入胞分泌 的英文怎麼說

中文拼音 [bāofēn]
入胞分泌 英文
cytocrine secretion
  • : Ⅰ動詞1 (進來或進去) enter 2 (參加) join; be admitted into; become a member of 3 (合乎) conf...
  • : Ⅰ名詞1 (胞衣) afterbirth2 (同一個國家或民族的人) fellow countryman; compatriot Ⅱ形容詞(同胞...
  • : 分Ⅰ名詞1. (成分) component 2. (職責和權利的限度) what is within one's duty or rights Ⅱ同 「份」Ⅲ動詞[書面語] (料想) judge
  • : 泌名詞[書面語] (湧出的泉水) gushed spring water
  1. The proteins they make can enter the cisternae for transport to other parts of the cell or for secretion via the golgi apparatus

    此處產生的蛋白質可以直接進扁平囊進行修飾而後輸送到細的其他部位,或送到高爾基體進一步加工再被
  2. The cause that causes dark skiing ulcer has a lot of, have endocrine, food, genetic factor, the one mite bug that returning bug having mite also is the main reason that causes dark skiing ulcer lives inside wool bursa and sebaceous glands, it absorbs the nutrition of wool bursa and sebaceous glands cell, discrepancy skin carries a lot of bacteria, it secretes the dead damage body of excretive material and mite bug to be able to cause the skin organize inflammation to cause dark skiing ulcer

    引起暗瘡的原因有很多,有內、飲食、遺傳的因素,還有蟎蟲也是引起暗瘡的重要原因之一蟎蟲生活在毛囊和皮脂腺內,它吸收毛囊和皮脂腺細的營養,出皮膚帶很多細菌,它排泄的物質和蟎蟲的死亡殘體都會造成皮膚組織發炎引起暗瘡。
  3. Exocrine is the prostate cell secrete into little lobe

    由前列腺細小葉。
  4. Translocation from endocytic compartments to the cytosol is the essential and rate - limiting step in the intoxication process of most toxins such as ricin, diphtheria toxin, shiga toxin and pseudomonas exotoxin ( pe ). a number of these toxins are transported to trans - golgi network ( tgn ), and in many cases such transport to the tgn is required for the translocation and cytotoxicity. in deed, 5 % of the ricin endocytosed by cells has been shown to reach the tgn

    蓖麻毒素進的機理不甚明了,一般認為是rtb先與細膜受體結合,主要經過受體介導的內吞作用進吞噬體,然後沿著內體、高爾基體、內質網等逆向途徑,有序地運輸到內質網,最後從內質網轉位進漿,在漿內攻擊核糖體,從而抑制蛋白質的合成,導致細死亡。
  5. Rotating beams of light react with on photosensitive biological gel, which helps nutrition molecule penetrate into skin, strengthen circulation system, and stimulate hypothalamus to secrete hormone, enhance woman interior adjustment ability, channel ootheca, and stimulate the regeneration of cells, playing the function as health care

    利用旋轉光作用在光敏生物劑上,促進有效子滲體內,加強人體循環系統,刺激下丘腦,從而促進女性和荷爾蒙,增強女性機體調節能力,疏通卵巢部位淤滯,增強細再生,起到保健,調理的作用。
  6. The deleted mutant pap gene was also cloned into yeast secreted expression ppic9k vector to form ppic9k ~ 3, then the vector was transferred into pachia pastoris gs115 strain. the specific expression protein was secreted into the medium after inducing with methanol and the protein amount reached about 50 - 60 u g per millilitre measured by uv - absorbed methods in the supernatant of the medium via high density fermentation. sds - page results showed that there was one protein band in the gel which molecular weight was about 34ku

    將缺失型pap基因克隆于酵母型表達載體ppicgk構成重組載體,然後導畢赤酵母( p8chianastoris )菌株gslls細中,在甲醇的誘導下,經過酵母高密度發酵進行pap的表達,經sds page析,結果表明,在培養基上清液中含有一明顯的特異性蛋臼條帶,大小為34ku ,經western blotting析,該蛋白與法國pap抗血清有特異性反應,體外活性檢測表明該蛋白對tmv的侵染性具有高度的抑制性,說明該pap基因在畢赤酵母gs中也得到了正確表達。
  7. Note the epithelial cells lining the lumen demonstrate apocrine secretion with snouting, or cytoplasmic extrusions, into the lumen

    注意排成管腔的上皮細顯示了物進管腔的頂漿或細
  8. To get in vivo evidences that apoplast calmodulin con 1d regulate plant growth and development process, a chimeric secretion form of calmodulin binding peptide, which contains a signal peptide, a calmodulin binding domain and a c - myc epitope was constructed. the chimeric gene was introduced into arabidopsis. it was expected that the overexpression of this chimeric protein could be secreted into cell wall and bound to apoplast calmodulin, which could reduce the apoplast calmoduin concentration to make an apoplast camodulin " antisense " plant. by observing the potential phenotype change of apoplast calmodulin " antisense " plant, the in vivo function of apoplast calmodulin on plant growth and developmental process could be speculated

    但這些多是採用生理學手段和藥理學方法而得出的體外( invitro )實驗結果,為了取得質外體cam在植物生長發育過程中發揮重要作用的invivo實驗證據,根據動物中的一些研究方法,本實驗設計並構建了帶有信號肽、 cam結合肽( can小肽) 、 epitope ( c - myc )融合基因的載體,並將融合基因通過真空滲法轉擬南芥,預期過表達的融合蛋白將會被到細外並與質外體cam相結合,這樣就會抑制質外體cam的功能,從而可以構建質外體cam的「反義」植株,通過觀察質外體cam 「反義植株」的表型改變,就可以推斷質外體cam在植物生長發育過程中的功能。
  9. Morphological and endocrinological evidences have indicated that population of leydig ' s cells are not a homogeneity. present work focus on whether or not the heterogeneity of leydig cells has any relation with expression of star which is virtually important for understanding testis function

    形態學和內學研究表明:睪丸間質細並不是一個勻質的群體,間質細這種功能的異質性與star之間的關系是深理解睪丸功能所不可缺少的重要環節。
  10. The new synthesized protein was led to endoplastic reticulum cavity by eukaryotic secretory signal peptide sequence and then anchored to innerwall of endoplastic reticulum by kdel sequence, which interdicted the process of protein entering golgi body and cytoplasm, and then avoided heterogeneous glycosylation modification of foreign protein and prolonged the disappearance of half life of protein in organism. 2

    真核信號肽序列可以引導新合成的蛋白質進內質網腔, kdel序列將進內質網腔的蛋白質錨定在內質網內壁上,從而阻斷了蛋白質進高爾基體和細質的過程,進而避免了外源蛋白質的異源糖基化修飾,延長了蛋白質在生物體內的半衰期。
  11. Multicopy integrants were screened with g418 from pichia pastoris which contains recombinant plasmid, and induced with methanol to secrete interesting peptide. the supernate of pichia pastoris culture was analysed by sds - page and western blotting. a reactive band, which the apparent molecular weight is 36kd, can be detected with sheep anti - hcmv polyclonal antibodies

    重組質粒轉化巴氏畢赤酵母, g418篩選出多拷貝插的單克隆,甲醇誘導多拷貝插的單克隆酵母細目的蛋白,培養液上清經sds - page電泳析,在蛋白質印跡中檢測到培養液上清有一表觀子量為36kd ,能與羊抗hcmv多克隆抗體發生發應的條帶。
  12. The research team of prof chan hsiao chang, director of the epithelial cell biology research centre, in collaboration with zhejiang academy of medical sciences, demonstrated that cystic fibrosis transmembrane conductance regulator cftr is involved in transporting bicarbonate into sperm, and thus, is vital to sperm fertilizing capacity and male fertility. cftr is an anion channel, mutations of which cause cystic fibrosis, a disease characterized by defective cl - and hco3 - transport with clinical manifestations in a number of organ systems

    由陳小章教授領導的香港中文大學上皮細生物學研究中心的研究人員,與浙江醫學科學院合作,證實囊性纖維化跨膜電導調節器( cftr )負責輸送碳酸氫根進精子,對精子授精能力及男性生育能力非常重要; cftr是一個陰離子通道,其基因突變會導致囊性纖維化,因為氯離子和碳酸氫根( hco3 - )缺陷,引發一系列器官病徵。
  13. After the induction of iptg, the extracellular proteins of pet22asg / bl21 ( de3 ) plyss showed blue when treated with gus staining solution ; but the extracellular proteins of ck : bl21 ( de3 ) plyss showed no color change with the same treat. these results verified the function of secreting protein by grb - ast signal peptide

    將表達載體pet22asg導表達宿主菌e . colibl21 ( de3 ) plyss ,經iptg誘導表達,其外蛋白以gus染色液處理顯藍色;而對照空宿主菌bl21 ( de3 ) plyss誘導表達后,經同樣的處理,顏色無明顯變化,這初步證實了ast信號肽具有一定的蛋白的功能。
  14. The researchers also spliced a gene into the virus that makes it produce granulocyte - macrophage colony - stimulating factor, which induces the body ' s immune system to recognize and attack tumors infected by the virus

    研究人員還向病毒中插了一段基因使得受侵細粒細集落刺激因子,這促進了機體的免疫系統識別和攻擊受到病毒感染的腫瘤細
  15. In the present study, the express library of monoclonal anti - sp18 scfv ( single chain fragment variable ) gene is constructed and selected for further study of sp18 antigen on mammalian fertilization and embryogenesis. total rna were firstly isolated from these growing hybridoma cells which secretes monoclonal anti - sp18 antibodies. after obtained using rpas system, vh and vl genes were used to assemble scfv gene fragment with a linker primer

    應用重組噬菌體抗體庫技術,從小鼠抗牛精子sp18抗體的雜交瘤細系中離總rna ,克隆抗體重鏈和輕鏈可變區基因,加連接肽引物( linkerprimer )組裝成單鏈抗體scfv ( singlechainfragmentvariable )基因並用rs引物進行擴增, sfi 、 not酶切,回收后與pcantab5e載體相連,轉化e . colitg1宿主菌,構建單鏈抗體文庫。
  16. Methods the 54th generation of transformed human embryonic tendon cells and artificial composite materials of carbon fibers ( cf ) and polyglycolic ( pga ) were co - cultured in vitro to construct tet. lt was frozen in liquid nitrogen with four kinds of cpa for 2 months. post - thawed quickly and transplanted into hind limbs of nude mice, and repaired the defects of achilles tendon. after 2, 4, 6, 8, 12 weeks, the morphological, histological, ultrastructure, short tandem repeat loci and immunohistochemistry examination were detected, and biomechanical strength of tet were examined. result tendon cell survived and could secret type i collagen after 12 weeks to transplanted into nude mice. in the group of dmso + raffmose + kh2o4, vacuole in mitochondrion degraded i tendon cell ranged in order, abundant collagen fibers were found and linked each other and the biomechanical strength was increased as time elapsed. c onclusion dmso + raffmose + kh2o4 could protect tet in deep low temperature

    組織工程肌腱制備完成後在四種抗凍劑保護下液氮凍存2月;快速復溫后植裸鼠以修復跟腱缺損, 2 、 4 、 6 、 8 、 12周后取出,觀察形態學、組織學、電鏡和免疫組織化學變化,短串聯重復位點檢測和生物力學變化。結果實驗組組織工程肌腱體內植12周后仍有肌腱細存活並型膠原;隨著時間延長, 10二甲基亞碸( dmso ) +棉子糖( 30mmol l ) + kh _ 2po _ 4 ( 25mmol l )組線粒體空泡減少,肌腱細排列整齊,膠原纖維增粗並連接,抗拉強度增高。
  17. Signal recognition particle ( srp ) - - a particle composed of proteins and 7sl rna that binds to signal sequences and targets polypeptide chains to the endoplasmic reticulum

    訊息(指揮)序列- -蛋白質末端的一段疏水性氨基酸,在細菌中引導蛋白質或在真核細中將蛋白質併內質網。
  18. Signal ( leaser ) sequence a hydrophobic sequence at the amino terminus of a polypeptide chain that targets it for secretion in bacterial or incorporation into the endoplasmic reticulum in eukaryotic cells

    訊息(指揮)序列蛋白質末端的一段疏水性氨基酸,在細菌中引導蛋白質或在真核細中將蛋白質併內質網。
  19. It acts as a mediator molecule for adhesion between the surface of blastocyst and epithelial cell, and maybe involved in implantation regulation, mmp - 9 is highly expressed and secreted by trophoblast cells, and the antibody of mmp - 9 can inhibit the invasion of the trophoblast this indicates mmp - 9 is very important to the invasive embryo

    Mmp - 9 (基質金屬蛋白酶- 9 )在植過程中滋養層細大量和表達,而多克隆抗mmp - 9抗體可以阻斷這些滋養層細對基質的浸潤,這說明, mmp - 9對于胚胎的侵至關重要。
  20. The recombinant pcr technic was used to introduce a linking peptide klgggg to the site between scfv single chain form of the monoclonal antibody sz - 51 specific for the glycoprotein gmp140 on activated platelet membrane and uk32 low molecular weight form of pro - urokinase, to make the scfv - linker - uk32 chimeric gene. this gene was cloned into the transfer vector pbacpak9, and cotransfected with bacpak6 bsu36i digest into sf 9 cells. the fusion protein was secreted into the medium. in the fifth day after the cotransfection, the supernatant of the medium showed 107 iu ml fibrinolytic activity, higher than 25 iu ml fibrinolytic activity of scfv - uk32. elisa showed that the supernatant had the binding activity to activated platelet. wastern blotting also indicated that the supernatant could bind to the monoclonal antibody of urokinase b chain

    為了提高重組導向溶栓子scfv - uk32的溶纖活性,通過重組pcr方法在編碼scfv與uk32的堿基之間引編碼klgggg連接肽的堿基序列,並克隆到轉移載體pbacpak9上,通過與線性病毒dna bacpak6 bsu36i digest共轉染到昆蟲細sf 9內,進行表達。表達產物到上清中,共轉染后第5d天用纖維平板法測得sf 9細上清溶纖活性達到107 iu ml ,比未引連接肽的scfv - uk32的表達活性25 iu ml高。
分享友人