用本法检测参考虫株出现的带型和长度与设计的靶序列完全吻合。
The sizes and patterns of the bands produced by the reference strains were consistent with those of designed target sequences.
在锤头型核酶下游增加一段核酶作用的靶序列，使之成为自切割的核酶。
A self cleaving ribozyme was comprised of a hammerhead ribozyme and its target sequence located the downstream of the hammerhead ribozyme.
利用PCR 方法标记待检测的靶序列，与玻片表面的探针进行固相杂交。
Target sequences labeled by PCR were hybridized with probes on glass slide.
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