skip navigation

CrimeSolutions.gov

Add your conference to our Justice Events calendar

PUBLICATIONS

NCJRS Abstract

The document referenced below is part of the NCJRS Library collection.
To conduct further searches of the collection, visit the NCJRS Abstracts Database.

How to Obtain Documents
 
NCJ Number: NCJ 236537   Add to Shopping cart   Find in a Library
Title: Forensic Stain Identification By RT-PCR Analysis (Updated)
Author(s): Trisha Conti, Ph.D. ; Eric Buel, Ph.D.
Date Published: 2011
Page Count: 88
Sponsoring Agency: National Institute of Justice
US Department of Justice
Office of Justice Programs
United States of America
Grant Number: 2007-DN-BX-K149
Sale Source: National Institute of Justice/NCJRS
Box 6000
Rockville, MD 20849
United States of America

NCJRS Photocopy Services
Box 6000
Rockville, MD 20849-6000
United States of America
Document: PDF 
Type: Report (Study/Research)
Language: English
Country: United States of America
Annotation: This report describes the methodology and findings of a project that developed a RNA/DNA co-isolation technique that extracts both nucleic acids of sufficient quality and quantity for downstream real-time PCR and STR analyses.
Abstract: The project’s first goal was to identify the best method to co-extract DNA and RNA from a variety of stain types. By using one extraction step, a DNA sample would be ready and waiting for STR profiling if the RNA screening assay deemed it worthy of such analysis. In addition, obtaining RNA and DNA from a single stain would present the possibility of conclusions being drawn regarding the identity of one stain that may hot hold true for a nearby stain. Based on preliminary experiments, the TRIzol method was identified as an efficient and straight-forward procedure for the isolation of DNA and RNA. Still, there are several disadvantages which caused researchers to seek an alternative isolation procedure. A homebrew extraction method was developed that worked for RNA and DNA. It is faster than the TRIzol method and produces significantly better DNA yields. The project then identified gene candidates that were specific for each tissue of interest. The candidates used throughout the project were identified through literature review, Gene, and other databases. Researchers tested the specificity and sensitivity of each assay by analysis of mRNA isolated from the body fluid of interest (seminal fluid) or control RNA (brain). The diverse sample bank was used to assess the specificity of the candidate tissue-specific genes. These samples included blood, semen, saliva, menstrual blood vaginal secretions, kidney, colon, adipose, skin and control human RNAs (brain, heart, liver, kidney, and intestine). The completion of project components produced the conclusion that DNA and RNA can be co-extracted and the RNA fraction used in multiplexed real-time PCR assays. 3 figures and 39 references
Main Term(s): Police policies and procedures
Index Term(s): Victim identification ; Suspect identification ; Blood/body fluid analysis ; Blood stains ; DNA fingerprinting ; NIJ final report
   
  To cite this abstract, use the following link:
https://www.ncjrs.gov/App/Publications/abstract.aspx?ID=258544

* A link to the full-text document is provided whenever possible. For documents not available online, a link to the publisher's web site is provided.