酶的亞單位 的英文怎麼說
中文拼音 [deyǎdānwèi]
酶的亞單位
英文
subunit of enzyme-
As indicated above, several m1gs that cleaved hcmv ul54 mrna segments in vitro were successfully designed and constructed. our studies demonstrates the utility of this ribozyme m1gs for antiviral application
我們的研究成功地利用引導序列，將核酶rnasep催化亞單位m1rna構建為序列識別的核酶m1gs ，證實了核酶在抗病毒方面的應用價值。Effects of arsenic trioxide on htert expression and tolemerase activity of human colonic carcinoma xenograft in nude mice
三氧化二砷對人結腸癌裸鼠移植瘤端粒酶活性及其催化亞單位表達的影響In our study we have cloned the osd gene from s. typhimurium by pcr, characterized the gene product and used this gene to construct asd + expression cloning vectors ptrc99a - asd
再將hpylori尿素酶b亞單位基因與尿素酶b和熱休克蛋白a融合基因分別克隆入ptrc99a一asd質粒的多克隆位點之內。Advance on catalytic subunit of telomerase in tumor
端粒酶催化亞單位在惡性腫瘤中的研究進展Reverse malignant phenotypes of colonic carcinoma cells transfected with antisense gene to htrt
反義人端粒酶催化亞單位基因轉染對人結腸癌細胞惡性表型的逆轉作用Expression of telomerase subunits in normal liver tissue and hepatocellular carcinoma tissue
肝細胞癌組織和正常肝組織中端粒酶亞單位的表達Methods : in cultured lung explants without serum, the lipid component synthesis of pulmonary surfactant was evaluated in [ 3h ] - choline incorporation ; mrna content of phosphocholine cytidylyltransferase ( cct ) in lung explants was investigated in rt - pcr ; the changes of the ultrastructure of the at ii cells were observed with electron microscope ; the expression of nmdar1 subtype was observed in immunohistochemistry staining ; nitric oxide synthase ( nos ) activity, nitric oxide ( no ) content, superoxide dismutase ( sod ) level, malondialdehyde ( mda ) content and lactae dehydroase ( ldh ) level were determined by biochemistry methods. results : 1. influence of glutamate on synthesis of the lipid component of pulmonary surfactant ? with l - arginine, glu inhibited [ 3h ] - choline incorporation with good dose - dependence and time - dependence ; ( 2 ) mrna content of cct of the glu treatment groups was decreased ; ( 3 ) glu increases the release of ldh in cultured lung explants ; ( dwith electron microscope histochemistry, glu induced the changes of the ultrastruture of at ii iv cells
方法：採用成年大鼠肺組織無血清培養，運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質磷脂酰膽堿（ pc ）合成量； rt - pcr擴增檢測肺組織中pc合成限速酶磷酸膽堿二胞苷酰基轉移酶（ cct ） mrna含量；透射電子顯微鏡法觀察肺泡型上皮細胞和ps系統超微結構的變化；免疫組織化學染色檢測glu的受體nmdar1亞單位的表達；生化測定肺組織乳酸脫氫酶（ ldh ）釋放量和肺組織勻漿中一氧化氮合酶（ nos ）活性、一氧化氮（ no ）生成量、超氧化物歧化酶（ sod ）水平以及丙二醛（ mda ）含量。Mpf ( m phase promoting factor ) which is made up of cdc2 as the active subunit and cyclin b as the regular subunit is a key factor in cell division. cdc2 is the active part of the mpf, which can active multiple ser / thr
Mpf （ mphasepromotingfactor ）是細胞分裂的中心調控因子，由催化亞基cdc2和調節亞基周期素b （ cyclinb ）組成，其中cdc2是mpf的活性單位，具有絲蘇氨酸蛋白激酶活性。Construction and identification of sense and antisense human telomerase catalytic subunit adenovirus expression vector
人端粒酶催化亞單位基因正反義腺病毒表達載體的構建及鑒定The ns1 and hns2 gene from aiv ( h9n2 ) isolate were cut from the pmd18 - t - nsl vector, the ns1 gene cloned into the sites of bamh i and xho i of prokaryotic expression vector and the hns2 cloned into the sites of ecor i and xho i of prokaryotic expression vector. the recombinant vector was identified by endonuclease
從含有禽流感病毒分離株非結構蛋白基因的重組質粒pmd18 - t - ns1中切取ns1 、 hns2基因片段，分別將其亞克隆于pgex - 6p - 1的bamh 、 xho位點和ecor 、 xho位點上，然後經單、雙酶切及質粒pcr鑒定，結果表明目的片段基因成功插入表達載體中。分享友人