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Gene disruption

HASHIGUCHI Kazunari kaz at kingyo.zool.kyoto-u.ac.jp
Fri Feb 2 06:06:56 EST 2001

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Dear all,

I am trying to preparate cerevisiae mutants, first time.  Use of
"Direct gene deletion by one-step PCR" method, I want to make
the linear DNA fragments, which is consists of (5' homologus
region - URA3 - 3' homologous region).  But I cannot design the
PCR primers.  Please tell me any attentions in this case.  I want
to use the template DNA, which is URA3 gene on YCp50, as a
making of cassette.



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