A simple method of DNA extraction from whole tissues and blood using glass powder for detection of transgenic animals by PCR

1995 ◽  
Vol 4 (2) ◽  
pp. 149-150 ◽  
Author(s):  
Joe Attal ◽  
Marco Cajero-Juarez ◽  
Louis-Marie Houdebine
2018 ◽  
Vol 1 (3) ◽  
pp. 27 ◽  
Author(s):  
Džiuginta Jakočiūnė ◽  
Arshnee Moodley

Bacteriophages (phages) are intensely investigated as non-antibiotic alternatives to circumvent antibiotic resistance development as well as last resort therapeutic options against antibiotic resistant bacteria. As part of gaining a better understanding of phages and to determine if phages harbor putative virulence factors, whole genome sequencing is used, for which good quality phage DNA is needed. Traditional phage DNA extraction methods are tedious and time consuming, requiring specialized equipment e.g., an ultra-centrifuge. Here, we describe a quick and simple method (under four hours) to extract DNA from double stranded DNA (dsDNA) phages at titers above 1.0 × 1010 plaque-forming units (PFU)/mL. This DNA was suitable for library preparation using the Nextera XT kit and sequencing on the Illumina MiSeq platform.


2006 ◽  
Vol 55 (9) ◽  
pp. 1187-1191 ◽  
Author(s):  
Lisa J. Griffiths ◽  
Martin Anyim ◽  
Sarah R. Doffman ◽  
Mark Wilks ◽  
Michael R. Millar ◽  
...  

Newer methods such as PCR are being investigated in order to improve the diagnosis of invasive aspergillosis. One of the major obstacles to using PCR to diagnose aspergillosis is a reliable, simple method for extraction of the fungal DNA. The presence of a complex, sturdy cell wall that is resistant to lysis impairs extraction of the DNA by conventional methods employed for bacteria. Numerous fungal DNA extraction protocols have been described in the literature. However, these methods are time-consuming, require a high level of skill and may not be suitable for use as a routine diagnostic technique. Here, a number of extraction methods were compared: a freeze–thaw method, a freeze–boil method, enzyme extraction and a bead-beating method using Mini-BeadBeater-8. The quality and quantity of the DNA extracted was compared using real-time PCR. It was found that the use of a bead-beating method followed by extraction with AL buffer (Qiagen) was the most successful extraction technique, giving the greatest yield of DNA, and was also the least time-consuming method assessed.


2010 ◽  
Vol 11 (9) ◽  
pp. 3149-3157 ◽  
Author(s):  
Ibrahim A. Arif ◽  
Mohammad A. Bakir ◽  
Haseeb A. Khan ◽  
Anis Ahamed ◽  
Ahmad H. Al Farhan ◽  
...  

2003 ◽  
Vol 48 (1) ◽  
pp. 2002184 ◽  
Author(s):  
Toshihiro Yasuda ◽  
Reiko Iida ◽  
Haruo Takeshita ◽  
Misuzu Ueki ◽  
Tamiko Nakajima ◽  
...  

2002 ◽  
Vol 20 (3) ◽  
pp. 299-299 ◽  
Author(s):  
Miguel Keb-Llanes ◽  
Gerardo González ◽  
Bartolomé Chi-Manzanero ◽  
Diógenes Infante

2005 ◽  
Vol 54 (1-6) ◽  
pp. 265-269 ◽  
Author(s):  
N. Colpaert ◽  
S. Cavers ◽  
E. Bandou ◽  
H. Caron ◽  
G. Gheysen ◽  
...  

Abstract The number of studies of tropical tree species that use molecular tools is increasing, most of which collect leaf tissue for genomic DNA extraction. In tropical trees the canopy is not only frequently inaccessible, but also, once reached, the leaf tissue is often heavily defended against herbivory by high concentrations of anti-predation compounds, which may inhibit downstream applications, particularly PCR. Cambium tissue, accessed directly from the tree trunk at ground level, offers a readily accessible resource that is less hampered by the presence of defensive chemicals than leaf tissue. Here we describe a simple method for obtaining tissue from the cambial zone for DNA extraction and test the applicability of the method in a range of tropical tree species. The method was used successfully to extract DNA from 11 species in nine families. A subset of the DNA extracts was tested in more detail and proved to be highly suitable for AFLP analysis.


1995 ◽  
Vol 76 (6) ◽  
pp. 578-581 ◽  
Author(s):  
M. Jaber ◽  
A. Rattan ◽  
A. Verma ◽  
J. Tyagi ◽  
R. Kumar

1991 ◽  
Vol 34 (1) ◽  
pp. 105-112 ◽  
Author(s):  
V.N. Loparev ◽  
M.A. Cartas ◽  
C.E. Monken ◽  
A. Velpandi ◽  
A. Srinivasan

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