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1·Differential DNA dot hybridization of subtractive cDNA clones.

差减阳性克隆的斑点杂交。

2·Aim: Cloning and sequencing of hOP-1 cDNA encoding mature protein.

目的：克隆成骨蛋白-1（OP-1）成熟蛋白编码区基因。

3·Aim: To clone MAR-binding protein cDNA fragment from Dunaliella salina.

目的：克隆杜氏盐藻核基质附着区(MAR)结合蛋白片段。

4·The lengths of the double stranded cDNA fragments were about 500 base pairs.

其双链链长，经凝胶电泳分析，约为500碱基对。

5·AIM: To clone and analyze the cDNA encoding immunodiagnostic antigen of cysticercosis.

目的：克隆与分析囊虫病诊断用抗原及其编码基因。

6·Conclusion a eukaryotic system that expressing mutant CD59 cDNA was successfully set up.

结论建立了两个高效表达突变CD 59的真核表达系统，获得阳性克隆细胞株。

7·Conclusion: cDNA microarray found the tumor specific gene expression spectrum in gliomas.

结论：基因芯片发现了胶质瘤的异常基因表达谱。

8·Based on sequence homology, it was suggested that the obtained cDNA was a SAM gene in tea plant.

证实所获得的基因序列为茶树SAM合成酶基因。

9·Objective To clone the cDNA of the preprotein cDNA of human bone morphogenetic protein 12 (hBMP12).

目的克隆人骨形态发生蛋白12前体蛋白的基因。

10·Conclusion: The cloned sequence is probably MAR binding protein cDNA fragment from Dunaliella salina.

结论：所克隆的序列可能为杜氏盐藻MAR结合蛋白片段。