糖原粒 的英文怎麼說

中文拼音 [tángyuán]
糖原粒 英文
glycogen granule
  • : Ⅰ名詞1 [化學] (碳水化合物) sugar 2 (食糖的統稱) sugar 3 (糖果) sweets; candy; sweety Ⅱ形容...
  • : Ⅰ形容詞1 (最初的; 原來的) primary; original; former 2 (沒有加工的) unprocessed; raw Ⅱ動詞(原...
  • : Ⅰ名 (小圓珠形或小碎塊形物) small particles; grain; granule; pellet Ⅱ量詞(用於粒狀物)
  1. Following with the condensing of chromatin, nucle us gradually elongates and spires. a large number of vesicles turn into glycogen granules behind mitochondria. the mature typical sperm of cipangopaludina chinensis, having monoflagella, consists of a spiral head with only one spiral buddle conformed of nucleus, a spiral middle piece with four s

    中國圓田螺成熟典型精子單鞭毛,由頭、中、尾三段構成:頭段螺旋狀,旋束由細胞核構成,僅單股;中段也呈螺旋狀,旋束由線體構成,共四股;尾段非螺旋狀,主要由構成。
  2. Rich variety of natural climate, dry and rainless, irrigated by the melt water of tianshan mountain ' s ice and snow, sufficient sunlight, significant temperature gap between day and night, suitable for growth and cultivation of different types of wine grape, few disease and pest, high grape sugar contents level, moderate acid level, good color and luster, ideal material for producing top grade green food wine

    自然氣候類型多樣,乾旱少雨,天山冰雪融水灌溉,光照充足,晝夜溫差大,適宜酒葡萄不同品種的生長發育,病蟲害少,葡萄果量高,酸度適中、色澤好,是生產綠色食品高檔葡萄酒的理想料。
  3. The potato granules are manufactured through add - back process, and they have kept the original flavor and nutrition if potatoes as much as possibly, and are popular food in the world due to low fat and sugar

    本生產線是用馬鈴薯為料生產顆全粉,採用回填工藝生產出的顆全粉,最大限度地保持了馬鈴薯有的風味和營養價值,是一種低脂肪、低份的全球性食品。
  4. The typical sperm of cipangopaludina chinensis, having spiral nucleus, long and spiral mitochondrion and a large number of glycogen granules, belongs to the modified sperm

    中國圓田螺典型精子是一種修飾型精子,含有螺旋狀的細胞核,拉長並螺旋的線體和大量的物質。
  5. Extensive mitochondrial dna polymorphisms were found among lagurus lagurus, mus musculu , rattus norvegicus and mice. the findings will help us to understand the dispersion and evolution of these animals

    通過瓊脂凝膠電泳對這些片段進行測定,同時估算出草兔尾鼠線體dna的長度約為16 . 6kb 。
  6. The main pictures are as follows : distended rough endoplasmic retieula ; remarkably decreased number of rough endoplasmic relicula and degranulstion ; dilatated and vacuolized smooth endoplssmic reticola ; swollened nad deformed mitochondria ; destroyed structure of mitoehondria ; remarkable decrease in glycogenosomes, even disapparence of glycogenosomes

    主要表現為:粗面內質網擴張,數量明顯減少,並有脫顆現象;滑面內質網擴張呈空泡狀;線體腫脹、變形,結構遭到破壞;明顯減少,甚至消失。
  7. Abstract : we have investigated the ultrastructural changes of the biopsied muscle specimens from 8 cases of metabolic myopathies including 3 cases of glycogenosis, 2 cases of lipid storage myopathy and 3 cases of mitochondria myopathy. diagnosis and differential diagnosis with tem for metabolic myopathy as well as the significance of some ultrastructural changes were discussed in this study

    文摘:本文對3例累積病, 2例脂質沉積性肌病和3例線體肌病共8例代謝性肌病肌活檢標本的超微病理改變進行了觀察分析,對代謝性肌病的超微病理診斷、鑒別診斷以及某些病理改變的診斷意義進行了初步探討。
  8. And the field emission measurement was carried out at a pressure of 10 - 4pa. diamond powders coated with sliver are deposited on ito glass using electrophoresis coating method, through a solution of powders in isopropyl alcohol

    利用葡萄的還性將銀鹽中的銀還出來,在超聲的條件下,還出的銀將包覆在分散於溶液中的金剛石顆上。
  9. The cytoplasmic clearing is due to glycogen content which can be demonstrated by pas positiity

    瘤細胞較大,多邊形或圓形胞界清晰,胞漿透亮含、脂質或紅染顆, pas染色陽性反應。
  10. 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;快速復溫后植入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入12周后仍有肌腱細胞存活並分泌型膠;隨著時間延長, 10二甲基亞碸( dmso ) +棉子( 30mmol l ) + kh _ 2po _ 4 ( 25mmol l )組線體空泡減少,肌腱細胞排列整齊,膠纖維增粗並連接,抗拉強度增高。
  11. Second, a prokaryotic expression construct, obtained from invitrogen transformed into prokaryotic and induced to express vp1 protein. the expressed vp1 fusion protein was purified by affinity chromatography using glutathione - agarose resin and used in elisa and western bolt analysis as the antigen. the elisa and western blot results showed that the anti - fmdv antibody was elicited specifically against vp1 antigen

    第二,為了得到抗蛋白,將vp1的核表達質pgex - 4t - vp1轉化入大腸桿菌bl21中,經iptg誘導,裂解細胞後用瓊脂珠進行純化,用elisa和westernblot進行檢測,結果表明誘導表達出所需大小的融合蛋白。
  12. Cytochemical methods : the testis was fixed in cold acetone, embedded in paraffin, sectioned at 6 u m, observed with olympus bh - 2 microscopy and dna was showed with feulgen, glycogen was showed with pas

    細胞化學樣品以冷丙酮固定,常規石蠟包埋,切片厚度為6 m , feulgen反應顯示dna ; pas反應顯示, olympusbh - 2型顯微鏡觀察。
  13. Our ultrastructural observations provided more convincing evidence that the hepatic phenotype was induced. before the sodium butyrate treatment, the cells contained few organelles except some mitochondria and ribosome

    電鏡下觀察,胞漿中的細胞器較誘導前明顯增多,有線體、內質網和高爾基體以及大量的核體和
  14. Objective to prepare ea and ed protein of p - galactosidase with gst fusion protein by pgex - 4t - 2 expression system, and study its a complementation activity. to lay a good foundation for further study of cedia and utilization in expression immunoassay. methods an artificial synthesized dna segment coding for residues 6 - 56 ( modified ) of p - galactosidase ( ed protein ) was ligated to pgex - 4t - 2 vector

    實驗方法通過人工合成編碼d半乳昔酶ed蛋白的dna並插入核表達載體pgex 4t 2 ;從陀v p galactosldasecontrolvector質中用sal及earl進行雙酶切得到編碼卜半乳昔酶a一受體( ea )的大部分dna , n端再加上約60hp人工合成洲a ,連接后轉入pgex葉t億載體中。
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