1)  RACE
RACE
1.
Cloning of variable region and signal peptide genes of anti-CD20 monoclonal antibody by RLM-RACE;
用RLM-RACE法克隆抗CD20单克隆抗体可变区基因及其信号肽基因
2.
The RACE amplifying and sequenceanalysing of hepatocarcinoma highly expressed gene P02;
肝细胞癌高表达基因片段P02的全长RACE扩增和序列分析
3.
Cloning of a Pathogenesis-related Protein Gene cDNA of Potato Using RACE Methods Combined with cDNA Library;
cDNA文库与RACE方法结合克隆一个马铃薯病程相关蛋白基因cDNA(英文)
2)  RACE
cDNA末端快速扩增
1.
METHODS: The full-length cDNA of rabbit BK_Ca beta subunit gene was amplified by 3′ RACE, 5′ RACE and RT-PCR from rabbit sphincter of Oddi (SO).
方法:采用3′及5′cDNA末端快速扩增(RACE)及RT-PCR技术从兔Oddi括约肌(SO)组织获得BKCa通道β亚基的全长cDNA序列。
2.
To find a novel gene which is related to protein of bovine seminal plasma (BSP) in human and study the new gene′s structural feature,expression and location in chromosome,the cDNA was cloned by using the 3′ rapid amplification of cDNA ends (RACE) and 5′ RACE methods and cloned into the expression vector of GST fusion protein (PGEX-5X-1),finally expressed in E.
采用cDNA末端快速扩增 (RACE)技术 ,克隆了一个BSP蛋白相关基因的cDNA序列 。
3.
Special primers were designed based on the sequence information of ferritin genes reported in the literature and used for rapid amplification of cDNA ends(RACE) for cloning Phascoloma esculenta ferritin gene.
根据已报道的铁结合蛋白基因的保守序列设计引物,用cDNA末端快速扩增(RACE)法,成功地从可口革囊星虫体液中获得铁结合蛋白基因的全长序列。
3)  RACE
cDNA末端快速扩增技术
1.
To understand the mechanism of chick focal adhesion kinase gene(FAK)expression and regulation,the transcription start sites and four kinds alternatively spliced 5′end(5′untranslated region,5′UTR)of FAK mRNA in chick embryo fibroblast cells were identified by RACE.
为了研究鸡局部黏着斑激酶(FAK)基因表达调控的分子机制,运用cDNA末端快速扩增技术确定了鸡胚成纤维细胞FAK基因的转录起始位点,并发现FAK基因mRNA的5′非翻译区(5′UTR)存在4种剪切形式。
2.
Rapid amplification of cDNA ends (RACE) is a polymerase chain reaction (PCR)-based technique which was developed to facilitate the cloning of full-length cDNA 5 and 3 ends after a partial cDNA sequence has been obrained by other methods.
cDNA末端快速扩增技术是一种基于多聚酶链式反应的技术 ,它的发展大大便利了应用其它方法获得的部分cDNA序列后克隆全长cDNA 5’和 3’末端的工作。
4)  RACE
cDNA末端快速扩增法
1.
notoginseng,was amplified by RACE strategy with the total RNA of root as the template.
方法采用cDNA末端快速扩增法,以三七根总RNA为模板扩增出三七FPS基因。
5)  RACE
快速cDNA末端扩增
1.
The rapid amplification of cDNA ends(RACE)technique and the electronic cDNA library select mathod was applied to amplify full length of the expressing sequence tag(EST) ,which is a specfic-stage in Schistosoma japonicum adult worm, and a cDNA fragment with an ORF was identified(GenBank accession number is AY847290).
利用快速cDNA末端扩增(RACE)技术结合“电子cDNA文库”筛选法,对日本血吸虫成虫期特异表达基因EST片段的全长序列进行了扩增,获得了一含完整开放性阅读框(ORF)的基因序列(GenBank中的登录号为AY847290)。
6)  RACE
cDNA末端扩增
1.
Gene specific primers derived from this partial sequence were used for the amplification of the 3′- and 5′-ends of this cDNA by RACE method,and this lead to a full-length cDNA sequence of 1 482 bp was amplified.
根据真菌Δ6 脂肪酸脱氢酶保守的氨基酸序列设计简并引物进行RT PCR ,获得一个 5 93bp的cDNA片段 ,再根据获得的部分序列设计基因特异性引物 ,通过cDNA末端扩增技术 (RACE)获得该cDNA的 3′和 5′序列 ,从而得到全长为 14 82bp的cDNA序列。
参考词条
补充资料:2-isopropyl-5-methyl-cyclohexan-1-on racemic
CAS: 1074-95-9
分子式: C10H18O
中文名称: 反-DL-5-甲基-2-(1-甲基乙基)环己酮

英文名称: 5-methyl-2-(1-methylethyl)-, trans-(+-)-Cyclohexanone;dl-p-menthan-3-on;2-isopropyl-5-methyl-cyclohexan-1-on racemic;trans-(+/-)-cyclohexanon;menthone racemic;p-menthan-3-one racemic
说明:补充资料仅用于学习参考,请勿用于其它任何用途。