The patterns of amyloplast proliferation behaved "amyloplast envelop dilating, evaginating, and budding to form new amyloplast","amyloplast envelop constricting to form new amyloplast","form new amyloplast as the middle clapboard" and "amyloplast envelope dilating and invaginating to form new amyloplast".

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The patterns of amyloplast proliferation behaved "amyloplast envelop dilating, evaginating, and budding to form new amyloplast","amyloplast envelop constricting to form new amyloplast","form new amyloplast as the middle clapboard" and "amyloplast envelope dilating and invigilating to form new amyloplast".

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The double membrane vesicle, which was produced by budding of the outer membrane of amyloplast, accumulated starch to form new amyloplast. The double membranes of amyloplast invaginated and the inner membrane dilated to form new amyloplast in the amyloplast.

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Under normal temperature.the Ca2+-ATPase activity was found on the innerside of the PM.on the vacuole envelope and the chloroplast envelope,and theenzyme activity declined upon heat stress.The Ca2+-ATPase activity on the vacuoleenvelope,PM.and the chloroplast envelope in both Ca2+-and oxalate-treated peppermesophyll cells was higher than that in the control under the same condition.TheCa2+-ATPase was also found at the granum lamella,and it was activatedsignificantly by exogenous Ca2+ and oxalate treatments.Under heat stress.the Ca2+-ATPase activity declined slowly in both Ca2+- and oxalate-treated mesophyll cells.But La3+ treatment inhibited the enzyme activity under both normal condition andheat stress.

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Protease treatment of the plasma membranes could abolish the binding but NaIO_4 and glycosidase could not, indicating that nsLTP144 bound to plasma membranes protein without carbohydrate moiety. Using the homobifunctional cross-linking regent bissuberate (BS~3) and rice plasma membranes incubated with ~(125)I-Trx-nsLTP144, we identified, after SDS-polyacrylamide gel electrophoresis and autoradiography, a putative protein receptor on the rice plasma membranes with the molecular mass around 60 kDa. NsLTP144 can not trigger extracelluar alkalization in arabidopsis, but can abolish the extracellular alkalization effect of phytopathogen elicitor cryptogein, suggesting that cryptogein and nsLTP144 may bind to the same membrane protein. In vitro pull-down assay showed that nsLTP144 interacted with OsCaM1, a possible extracellular calmodulin, implying that nsLTP144 and OsCaM1 could function in the same signal transduction pathway. These results shed light on revealing the roles of nsLTP in vivo and make it promising to finally characterize the plasma membranes receptor of nsLTP.

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Grew on the normal temperature, it was shown that the deposits of calcium antimonate being the indicator for Ca(superscript 2+) localization mainly concentrated within the vacuoles and intercellular spaces and there was also some Ca(superscript 2+) deposits in cell walls. But when Garyota urens L. was treated by the temperature of 2℃ for 48 h, the level of Ca(superscript 2+) increased in cytoplasm and plasma membrane, but decreased in vacuoles and intercellular spaces considerably. At the same time, the ultrastructure of chloroplasts suffered from chilling: the membrane of chloroplasts had been damaged, the layer of thylakoids was exiguous and unclear, the photosynthetic rate decreased evidently. And when Garyota urens L. was treated by the temperature of 2℃ for 120 h, the deposits of Ca(superscript 2+) mainly concentrated within the cytoplasm, nucleus and plasma membrane and there was also some Ca(superscript 2+) deposits in vacuoles, and the ultrastructure of some cells was simultaneously damaged severely: Chloroplasts structure, vacuole membrane and nuclear membrane had been damaged fully, the structure within the cell had become unclear, and the cell only have respiration.

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The micelle granules were accumulated in the guttate structure. Both liquid crystal phase and isotropic phase coexisted here. With the volatilization of solvent, the structures can change from disc or hexagon to cube with the variation of environment and interior reciprocity.

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The sex pheromone-producing gland of Ancylis.sativa Liu is amodified intersegmental membrane as a dorsal bag between eighth and ninthabdominal segments.

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The patterns of amyloplast proliferation behaved "amyloplast envelop dilating, evaginating, and budding to form new amyloplast","amyloplast envelop constricting to form new amyloplast","form new amyloplast as the middle clapboard" and "amyloplast envelope dilating and invaginating to form new amyloplast".

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We hypothesize that a transition from lysines to arginines such as that observed in tunicates (30), in conjunction with a loss of the core region, could have resulted in the differentiation of the arginine-rich protamines of the P type.

我們假定從離氨酸到 arginines 的一個(gè)轉(zhuǎn)變?nèi)绱说漠?dāng)做觀察在有被膜的(30)玖玖国产精品，連同核心區(qū)域的一個(gè)損失国产AV永久福利资源网站，可能造成 arginine 的區(qū)別-p 類型的富有 protamines。

basement membrane：基底膜

如透明角質(zhì)顆粒51久久综合狠狠综合久久综合、被膜顆粒、張力原纖維等. 這些成分中任何一種如有缺乏,均可影響角質(zhì)的形成. 由于角質(zhì)上層細(xì)胞間的橋粒逐漸消失,使它們能有規(guī)律的脫落,保持表皮的正常厚度. (六)基底膜 基底膜(Basement membrane)是真皮和表皮的交界,在

decapod：十足類/有十腳的

decapitator /斷頭器/ | decapod /十足類/有十腳的/ | decapsulation /無套模/被膜剝脫術(shù)/

polisher：拋光機(jī)

參加對象:可以很好的進(jìn)行汽車空軍1號車漆被膜操作,有過用拋光機(jī)(polisher)操作的經(jīng)驗(yàn). 因?yàn)檎莆掌嚳哲?號車漆被膜的基本操作是參加的基本條件之一,所以我們在培訓(xùn)前將對參加者的技術(shù)水平進(jìn)行確認(rèn).

tunica：膜

tungstyl /鎢氧基/ | tunica /膜/ | tunicate /有被膜的/有被囊的/

tunicate：有被膜的

tunic 束腰外衣 | tunicate 有被膜的 | tunicle 法衣

tunicate：有被囊的

有被膜的tunicate | 有被囊的tunicate | 有壁細(xì)胞lepocyte

tunicate：有被膜的/有被囊的

tunica /膜/ | tunicate /有被膜的/有被囊的/ | tunicle /法衣/

tunicle：法衣

tunicate 有被膜的 | tunicle 法衣 | tuning fork 音叉

mesorchium：睪丸系膜

睪丸被腹膜的褶襞所包裹,覆蓋其表面的部分形成生殖上皮,與腹腔壁連結(jié)的部分形成睪丸系膜(mesorchium). 在哺乳類生殖上皮的下面,有結(jié)實(shí)的結(jié)締組織的白膜(tunica albuginea),睪丸實(shí)體被睪丸小隔(sep-tula)分隔成許多小葉.

encapsulated ending：有被末梢

encapsulated 有膜的 | encapsulated ending 有被末梢 | encapsulated larva 被囊蚴