were detected during PMC meiosis, even though the abnormalities were different between the two cultivars; the ratio of micro nucleoli was 22.88% of average, which was obviously higher than that of control (4.56% of average under normal temperature); and the ratios of univalent and multivalent in diplotene, which increased seriously, were 8.82% and 17.65% of Tainong 1, and 14.52% and 24.19% of Irwin under natural low temperatures.

低温(10~20℃)条件下,减数分裂过程中核仁的行为发生大量异常,微核仁的平均检出率高达22.88%,明显高于常温条件下的平均4.56%;双线期单价体和多价体的发生频率有明显增加,其中台农1号为8.82%和17.65%,Irwin为14.52%和24.19%;减数分裂中期Ⅰ、Ⅱ及后期Ⅰ、Ⅱ均观察到落后染色体,其中台农1号异常率为12.73%、5.63%、15.79%和4.76%,Irwin为11.11%、7.61%、9.52和6.38%。

SRG-L protein wasmainly observed in diplotene/pachytene spermatocytes, round and elongating spermatids.We can conclude this gene was activated during the early stage of meiosis, andtranscription of it kept high level during spermiogenesis.

因此初步判断这个基因在减数分裂早期被激活,转录在整个精子形成期维持较高水平的表达,有可能在精子发生后期起特殊作用,与减数分裂和精子变态成形相关。

In metaphase, Septin 1 is situated in equatorial plate. In anaphase, it is located in centrosome and in telophase, it is in post-mitosis bridge. The mutation of phosphorylation sites does not affect the location of Septin 1 itself and Aurora-B.

在有丝分裂中期位于赤道板,后期位于中间体及末期的后有丝分裂桥,磷酸化位点的突变没有影响自身和Aik2的定位。

During the mitosis, the correct separation of sister chromatids is necessary in normal transition from anaphase to telophase and it guarantees exact distribution of DNA. The non-disjuction is the important reason for forming the aneuploid.

在有丝分裂时,姐妹染色单体的正确分离既起到保证遗传物质准确分配的作用,又是分裂细胞从后期向末期过渡所必需的;而姐妹染色单体不分离则是产生非整倍体细胞的重要原因。

The results were as follows: 1.Inoculated on the induction medium at the late uninucleate stage,the microspores could initiate embryogenesis by first divisions in both symmetric and asymmetric patterns,but the former was predominant.

通过观察玉米小孢子胚胎发生的细胞形态学特征,发现:离体培养条件下单核后期的花粉可以通过均等分裂和不均等分裂两条途径形成胚状体,与前人的研究结果一致。

The reseach on activity changes of SOD, POD and CAT during the somatic embryogenesis of Y35 showed:(1) The activty of SOD was from 52.98 to 133.20 U·g-1·h-1, and remained a rising trend after early single embryo forming, this revealed that SOD might be positively correlated to the differentiation of embryogenic cell and the development of somatic embryo.(2) The activty of POD was from 0.05 to 0.50 U·mg-1·min-1, ascended firstly and desceded later, and was highest in embryogenic callus and lowest in late single embryo , this revealed that POD might be positively correlated to the division and differentiation of proembryo mass, while negatively correlated to the development of PEMⅢto late single embryo.(3) The activty of CAT was from 0.86 to 2.81 U·mg-1·min-1, showed an up-down-up trend, reaching to the highest peak at the time of early embryo formating and decreasing to the lowest at the time of early cotyledonary embryo formating, this revealed that CAT might be positively correlated to the development of early single embryo, while negatively correlated to the formation of middle single embryo and early cotyledonary embryo.The changes in activty of SOD, POD and CAT indicated these three antioxidant enzymes coregulated the differentiation and development of embryogenic cells during Larix somatic embryogenesis.4. Differentially expressed cDNA libraries of the stages of proembryo mass and somatic embryo maturation were successfully constructed by suppression subtractive hybridization.

对Y35体细胞胚胎发生过程中抗氧化酶活性变化的研究显示:(1)SOD活性在52.98~133.20 U·g-1·h-1之间,并在早期单胚形成后一直保持上升的趋势,表明其与胚性细胞的分化及体细胞胚的发育均具呈正相关;(2)POD活性在0.05~0.50 U·mg-1·min-1之间,呈现出先下降后升高的趋势,在胚性愈伤组织中最高,而在后期单胚形成时降至最低,表明其与原胚团的分裂和分化呈正相关,但与PEMⅢ向后期单胚的发育呈负相关;(3)CAT活性在0.86~2.81 U·mg-1·min-1之间,表现出升-降-升的变化趋势,在早期单胚形成时升至最高,在早期子叶胚形成时降至最低,表明其与早期单胚的发育呈正相关,而与中期单胚和早期子叶胚的发育呈负相关。

Our study includes four aspects. In the first aspect we study several important conditions of porcine oocytes maturation in vitro and oocytes cleavage after parthenogenetic activation and found mNCSU-23+15IU/mlPMSG+20IU/mlHCG+15% PFF+0.57mMcysteine is a good culture condition .When the Cocs are cultured in it ,the maturation rate and oocytes cleavage rate are higher than those of foreign covered. Our result are (86.7±3.35)% and (86.3±4.16)% and the highest report of foreign is(85.7±4.1)%.In the second aspect we study the effect of different chemical activations on development of porcine parthennogenetic embryo and found two best activation method. The first one is that putting the maturation MII oocytes in the 20μmol/L ionomycin for 30 minutes and then putting them in the NCSU-23 condition containing 5μg/mICB and 5mM/L6-DMAP for 3.5 hours, the oocytes cleavage rate and morulae/blastocysts development rate are (76.7±7.6)% and (37.1±6.4)%.The second one is that putting the maturation MII oocytes in the 200μM/L Thimerosal for 20 minutes and then putting them in the NCSU-23 condition containing 8mM DTT for 30 minutes

本研究分为4个部分,第一部分对影响猪卵母细胞体外成熟和孤雌激活后胚胎分裂的几个重要条件进行了比较研究,确立了一种较好的培养方法:与颗粒细胞共培养,找到了一种适合猪卵母细胞体外成熟的培养基:mNCSU-23+15IU/mlPMSG+20IU/mlHCG+15%PFF+0.57mM半胱氨酸,成熟率和分裂率分别为(86.7±3.35)%和(86.3±4.16)%,国外报道的最高成熟率为(85.7±4.1)%;第二部分对猪卵母细胞孤雌激活的化学方法进行了研究,确立了化学激活猪卵母细胞的两种最佳方法:1将成熟的去卵丘颗粒细胞的MII期卵母细胞用20μmol/Lionomycin作用30min,再将卵母细胞培养于含5μg/mlCB和5mM/L 6-DMAP(6-二甲基氨基嘌呤)的NCSU-23培养液中,卵裂率和桑囊胚发育率达到(76.7±7.6)%和(37.1±6.4)%2将成熟的去卵丘颗粒细胞的MII期卵母细胞在200μM/L的Thimerosal中处理20min,再与8mM的DTT共孵育30min,卵裂率和桑/囊胚形成率为(81.0±2.8)%和(39.6±2.7)%;第三部分对孤雌激活胚胎的培养条件进行了研究,确立了一种最佳的胚胎培养条件:在SOF简单培养基中添加颗粒细胞进行前3天的培养,然后转入添加胎牛血清的NCSU—23培养基并和输卵管上皮细胞进行后期的培养,其桑椹胚和囊胚的发育率为(59.5±3.2)%;第四部分研究了IGF-I

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