Evaluation of commercial forensic DNA extraction kits for decontamination and extraction of DNA from biological samples contaminated with radionuclides

2019 ◽  
Vol 302 ◽  
pp. 109867 ◽  
Author(s):  
Kaitlyn Toole ◽  
Paul Roffey ◽  
Emma Young ◽  
Kaymann Cho ◽  
Timothy Shaw ◽  
...  
2009 ◽  
Vol 54 (3) ◽  
pp. 599-607 ◽  
Author(s):  
Maxim G. Brevnov ◽  
Hemant S. Pawar ◽  
Janna Mundt ◽  
Lisa M. Calandro ◽  
Manohar R. Furtado ◽  
...  

2012 ◽  
Vol 57 (4) ◽  
pp. 1022-1030 ◽  
Author(s):  
Jason Y. Liu ◽  
Chang Zhong ◽  
Allison Holt ◽  
Robert Lagace ◽  
Michael Harrold ◽  
...  

Author(s):  
Agnieszka Parys-Proszek ◽  
Wojciech Branicki ◽  
Paulina Wolańska-Nowak ◽  
Tomasz Kupiec
Keyword(s):  

2020 ◽  
Author(s):  
Qi Wang ◽  
Xiaoxia Shen ◽  
Tian Qiu ◽  
Wei Wu ◽  
Zhian Wang ◽  
...  

Abstract Background CTAB has been considered as the standard protocol for DNA extraction. But the complex and time-consuming procedures can’t meet the needs of rapid molecular identification. The method of using cellulose filter paper strips to transfer the DNA in the plant tissue lysate to the nucleic acid amplification system shortening the DNA extraction time to 30 s. However, cellulose filter paper strips have some shortcomings that cannot be put into widespread use. And the data supporting the rapidly purification of DNA by cellulose filter paper is not sufficient.ResultsIn the study, the published filter paper strip was modified by sticking the filter paper on the PVC sheet. This modified method is named EZ-D, for easy DNA extraction. Compared with the original method, the DNA extracted by EZ-D is more efficient in PCR amplification. We also came up with a new DNA extraction buffer, which exhibited higher DNA extraction efficiency. When compared with classic CTAB, EZ-D also showed great advantages for higher efficiency, easier protocol and lower cost. PCR analyses showed that DNA extracted from several types of plants by EZ-D were appropriate for specific identification of biological samples. PCR using DNA extracted by EZ-D was sensitive enough to detect 0.1 ng/μL. Evaluation of the EZ-D showed that the DNA extracts can be successfully amplified by PCR reaction for the DNA fragments up to 3000 bp in length and up to 80% in GC content. EZ-D was successfully used for DNA extraction from a variety of plant species and plant tissues. Moreover, when EZ-D was combined with the loop-mediated isothermal amplification (LAMP) method, DNA identification of biological samples could be achieved in an equipment-free way. Conclusion Combined with DNA amplification technology, EZ-D protocol is a rapid, specific and sensitive method for molecular identification of plant samples. In addition, EZ-D method is the first application of cellulose filter paper in the identification of genetically modified crops and traditional Chinese medicine ultra-fine powder. In terms of practicability, EZ-D has realized the popularization of cellulose filter paper for rapid DNA purification in laboratories and markets.


2021 ◽  
Vol 32 (4) ◽  
Author(s):  
Jonathan Roth ◽  
Ilan Feine ◽  
Ortal Waiskopf ◽  
Ron Gafny ◽  
Merav Amiel

2006 ◽  
Vol 34 (2) ◽  
pp. 222-233 ◽  
Author(s):  
Frederick R. Bieber

Forensic data banks contain biological samples and DNA extracts as well as computerized databases of coded DNA profiles of convicted offenders, arrestees and crime scene samples. When used for investigative and law enforcement purposes, DNA data banks have been successful in providing key investigative leads in hundreds of criminal investigations. A number of these crimes would never have been resolved without use of such data banks. In addition, in some limited number of investigations, the exclusion of known suspects whose DNA profiles are known to be in an offender database can save valuable investigative time.Despite the above benefits, in hundreds of cases DNA samples are never collected and administrative and laboratory logjams delay prompt database searches. Furthermore, hundreds of DNA database matches (hits) languish, without any followup by law enforcement or prosecutors. These prevent or delay DNA matches and therefore can leave the public in grave risk of potential harm from recidivistic offenders who otherwise could have been apprehended and convicted if the process functioned more effectively.


2004 ◽  
Vol 141 (2-3) ◽  
pp. 149-151 ◽  
Author(s):  
I. Pfeiffer ◽  
I. Völkel ◽  
H. Täubert ◽  
B. Brenig

Author(s):  
V. Kallupurackal ◽  
T. Kausel ◽  
A. Sulzer ◽  
P. Voegeli ◽  
A. Kratzer
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document