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- 引物DNA, DNA引物primed DNA
- DNA引物primed DNA
- 引物DNAprimed DNA
- DNA引物酶DNA primase
- 隨機引物DNA多態(tài)性Random amplification of polymorphic DNA
- 隨機引物DNA標記系統random primed DNA labeling system
- 隨機引物DNA合成標記系統random primed DNA labeling system
- 隨機引物DNA(合成)標記系統random primed DNA labeling system
- 端粒DNA序列在K~+、Na~+等離子的存在下能夠形成穩定的G4-DNA結構,這種結構阻礙了端粒酶對端粒DNA引物的識別,從而抑制了端粒酶的表達。The G-rich single-stranded telomeric DNA can adopt in vitro a variety of different non-B-DNA conformations such as an intramolecular quadruplex structure (G4-DNA).
- 因而，設計PCR引物時(shí)宜選擇Takahashi等分離株為標準。In China these viruses share high homology with Takahaski’s strains which might be good standards for primer designation.
- 錨定引物中擴增效果最好的是以CG或GC結尾的AP2、AP7。the most effective anchored primers were AP2 and AP7 ended by CGs or GCs .
- 同源引物差示PCR方法的建立及胎肝特異表達基因的差示篩選Development of Analogy Primer-mediated Differential Display-PCR and Identification of New Genes Differentially Expressed in Human Fetal Liver
- 采用兩對 P C R 引物檢測尿道及生殖道分泌物中的沙眼衣原體。Tw o pairs of P C R prim ers are used to test the chlam ydia trachom atis insecretion from urethra and vagina.
- 番茄RAPD分析有效引物3'端序列的偏倚分布及其與基因組序列結構的關(guān)系A Partial Distribution of the 3' Sequences of Effectual Primers in RAPD Analysis for Lycopersicon sp. And with Relation to Sequential Feature of Tomato Genome
- 根據基因庫己報道的人ICAM－2啟動(dòng)子和人CD59 intronl序列分別設計了兩對引物。According the reported sequence of human ICAM-2 promoter and DAF intron-1 in Gene Bank, designed two pairs of premiers respectively.
- 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.
- DNA測序引物sequencing primer
- (DNA)測序引物sequencing primer
- 引物原位DNA合成primed in situ DNA synthesis
- DNA復制引物順序DNA replication primer se-quence
