The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接序,确认基因型果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要仪器就是核酸扩增热循环仪（PCR仪，实时荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环仪都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

果表明,建立多重PCR方法能够准确同时检出豆粕中基因和转基因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接序,确认基因型定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要仪核酸扩增热循环仪（PCR仪，实荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环仪都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立多重PCR方法能够准确同出豆粕中内源基因和转基因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合终止法进行PCR产物直接测,型测定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要仪器就是核酸扩增热循环仪（PCR仪，实时荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环仪都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立多重PCR方法能够准同时检测出豆粕中内源和转分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检测假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要器就是核酸扩增热循环（PCR，荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立PCR方法能够准确同检测出豆粕中内源基因和转基因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检测假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物序,确认基因型定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要仪器就是核酸扩增热循环仪（PCR仪，实时荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环仪都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立多重PCR方法能够准确同时检出豆粕中内源基因和转基因成。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要器就是核酸扩增热循环（PCR，荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立PCR方法能够准确同检测出豆粕中内源基因和转基因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检测假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要仪器就是酸扩增热循环仪（PCR仪，实时荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环仪都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立多重PCR方法能够准确同时检测出豆粕中内源基因和转基因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬酸样品制备效率低难题,有效地避免了PCR检测假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要器就是核酸扩增热循环（PCR，实时荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立多重PCR方法能够准确同时检测出豆粕中内源基因和转基因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检测假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接序,确认因型结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要仪器就是核酸扩增热循环仪（PCR仪，实时荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合能快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf热循环仪都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立多重PCR方法能够准确同时检出豆粕中因和转因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检假阴性反应。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基因型测定结果。

The main equipment here is a thermal cycler system for nucleic acid amplification (PCR, quantitative fluorescence detection or common).

主要仪器就是核酸扩环仪（PCR仪，实时荧光或普通）。

Furthermore, sugarcane ratoon stunning disease pathogen can be rapidly detected by means of television phase contrast microscope and PCR.

利用电视相差显微镜和PCR技术结合快速诊断甘蔗宿根矮化病。

The Eppendorf Thermal Cycler is an Authorized Thermal Cycler and may be used with PCR licenses available from Applied Biosystems.

Eppendorf环仪都具有美国应用生物系统公司颁发PCR试验专利授权。

The results showed that the high efficiency PCR system can differentially,conveniently,effectively and coinstantaneously examine the endogenous gene Lectin and the transgenic components.

结果表明,建立多重PCR方法确同时检测出豆粕中内源基因和转基因成分。

This method resolved the problem of poor yield of DNA from smut teliospore thick wall, and efficiently avoided the false negative result of PCR.

此法解决了腥黑穗菌厚壁冬孢子核酸样品制备效率低难题,有效地避免了PCR检测假阴性反应。