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In this study, we used a two-step PCR protocol as previously described (19). With this approach, tags and adapters were added in a second round of PCR amplification. This method facilitates DNA amplification from complex biological samples (20), increases reproducibility, and recovers higher genetic diversity, avoiding the amplification bias that is introduced by using long fusion primers in one-step PCR amplification¡£ ÎÒÊÇС°×Ò»¸ö£¬ÕâÀïÃæµÄtag ºÍadapter·Ö±ðÊÇʲôÒâ˼°¡£¿»¹ÓУ¬×îÖ÷ÒªµÄ:Õâ¸ötwo-step PCR ÊÇÒ»¸öʲô·½·¨£¬Äܲ»Äܾ;ßÌ彲һϣ¬ÒòΪҪÏòÀÏʦ»ã±¨ÕâÆªÎÄÕ£¬µ«ÊǶÔÕâ¸öÍêÈ«²»Á˽Ⱑ£¬È¥ÄÄÀïÕÒÕÒÕâ·½ÃæµÄ×ÊÁÏ£¿ |
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- Ìû×Ó: 2059
- ÔÚÏß: 511.5Сʱ
- ³æºÅ: 3326118
- ×¢²á: 2014-07-16
- ÐÔ±ð: GG
- רҵ: »·¾³ÎÛȾ»¯Ñ§
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¶î¶î£¬²»ºÃÒâ˼£¬The first PCR amplification was performed using the modified primers 341F (CCTAYGGGRBGCASCAG) and 806R (GGACTACNNGGGTATCTAAT) (20) to amplify a 466-bp fragment of the 16S rRNA gene flanking the V3 and V4 regions. The PCR mix (40 l) contained 1Phusion HF buffer containing 2.5 mM MgCl2 (Finnzymes, Vantaa, Finland),0.2mMdeoxynucleoside triphosphate (dNTP) mixture, 0.8UPhusion hot start DNA polymerase, 2 M each primer, 25 g bovine serum albumin (BSA; molecular grade, 10 mg ml1 stock), and 1 l template.ÏÈÊÇÀ©ÔöµÄ16S rRNA£¬È»ºóÓÃÕâ¸öDNA½øÐеĵڶþÂÖÀ©Ôö£¬Ó¦¸Ã¾ÍÊÇRT-PCRÁ˰ɡ£¡£¡£ |
14Â¥2014-12-18 21:56:12
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- ×¢²á: 2014-08-14
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Kobe¾ýÁÙÌìÏÂ: ½ð±Ò+2, ¡ïÓаïÖú 2014-12-18 14:24:41
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Kobe¾ýÁÙÌìÏÂ: ½ð±Ò+2, ¡ïÓаïÖú 2014-12-18 14:24:41
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2Â¥2014-12-18 11:50:39
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- Ó¦Öú: 70 (³õÖÐÉú)
- ½ð±Ò: 1818.6
- ºì»¨: 11
- Ìû×Ó: 267
- ÔÚÏß: 127.3Сʱ
- ³æºÅ: 3365870
- ×¢²á: 2014-08-14
- רҵ: ÉúÎï´ó·Ö×ӽṹÓ빦ÄÜ
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Kobe¾ýÁÙÌìÏÂ: ½ð±Ò+2, ¡ïÓаïÖú 2014-12-18 14:26:14
Kobe¾ýÁÙÌìÏÂ: ½ð±Ò+2, ¡ïÓаïÖú 2014-12-18 14:26:14
3Â¥2014-12-18 11:54:01
Kobe¾ýÁÙÌìÏÂ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 10 (Ó×¶ùÔ°)
- ½ð±Ò: 7145.4
- É¢½ð: 422
- ºì»¨: 12
- Ìû×Ó: 2059
- ÔÚÏß: 511.5Сʱ
- ³æºÅ: 3326118
- ×¢²á: 2014-07-16
- ÐÔ±ð: GG
- רҵ: »·¾³ÎÛȾ»¯Ñ§
4Â¥2014-12-18 14:26:02














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