通过pcr产物的酶切证实多态性情况。
Polymorphisms was identified by restriction analysis of PCR products.
通过酶切、PCR及测序鉴定各重组体。
The recombinants were analyzed and identified by restriction enzyme, PCR and sequencing.
用酶切和PCR的方法对重组质粒进行鉴定。
Used restrict enzyme and PCR to verify the reconstructed plasmid.
对胞壁质酶R2基因进行了限制酶切图谱分析。
The restriction map of R2 gene was construed for further use.
方法：采用DNA测序及限制性酶切反应方法。
Methods:DNA sequencing and restriction endonuclease reaction was used.
最后用限制性内切酶单酶切及琼脂凝胶电泳进行鉴定。
Finally, we could evaluate plasmids cDNA extracted with mono-restriction endonuclease enzyme and the AGAR gel electrophoresis.
同时对其纯度、浓度、分子量及酶切图谱进行了鉴定和分析。
Meanwhile, we also studied its purity, molecular weight, concentration and restrictive enzymatic map.
重组质粒经酶切和测序证实正确，然后转化大肠杆菌BL21。
The recombinant plasmid was confirmed by digestion and sequence, then transformed into E. coli BL21.
本研究利用多种组合的酶切分析，绘制了较为详细的酶切图谱。
In this study, a detailed restriction map was constructed using multiple groups of restriction endonuclease analysis.
经pcr鉴定、酶切鉴定和测序说明所克隆的两种基因是正确的。
Both genes were correctly cloned and identified by PCR, restriction enzyme digestion and sequencing.
酶切产物经3％琼脂糖凝胶电泳分离后，紫外灯下检测酶切结果。
Restricted DNA products were then separated by useng 3% agarose gel electrophoresis and visuslized by UV light.
结果酶切和测序证实PTEN基因克隆和真核表达载体构建成功。
Results Restriction enzyme analysis and DNA sequence analysis showed that PTEN gene was cloned and the eukaryotic expression vector was constructed successfully.
结果酶切及测序显示对OSCP基因有义突变部分的纠正获得成功。
Result Restriction endonuclease digestion and sequencing showed that the modification of the sense mutation of OSCP gene can be successful.
结果经酶切和DNA测序证明LIF基因序列正确，载体构建成功。
Results: LIF gene sequence and vector were verified correctly by enzyme digestion, sequence analysis.
用8%非变性聚丙烯酰胺凝胶电泳将酶切产物分离，并用银染法显色。
The products of endonuclease digestion were run on 8% non-denaturing polyacrylamide gel electrophoresis and detected by silver staining.
并对氨苄筛选的重组入外源基因的质粒通过P CR、酶切和测序鉴定。
Ampicilin - resistant transformants were selected and identified by PCR, Enzyme digestion and DNA sequencing analysis.
外源基因在细胞内的酶切保护问题是影响基因转染成败的重要因素之一。
Protection of exogenous genes against intracellular conditions is one of key factors in gene transfection.
结果：经PCR，酶切及测序方法鉴定，该腺病毒-整合酶嵌合系统构建成功。
Results:After being identified by PCR, restriction enzyme digestion and sequencing, the adeno-integrase hybrid system was successfully constructed.
建立和优化了大麦dna单限制性酶切选择性扩增多态性技术体系(SADF)。
A method named selective amplification DNA fragments (SADF) using single restrictive enzyme was established and optimized in barley.
结果经酶切和测序鉴定表明所构建的重组表达质粒中含有TSO45 - 4b基因。
Results: the constructed recombinant plasmid contained the sequence of TSO45-4B gene that was identified by endonuclease digestion and sequence analysis.
结果酶切鉴定和DNA测序分析显示，TROP2靶向RNA干扰重组质粒构建成功。
Results Enzyme digestion analysis and DNA sequencing showed that TROP2 targeted RNA interference recombinant plasmids were constructed successfully.
结论：经酶切鉴定构建的人透明带蛋白3重组表达载体可高效表达重组人zp3蛋白。
Conclusion The recombinant expression plasmid constructed by restriction enzyme cleave identification can highly express recombinant human ZP3 protein.
这暗示着卵母细胞成熟抑制因子靠酶切hax -1蛋白来启动线粒体中的细胞凋亡。
This suggests that Omi can initiate apoptosis in the mitochondria by cleaving HAX-1 protein.
PCR检测和酶切鉴定结果表明，在水平测试的混合饲料粉中可检出牛源、羊源性成分。
The bovine, sheep and goat derived materials were positive in mixed feed powders of level test by PCR and restriction enzyme analysis.
酶切加工产生的各种功能蛋白在病毒基因的复制、翻译、加工等整个生活史中发挥重要作用。
All mature protein generated from protease processing have important functions in the whole viral living cycle, including that polymerase, translation, and processing, etc.
结论应用半定量pcr方法可明显提高P CR -RFLP酶切法的精确性和可重复性。
Conclusion a higher level of consistency and repeatability was found from the method of semi-quantitative PCR-RFLP compared to PCR-RFLP.
锌指核酸酶被设计识别基因组特定DNA序列，之后对其进行酶切，进而删除或替换这段序列。
Zinc-finger nucleases are enzymes that can be designed to find specific DNA sequences in the genome and cut them out, deleting those sequences or swapping one gene for another.
结果构建的EBO G87和EBO WT重组载体经内切酶双酶切鉴定及核苷酸序列测定证实。
Results The constructed vectors of EBO-WT and EBO-G87 were identified by restriction enzyme digestion and nucleotide sequencing.
探讨和初步建立了利用双重pcr和双酶切技术同时检测esr、RYR1两个基因的变异的方法。
The duplex PCR and double digestion technique were established to detect polymorphisms of ESR and RYR1 simultaneously.
同时在连续传代40代后每隔5代提取重组病毒全基因组进行酶切鉴定，发现其酶切位点保持不变。
To evaluate its heredity stability, the recombinant virus genome was extracted and digested by Hindlll every 5 generations, and 40 generations later, its enzyme digestion sites almost keep stable.
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