Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Attenuation of PCR inhibition in the presence of plant compounds by addition of BLOTTO.

Literature DB >> 7630739

Attenuation of PCR inhibition in the presence of plant compounds by addition of BLOTTO.

S H De Boer¹, L J Ward, X Li, S Chittaranjan.

Abstract

Mesh：

Substances：

Year: 1995 PMID： 7630739 PMCID： PMC307069 DOI： 10.1093/nar/23.13.2567

Source DB: PubMed Journal: Nucleic Acids Res ISSN： 0305-1048 Impact factor: 16.971

× No keyword cloud information.

3 in total

1. Detection of low numbers of bacterial cells in soils and sediments by polymerase chain reaction.

Authors: Y L Tsai; B H Olson
Journal: Appl Environ Microbiol Date: 1992-02 Impact factor: 4.792

2. Detection of enteroviruses in groundwater with the polymerase chain reaction.

Authors: M Abbaszadegan; M S Huber; C P Gerba; I L Pepper
Journal: Appl Environ Microbiol Date: 1993-05 Impact factor: 4.792

3. Quantitative cell lysis of indigenous microorganisms and rapid extraction of microbial DNA from sediment.

Authors: M I Moré; J B Herrick; M C Silva; W C Ghiorse; E L Madsen
Journal: Appl Environ Microbiol Date: 1994-05 Impact factor: 4.792

3 in total

9 in total

1. Extraction-free, filter-based template preparation for rapid and sensitive PCR detection of pathogenic parasitic protozoa.

Authors: P A Orlandi; K A Lampel
Journal: J Clin Microbiol Date: 2000-06 Impact factor: 5.948

2. Methodological Guidelines for Accurate Detection of Viruses in Wild Plant Species.

Authors: Christelle Lacroix; Kurra Renner; Ellen Cole; Eric W Seabloom; Elizabeth T Borer; Carolyn M Malmstrom
Journal: Appl Environ Microbiol Date: 2016-01-15 Impact factor: 4.792

3. Development of an efficient real-time quantitative PCR protocol for detection of Xanthomonas arboricola pv. pruni in Prunus species.

Authors: Ana Palacio-Bielsa; Jaime Cubero; Miguel A Cambra; Raquel Collados; Isabel M Berruete; María M López
Journal: Appl Environ Microbiol Date: 2010-10-29 Impact factor: 4.792

4. Comparison of rapid quantitative PCR-based and conventional culture-based methods for enumeration of Enterococcus spp. and Escherichia coli in recreational waters.

Authors: Rachel T Noble; A Denene Blackwood; John F Griffith; Charles D McGee; Stephen B Weisberg
Journal: Appl Environ Microbiol Date: 2010-09-24 Impact factor: 4.792

5. Divergent arbuscular mycorrhizal fungal communities colonize roots of Pulsatilla spp. in boreal Scots pine forest and grassland soils.

Authors: Maarja Öpik; Mari Moora; Jaan Liira; Urmas Kõljalg; Martin Zobel; Robin Sen
Journal: New Phytol Date: 2003-12 Impact factor: 10.151

Attenuation of PCR inhibition in the presence of plant compounds by addition of BLOTTO.

1. Detection of low numbers of bacterial cells in soils and sediments by polymerase chain reaction.

2. Detection of enteroviruses in groundwater with the polymerase chain reaction.

3. Quantitative cell lysis of indigenous microorganisms and rapid extraction of microbial DNA from sediment.

1. Extraction-free, filter-based template preparation for rapid and sensitive PCR detection of pathogenic parasitic protozoa.

2. Methodological Guidelines for Accurate Detection of Viruses in Wild Plant Species.

3. Development of an efficient real-time quantitative PCR protocol for detection of Xanthomonas arboricola pv. pruni in Prunus species.

4. Comparison of rapid quantitative PCR-based and conventional culture-based methods for enumeration of Enterococcus spp. and Escherichia coli in recreational waters.

5. Divergent arbuscular mycorrhizal fungal communities colonize roots of Pulsatilla spp. in boreal Scots pine forest and grassland soils.

6. Inactivation of Cryptosporidium parvum oocysts in fresh apple cider by UV irradiation.

7. Use of lambda phage DNA as a hybrid internal control in a PCR-enzyme immunoassay to detect Chlamydia pneumoniae.

8. Engineered DNA polymerase improves PCR results for plastid DNA.

9. qPCR, dPCR, NGS - A journey.