鏈端羧基 的英文怎麼說
中文拼音 [liànduānsuōjī]
鏈端羧基
英文
carboxyl terminal group-
Each fatty acid consists of a hydrocarbon chain with a carboxyl group at one end.
每個脂肪酸由一端帶有一個羧基的碳酸鏈組成。It is most efficient in clearing the peptide bonds on the c-terminal side of such amino acids tyrosine.
它對裂開諸如酪氨酸這類氨基酸的羧基末端的側肽鏈最為有效。In vivo, the two functional forms of rat mapllc3 with apparent mobilities of 18 and 16kda, termed lc3 - i and lc3 - ii, separately, were produced by a series of post - translational modifications including a characteristic c - terminal cleavage after the conserved glyl20 residue and this cleavage is essential for the membrane association of the 16kda rat map1lc3 protein.,
其中18kda的map1lc3蛋白是微管相關蛋白1的輕鏈亞基,稱為lc3 - ;另一種16kda的map1lc3蛋白則是自噬體膜的必須組分,稱為lc3 - 。 lc3 -和lc3 -都是一系列翻譯后修飾的產物,其中特徵性的修飾是在保守gly120后發生的羧基端切割,此切割修飾對lc3 -定位於自噬體膜尤為重要。The synthesis technology of various liquid rubbers with different active group terminated, such as hydroxyl - terminated, carboxyl - terminated, isocyanate - terminated, ami - no - terminated, mercaptan - terminated and various main chains like polybutadiene, polyurethane, polystyrene were reviewed with 23 references
摘要綜述了端羥基、端羧基、端異氰酸酯基、端氨基、端巰基等活性端基,以及聚丁二烯、聚氨酯、聚苯乙烯等不同主鏈結構的液體橡膠的合成技術。We wonder whether these conservative sites determine the tcrv specificity of sed, and whether sed and other ses share the same mode interacting with tcrv. it has been demonstrated that sed and sea have the same sites binding to mhc
有研究表明, sea具有兩個mhc結合位,氨基末端的結合位與mhc的鏈結合,羧基末端的結合位與mhc的鏈結合,阻止sea與mhc鏈結合可影響sea對某些tcrv ~ + t細胞的活化。As well as in eukaryocyte ( hepg2 and cos - 7 ), then detect their antigenity as a basis study and explore of the choice of immunogen for preventive and therapeutic vaccines of hepatitis b. methods : the gene fragments coding 152aa ( si ) and 124aa ( s2 ) of the carboxyl terminus of hbsag were amplified by pcr from plasmid pecob6 with a pair of primers containing different endonuclease sites and were cloned into multiple cloning sites of plasmid pbks ( + )
為乙型肝炎的預防和治療性疫苗免疫原的選擇進行初步的研究和探討。方法:本研究利用聚合酶鏈反應( pcr ) ,通過設計帶有不同酶切位點的一對引物,從質粒pecob6特異性擴增hbsag蛋白羧基末端152個氨基酸( s1 )和124個氨基酸( s2 )的基因片段,分別將二者克隆到質粒pbks ( + )的多克隆位點,篩選重組克隆。分享友人