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The results indicated that amyloplast was filled with starch mostly at 10 days after pollination. Amyloplast developed into mature starch granule at 15 days after pollination. Starch granule arranged tightly with protein body at maturation period.

结果表明:授粉后10 d,淀粉质体几乎完全被淀粉充满;授粉后15 d,淀粉质体已发育为成熟的淀粉粒,成熟期淀粉粒与蛋白质体排列紧密。

Water is filled into 1/3-2/3 of underground solution cave, and light type nuclear fusion body is put into the cave. Igniting the nuclear fusion body make water reach water vapour state in high temperature and high pressure 300-400 deg.C and 30-40Mpa, which drives rotation of turbo generator to generate electricity. With power being done, exhaust steam is condensed in condensator. Then, igniting the nuclear fusion body is carried out in another solution cave.

一种利用热核聚变能发电的方法,它包括以下步骤:在地下熔洞中注入占该熔洞1/3~2/3的水,并在该熔洞水中放入轻核聚变弹体,引爆该弹体后使熔洞中的水达到300~400℃、30~40Mpa的高温高压水蒸汽状态,并使之驱动汽轮发电机旋转发电,作功后的乏汽经冷凝器冷凝;在另一熔洞水中再引爆一轻核聚变弹体,使该熔洞中的水达到300~400℃、30~40Mpa的高温高压水蒸汽状态,并驱动汽轮发电机旋转发电。

Following 72 h co-culture, desquamate, sporozoites, trophozoites, meronts, microgametocytes, macrogametocytes, zygote, thin-wall oocyst, and thick-wall oocyst appeared orderly. Between the 60th and 72th hour, many oocysts emerged. Inoculated by the C. parvum -infected cell culture supernatant at the 48th hour, the immunosuppressed mice became infected.

在感染后72 h内,隐孢子虫出现连续发育阶段,包括脱囊、子孢子、裂殖子、裂殖体、滋养体、配子体、合子、薄壁卵囊和厚壁卵囊,在60~72 h内形成卵囊;用感染48 h的细胞培养上清接种于免疫抑制小鼠, 10 d后有隐孢子虫卵囊排出。

Both the new peniculus 1 and the old haplokinety separated at the telophase.The two germinal rows germinal rowsfor both the daughter cells appeared almost at the same time;(2) The macronucleus became shorter and thicker, finally oblate during the division of the cell. Then the macronucleus restored its original shape, band-like form. The micronucleus were divided into two before the macronucleus division;(3) The original scopula and stalk contributed to the old cell. The new cell formed scopula gradually after the cell division.

同时,新仔虫的第一咽膜(P′1)也开始由老单毛基索复制,并在细胞分裂后期与老结构分离;(2)大核在虫体分裂过程中由长带状逐渐缩短变粗至扁圆形,于虫体即将分开时迅速拉长,然后分裂为二个新大核;小核分裂先于大核,在两仔虫口纤毛器即将分开时完成;(3)原帚胚及柄归属老仔虫,新仔虫的帚胚在虫体分裂后逐渐形成,柄内肌丝则在柄鞘形成后逐渐长出。

The patients were recalled 6 months to 5years post operation. 8 cases healed with well face form,could masticate pap after denture restoration,without incision dehiscence or titaniumplate exposure. X -ray photographs showed no absorption of the transplanted bone, no image of lowdensity between titani-um plate and transplanted bone.

结果:钛板携带种植体植入下颌骨后切口一期愈合,6个月至5年随访,8例面部形态恢复良好,安装基台行义齿修复后可咀嚼软食,未见伤口裂开和钛板外露,X线拍片见种植体周围的植骨生存良好,植骨与种植体之间无低密度影

Second, the morphology of martensitic variant of each orientation turns from thin to thick oblate spheroid, which corresponds to the parallel motion of the yield surfaces for different orientations in subsequent yielding. But when grains of each orientation have turned into martensitic phase, the corresponding forward transformation plastic yield surfaces vanish and vice versa.

二是每个取向的马氏体变体形貌从薄的扁旋转椭球体到厚旋转椭球体的长厚过程,对应于每个取向的相变塑性屈服面在后继屈服中平行移动,但当该取向的晶粒全部转变为马氏体后,所对应的正向相变塑性屈服面消失,反之亦然。

And then adding NAA at low concentration in MS was used to give rise to roots. We also found that lower level of hormone could control effectively browninng and vitrifaction during the culture and G1 n (6mg/L) and AgNOj (2mg/L) supplemented in shoot induction media could improve the shoot information rates apparently (about90%).The whole period of plant regeneration from leaflets of peanut could be divided as five steps: germination - shoot induction -shoot elongation-rooting- tranplant.

用1/2MS培养基萌发花生种子,9-10d后,从无菌花生苗上切取幼嫩叶片中部为外植体。2500Lux光照和27±1℃条件下,在诱芽培养基(MS+BA3mg/L+NAA0.8mg/L+AgNO_32mg/L十Gln 6mg/L)培养12-14d即可观察到明显芽点或瘤状突起,较前人报道的培养时间大大缩短了,4w后芽点进一步发育成丛生芽,芽诱导率达90.2%,每个外植体平均产9个丛尘芽,然后转至培养基MS+BA3 mg/L+AgNO_32 mg/L上诱导芽的伸长,3-4w后可长至3-4cm,切下带有2-3片叶片的幼芽移至生根培养基(MS+NAA0.8mg/L+AgNO_32mg/L),1w后切口处可见白色不定根形成。

The allograft was harvested at 6h posttransplantation. Scrambled ODN group: The donor kidney was stored for 6h in ECs containing 1 u M Liposome/scrambled ODN complexes under hypothermal and hypoxia condition, then the donor kidney was transplanted into a SD recipient, and at 6h posttransplantation the allograft was harvested.

五、试验分四组:(1) Control组假手术组,Wister大鼠麻醉后,开腹后,即将伤口缝合,6h后切取左肾;(2) ECs组供肾经ECs(不含脂质体/ODN复合物)低温缺氧保存6h,移植到受体大鼠6h后切取移植肾;(3)deeoy onN组供肾经含1 pM的deeoy onN脂质体复合物的ECs 低温缺氧保存6h,移植到受体大鼠6h切取移植肾;(4)sc~。

According to the morphological characteristics of cementite lamellae, the deformed pearlite can be divided into three kinds: irregularly bent lamella (pearlite lamella originally inclined with large angles to the rolling plane and irregularly bent after deformation); coarse lamellae with shear-band (the rhomboidal blocks of weakly deformed lamella bounded by shear band) and fine lamella (heavily deformed lamella aligned parallel to the rolling direction with fine interlamellar spacing).

按渗碳体形态特点,变形珠光体组织可分为以下3种类型:(1)不规则弯曲片层型,即变形后的渗碳体与轧制面呈大角度偏离且不规则弯曲的珠光体。(2)带有剪切带的粗大片层型,即被渗碳体剪切带分开且变形轻微的珠光体。(3)精细片层型,即与轧制方向平行排列、片间距细小且渗碳体严重变形的珠光体。

He results show that the virus regained infectivity, and the tannins did not direct viricidal effect. Tannins extracted from Polygonum perfoliatum or Archontophoenix alexandrae seeds showed strongly anti-TMV activities separately. TMV virions seems to be aggregated when TMV incubated with the tannins by electron microscope. It seems that TMV coat protein bind to the tannins based on PAGE. Tannins did not reduce infectivity when applied either before or after TMV inoculation. It is proposed that tannins extracted from the 11 species inhibited TMV by binding with TMV coat protein to interfere with recognition site essential for viral coat protein. Tannins extracted from Euphorbia hirta, P. perfoliatum, P. cuspidatum reduce infectivity when applied immediately in N.

MV分别与这11种植物单宁混合后,通过透析除去单宁后,可恢复大部分侵染力,表明单宁对病毒粒体并无直接毒害作用;TMV与杠板归和假槟榔种子中提取的单宁分别混合后,电镜下观察粒体呈现明显的聚集现象;TMV外壳蛋白分别与这两种植物单宁混合后,聚丙烯酰胺凝胶电泳中CP泳带滞后;单宁在病毒接种前施用未降低TMV对叶片的侵染能力;这些结果表明植物单宁对TMV抑制作用可能是单宁与TMV-CP结合影响病毒对叶片侵染位点的识别而降低TMV侵染性,而这种结合是可逆的。

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The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了,排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意,我建议我们在价格上大家各让一半。

After an hour and no pup, look for continued contractions and arching of the back with no pup as a sign of trouble.

一个小时后,并没有任何的PUP ,寻找继续收缩和拱的背面没有任何的PUP作为一个注册的麻烦。