戊細胞 的英文怎麼說
中文拼音 [wùxìbāo]
戊細胞
英文
epsilon cell-
Other isoprenoids are excreted into the extracellular space.
其他類異戊二稀則分泌到細胞外間隙中。Gfp - oscam61 was transported into the nucleoplasm upon a block in isoprenoid biosynthesis by mevinolin treatment of tobacco cells. these results indicate that the prenylated oscam61 molecules are mainly membrane - associated while its unprenylated counterparts are transported into the nucleoplasm. thus, oscam61 may play functions in coordinating ca2 + signaling with isoprenoid metabolism
用抑制異戊烯合成途徑的mevinolin處理轉化了gfp - oscam61的煙草細胞,原來定位於膜上的gfp - oscam61則進入細胞核,說明異戊烯化的oscam61結合在膜上而它的非異戊烯化形式存在於細胞核質中,因此, oscam61同時受鈣信號和異戊烯代謝的調控,並可能在鈣信號傳遞和異戊烯代謝的協調過程中發揮功能。If the skin has been put into 4 percent glutaraldehyde for three minutes or more. we are no longer able to get rid of the cells in it. the a - gal in porcine skin as disapered in acellular matrix treated by trypsin, dispase and sds
實驗發現4戊二醛對基質交聯固定后,若交聯時間短,則與不交聯組無差異,時間稍長,則胰酶無法脫除細胞。An unusual rice calmodulin isoform, oscam61, was first obtained in our lab, which contains an n - terminal cam domain and a c - terminal basic extension with a potential prenylation site. in vitro activity assays confirm oscam61 as a functional calmodulin. using the green fluorescent protein ( gfp ) as a visual marker, we further studied subcellular localization of oscam61 in stably transformed tobacco cells
利用綠色熒光蛋白( greenfluorescentprotein , gfp )作為標記,研究了oscam61在煙草細胞中的定位, gfp - oscam61融合蛋白(具有開放的異戊烯化修飾位點)定位於細胞質膜和細胞器膜上,而oscam61 - gfp (異戊烯化修飾位點被gfp封閉)定位於細胞核的核質中。The hnadcs ( human na + / dicarboxylate cotransporter 3 ) mediates the transport of krebs cycle intermediates, such as succinate, citrate and a - ketoglutarate, across the plasma membrane of many epithelial cells
人鈉二羧酸協同轉運蛋白3 ( humanna ~ + dicarboxylatecotransporter3 , hnadc3 )基因的編碼產物是位於多種上皮細胞膜表面的一類介導琥珀酸、枸櫞酸及-酮戊二酸等三羧酸循環中間產物轉運的蛋白。Leukemic cells killed by photodynamic therapy with 5 - aminolevulinic acid : an experimental study
氨基酮戊酸光動力學療法殺傷白血病細胞的實驗研究An acellular dermal matrix was prepared from allogenic skin by removing epidermis with a hyperosmotic salt solution and cross - linking with glutaralaldehyde, then clear away acellular components in dermis with naoh - maceration. the light and sme observation of the acellular dermal matrix revealed that the epidermis and cellular component in dermis were eliminated
本研究共分四部分:第一部分無細胞真皮基質的制備用高滲鹽除去異體皮膚的表皮細胞,經戊二醛交聯后以低濃度naoh消蝕以除去真皮中的所有細胞成分,得到無細胞真皮基質。The cell - matrix complex was incubated with dmem and 10 % bovine serum under condition of 37, 5 % co2 - the medium was changed daily. ( 3 ) cell - matrix complex paraffin section was made after 7 days incubation
將細胞懸液接種于戊二醛交聯的膠原一殼聚糖多孔膜,加dmem 10小牛血清培養基後放置37 』 c , 5 co 。Drug - induced pulmonary eosinophilia was suspected and valproic acid was discontinued
因為可疑為藥物引起的肺嗜酸細胞增多癥,丙戊酸被停用。The synthesis of poly ( - hydroxybutyrate - co - - hydroxyvalerate ) by the strain g - iiiy from different precusor was studied. it was found that the strain g - iiiy could accumulate phbv with sucrose as carbon source and propionic acid or valeric acid as precursor. in 2l self - controlled fermentor, the dry cell weight, phbv concentration and phbv content reached 35. 8g ? l - 1, 22. 6g ? l - 1 and 38. 4 % respectively in the case of fermentation for 42 hours and the propionic acid as precursor
研究了添加不同前體物, g - y菌株生產聚-羥基丁酸和聚-羥基戊酸共聚物( phbv )的發酵條件,結果表明,此菌株能以丙酸或戊酸為前體,在蔗糖為碳源的條件下合成phbv共聚物;在2l發酵罐中,以丙酸為前體,發酵16小時開始流加丙酸,根據發酵液ph值變化控制丙酸流加量,發酵42小時,細胞干重、 phbv產量和含量分別達到35 . 8g / l , 22 . 6g / l , 63 . 13 。Parthenogenetic activation and development of kunming mouse oocytes in vivo with pentobarbital sodium
昆明鼠體內卵母細胞的戊巴比妥鈉激活和發育Effects of penehyclidine hydrochloride on chinese hamster lung cells chromosome aberration in vitro
鹽酸戊乙奎醚對中國倉鼠肺細胞體外染色體畸變的影響The optimum conditions of the extraction of cucumber dna using sds method were as following ( for 1. 0 g cucumber ) : 4. 0 ml of cell extraction solution, 1. 0 ml of saturated kc1 solution, the rate between the phenol / chloroform / isoamyl alcohol solution, chloroform / isoamyl alcohol solution or isopropanol and the sample solution being 0. 6, 0. 6, and 0. 58, respectively
優化了用sds法提取黃瓜dna的條件。用4 . 0ml細胞提取液、 0 . 6倍樣液體積的酚氯仿異戊醇、 0 . 6倍樣液體積的氯仿異戊醇、 0 . 58倍樣液體積的異丙醇及1 . 0ml飽和kcl溶液,可從每克黃瓜中提取350mgdna 。分享友人