您要查找的是不是:
- DNA測序的通用引物universal primer
- (DNA測序的)通用引物universal primer
- 利用ITS的通用引物(ITS5-ITS4)對云南的美味牛肝菌(Boletusedulis)子實(shí)體的DNA進(jìn)行PCR擴增,擴增產(chǎn)物回收后直接測序。A pair of general primer (ITS5-ITS4) was used to test in amplification of internal transcribed spacer (ITS) region of chromosomal DNA of fruiting bodies of Boletus edulis in Yunnan.
- DNA測序引物sequencing primer
- 在SR1基因兩端設計引物,對綏農10號基因組進(jìn)行了擴增,經(jīng)測序獲得3972bp的DNA序列SR2。The gene has been submitted to the GenBank database, and the accession number is AY193892.3 Designed specific primers according to the sequence of SR1, a PCR reaction was done with the genome DNA of Suinong10 as template.
- 應用ABI PRISM~(TM)310測序儀進(jìn)行快速且經(jīng)濟的DNA測序Rapid and Economic DNA Sequencing Using ABI PRISM~(TM) 310 Sequencer
- 開(kāi)發(fā)Unicode是為了創(chuàng )建能容納多數已知腳本的通用字符集。Unicode was developed to create a universal character set that can accommodate most known scripts.
- 通用引物universal primer
- 綜合介紹DNA測序中常用毛細管凝膠電泳 (CGE)分離技術(shù)。The CGE separation technique usually used in DNA Sequence Determination is introduced in detail in this paper.
- 真菌特異性通用引物的聚合酶鏈反應系統的實(shí)驗與臨床研究Experimental and Clinical Study on Detection of Medically Import ant Fungi by PCR with A Universal Fungus-specific Primer System
- DNA測序、篩選cDNA文庫的加減法plus-minus method
- 啤酒污染乳酸菌PCR引物的設計The PCR Primers Design Of Beer Spoilage Lactic Acid Bacteria
- 方法:用血清學(xué)血型方法、PCR-SSP法和ABO基因第6及第7外顯子直接測序的方法對B(A)血型和B(A)型等位基因進(jìn)行檢測。Methods:ABO blood groups were identified by serological tests. B(A) alleles were determined by PCR-SSP and direct DNA sequencing at exons 6 and 7 of ABO gene.
- 方法用1、2、3類(lèi)三種整合酶基因通用引物擴增184株中段尿中分離革蘭陰性桿菌的相應基因;Methods To amplify the class1,2 and 3 integrase genes in 184 gram negative bacilli from medistream urine by polymerase chain reaction with universal primer of 3 genes.
- 成功擴增出HBeBP4A基因,測序結果符合GenBank報告序列。HBeBP4A gene was successfully amplified and identified by DNA sequencing.
- 例如,在過(guò)去的兩年中人們已經(jīng)借助于MGR和GRIMM軟件得到了大鼠與人以及最近新測序的挪威鼠之間的幾個(gè)比較有趣的進(jìn)化方案。For example, in the last two years, several very interesting evolution scenarios have been proposed between the mouse and the human, and between the mouse and the newly sequenced Norway rat, using the MGR and GRIMM software.
- 皺紋盤(pán)鮑(Haliotis discus hannai)微衛星DNA的篩選與引物設計Isolation and Primer Designing of Microsatellite Marker in the Pacifi Abalone(Haliotis discus hannai)
- 方法根據GenBank S.suis2epf基因序列設計引物,克隆ZYH24株epf基因片段并進(jìn)行序列分析;Methods:The epf gene fragment was amplified by PCR from ZYH24 and cloned into prokaryotic expression plasmid pGEX4T-2 to form pGEX4T-2-epf.
- 方法利用酶切及SSCP技術(shù)檢測凝固酶基因序列改變情況,并測序進(jìn)行確證。Methods DNA sequences of the coagulase were examined by polymerase chain reaction-sigle strand conformation polymorphism (PCR-SSCP) method and were identified by sequencing.
- 方法:應用RT-PCR結合測序方法研究白血病細胞系K562和CEM/VLB100APAF-1cDNA類(lèi)型;Methods:APAF-1 cDNA types in leukemic cell lines K562 and CEM/VLB100 were studied by cDNA cloning strategy.