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Yvaine830

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Why not using the CTAB Method?

3% CTAB DNA extraction protocol http://www.zoology.ubc.ca/~riese ... n-protocol-v1.2.pdf
2Â¥2016-01-07 12:01:55
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Yvaine830

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ÒýÓûØÌû:
2Â¥: Originally posted by ·´Ó¦Á´ at 2016-01-07 12:01:55
Why not using the CTAB Method?

3% CTAB DNA extraction protocol http://www.zoology.ubc.ca/~rieseberg/RiesebergResources/wp-content/uploads/2013/03/Sunflower-CTAB-DNA-extraction-protocol-v1.2.pdf...

ÀÏʦҪÇóÎÒÃÇÓÃÕâÖÖ·½·¨ ÎÒ¾ÍÏëÎÊÎÊΪʲô»áÕâÑù ¸Ð¾õÊÇÌá³ödnaÁË ÒòΪ°ÑÄǸöÓÍ×´Îï¼Óµ½ÇíÖ¬ÌÇÀïËü»áÁÁ ¾ÍÊDz»ÈÜÓÚȾÁÏ Ò²²»ÍùÏÂÅÜ

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3Â¥2016-01-08 14:00:48
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ÒýÓûØÌû:
3Â¥: Originally posted by Yvaine830 at 2016-01-08 14:00:48
ÀÏʦҪÇóÎÒÃÇÓÃÕâÖÖ·½·¨ ÎÒ¾ÍÏëÎÊÎÊΪʲô»áÕâÑù ¸Ð¾õÊÇÌá³ödnaÁË ÒòΪ°ÑÄǸöÓÍ×´Îï¼Óµ½ÇíÖ¬ÌÇÀïËü»áÁÁ ¾ÍÊDz»ÈÜÓÚȾÁÏ Ò²²»ÍùÏÂÅÜ
...

Your DNA samples are rich in sticky compounds. You should wash the homogenate with CTAB-free buffer for three or four times, until the supernatant is not viscous.

Please refer to this article "Zeng J, Zou Y P, Bai J Y, et al. Preparation of total DNA from ¡®recalcitrant plant taxa¡¯[J]. Acta Botanica Sinica, 2002, 44(6): 694-697."

"The DNA is in a tight tangle with polysaccharides. This tangle of DNA and polysaccharides is very difficult to separte, which has make them too sticking to be dissolved in water or TE, and it is not even possible to load such DNA samples into the electrophoresis well. "

Therefore, your protocol is not suitable for the plant total DNA extraction. Give you a advise, use the 3% CTAB DNA extraction protocol instead.
4Â¥2016-01-08 15:14:02
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