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알파파 근류로부터 분리한 Poly ( A+ ) - mRNA 에 의하여 합성된 Leghemoglobin 유전자의 cDNA Cloning 에 관한연구
조무제,윤한대,최용락,최영주,이경상,Winstion J . Brill ( Moo Je Cho,Min Suk Yang,Han Dae Yun,Yong Lark Choi,Young Ju Choi,Kyung Sang Lee ) 생화학분자생물학회 1985 BMB Reports Vol.18 No.1
Complementary DNAs were synthesized by the leghemoglobin message rich 9S, 18S and 28S-mRNA fractions prepared from the poly(A)^+-mRNA of alfalfa root nodules. The synthetic Sal I linkered double stranded cDNA was inserted into the SalI site of the pBR322, and transformed in E. coli HB101. The leghemoglobin cDNA clones were screened by colony hybridization and Southern blot hybridization with the soybean leghemoglobin cDNA as a probe, and further screened by hybrid-released and hybridarrested translation. One alfalfa leghemoglobin cDNA clone was selected, and restriction map and fingerprints of the cDNA from the selected clone were analyzed.