Study on optimization of SRAP-PCR reaction system for Pinellia ternata in Suzhou / 中国中药杂志
Zhongguo Zhong Yao Za Zhi
; (24): 3815-3818, 2012.
Article
ي Zh
| WPRIM
| ID: wpr-346831
المكتبة المسؤولة:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the optimization system of SRAP-PCR molecular marker technology in the analysis on Pinellia ternata.</p><p><b>METHOD</b>SRAP-PCR reaction system for P. ternata was optimized by L16 (5(4)) orthogonal design with five elements (dNTPs, Mg2+, the template DNA, primers, Taq enzyme) and four standards.</p><p><b>RESULT</b>The most suitable forward primer for SRAP for Pinellia ternata was 5'-TGAGTCCAAACCGGAAG-3', while the reverse primer was 5'-GACTGCGTACGAATTACG-3'. The optimized reaction system contained 70 ng DNA template, 0.9 micromol x L(-1) primer, 0.20 mmol x L(-1) dNTP s, 1.5 - 2.0 mmol x L(-1) Mg2+, and 2 U Taq enzyme.</p><p><b>CONCLUSION</b>SRAP-PCR system for P. ternata is established to lay a foundation for future construction of SRAP genetic map of P. ternata.</p>
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Templates, Genetic
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China
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Polymerase Chain Reaction
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Reproducibility of Results
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DNA Primers
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DNA, Plant
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Taq Polymerase
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Nucleic Acid Amplification Techniques
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Pinellia
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Electrophoresis
البلد/الأقليم حسب الموضوع:
Asia
اللغة:
Zh
مجلة:
Zhongguo Zhong Yao Za Zhi
السنة:
2012
نوع:
Article