Review



biorad dcode apparatus dgge  (Bio-Rad)


Bioz Verified Symbol Bio-Rad is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 96

    Structured Review

    Bio-Rad biorad dcode apparatus dgge
    Biorad Dcode Apparatus Dgge, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 3150 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/biorad dcode apparatus dgge/product/Bio-Rad
    Average 96 stars, based on 3150 article reviews
    biorad dcode apparatus dgge - by Bioz Stars, 2026-03
    96/100 stars

    Images



    Similar Products

    96
    Bio-Rad biorad dcode apparatus dgge
    Biorad Dcode Apparatus Dgge, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/biorad dcode apparatus dgge/product/Bio-Rad
    Average 96 stars, based on 1 article reviews
    biorad dcode apparatus dgge - by Bioz Stars, 2026-03
    96/100 stars
      Buy from Supplier

    96
    Bio-Rad biorad dcode dgge apparatus
    Fig. 2. <t>DGGE</t> gel of amplicons from PCR with isolated DNA and from filter PCR. The primers were GC358F and 907RM, which are specific for a portion of the 16S rRNA gene. The volume of the PCR reaction loaded in all sample lanes was the same. Arrow indicates a band found in the isolated DNA lane that is not obvious in the filter PCR lanes. Samples taken in November 1999
    Biorad Dcode Dgge Apparatus, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/biorad dcode dgge apparatus/product/Bio-Rad
    Average 96 stars, based on 1 article reviews
    biorad dcode dgge apparatus - by Bioz Stars, 2026-03
    96/100 stars
      Buy from Supplier

    Image Search Results


    Fig. 2. DGGE gel of amplicons from PCR with isolated DNA and from filter PCR. The primers were GC358F and 907RM, which are specific for a portion of the 16S rRNA gene. The volume of the PCR reaction loaded in all sample lanes was the same. Arrow indicates a band found in the isolated DNA lane that is not obvious in the filter PCR lanes. Samples taken in November 1999

    Journal: Aquatic Microbial Ecology

    Article Title: Structure of bacterial communities in aquatic systems as revealed by filter PCR

    doi: 10.3354/ame026013

    Figure Lengend Snippet: Fig. 2. DGGE gel of amplicons from PCR with isolated DNA and from filter PCR. The primers were GC358F and 907RM, which are specific for a portion of the 16S rRNA gene. The volume of the PCR reaction loaded in all sample lanes was the same. Arrow indicates a band found in the isolated DNA lane that is not obvious in the filter PCR lanes. Samples taken in November 1999

    Article Snippet: Electrophoresis was performed at 60°C for 20 h at 100 V using a BioRad Dcode DGGE apparatus.

    Techniques: Isolation

    Fig. 3. DGGE gel of amplicons from PCR with isolated DNA and from filter PCR. The primers were GC358F and 517R for a portion of the 16S rRNA gene. Standards (STD) were ampli- cons from 3 bacterial isolates. The volume of the PCR reaction loaded in all sample lanes was the same. Samples taken in May 2000

    Journal: Aquatic Microbial Ecology

    Article Title: Structure of bacterial communities in aquatic systems as revealed by filter PCR

    doi: 10.3354/ame026013

    Figure Lengend Snippet: Fig. 3. DGGE gel of amplicons from PCR with isolated DNA and from filter PCR. The primers were GC358F and 517R for a portion of the 16S rRNA gene. Standards (STD) were ampli- cons from 3 bacterial isolates. The volume of the PCR reaction loaded in all sample lanes was the same. Samples taken in May 2000

    Article Snippet: Electrophoresis was performed at 60°C for 20 h at 100 V using a BioRad Dcode DGGE apparatus.

    Techniques: Isolation

    Fig. 4. DGGE gel of 16S rRNA genes from pure bacterial isolates analyzed either separately or in mixtures. Isolates are given in Table 1. Mixtures consisted of: (1) the strains mixed together, fil- tered, and then subjected to filter PCR (F); (2) isolated DNA from each strain was mixed and then used a template in normal PCR (I); and (3) amplicons from the bacterial isolates were mixed after PCR in order to test the resolving power of the DGGE gel (C). Arrow indi- cates a band observed in the isolated DNA mixture that is not obvious in the mixed strain filter PCR lane

    Journal: Aquatic Microbial Ecology

    Article Title: Structure of bacterial communities in aquatic systems as revealed by filter PCR

    doi: 10.3354/ame026013

    Figure Lengend Snippet: Fig. 4. DGGE gel of 16S rRNA genes from pure bacterial isolates analyzed either separately or in mixtures. Isolates are given in Table 1. Mixtures consisted of: (1) the strains mixed together, fil- tered, and then subjected to filter PCR (F); (2) isolated DNA from each strain was mixed and then used a template in normal PCR (I); and (3) amplicons from the bacterial isolates were mixed after PCR in order to test the resolving power of the DGGE gel (C). Arrow indi- cates a band observed in the isolated DNA mixture that is not obvious in the mixed strain filter PCR lane

    Article Snippet: Electrophoresis was performed at 60°C for 20 h at 100 V using a BioRad Dcode DGGE apparatus.

    Techniques: Isolation