Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems

ISSN:
0006-291X
Source:
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
Topics:
Biology
Chemistry and Pharmacology
Physics
Type of Medium:
Electronic Resource
URL:
_version_ 1798292235894128642
autor Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
autorsonst Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
book_url http://dx.doi.org/10.1016/0006-291X(90)92136-N
datenlieferant nat_lic_papers
fussnote Our purpose was to identify individuals from blood stains in two murder cases. We used primers flanking the hypervariable region of the apoB gene to amplify DNA extracted from blood stains and blood samples from suspected persons. The sensitivity and specificity of the procedure was improved by carrying out two consecutive PCR amplifications with a nested set of primers in the second amplification. The size of the generated fragments was determined by polyacrylamide gel electrophoresis followed by staining with ethidium bromide. By comparing the fragments produced from the stains with those from the blood samples we were able to identify the origin of the blood stains in both cases.
hauptsatz hsatz_simple
identnr NLZ184082021
issn 0006-291X
journal_name Biochemical and Biophysical Research Communications
materialart 1
package_name Elsevier
publikationsort Amsterdam
publisher Elsevier
reference 170 (1990), S. 616-620
search_space articles
shingle_author_1 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
shingle_author_2 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
shingle_author_3 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
shingle_author_4 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
shingle_catch_all_1 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
0006-291X
0006291X
Elsevier
shingle_catch_all_2 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
0006-291X
0006291X
Elsevier
shingle_catch_all_3 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
0006-291X
0006291X
Elsevier
shingle_catch_all_4 Vuorio, A.F.
Sajantila, A.
Hamalainen, T.
Syvanen, A.-C.
Ehnholm, C.
Peltonen, L.
Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
0006-291X
0006291X
Elsevier
shingle_title_1 Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
shingle_title_2 Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
shingle_title_3 Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
shingle_title_4 Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
sigel_instance_filter dkfz
geomar
wilbert
ipn
albert
fhp
source_archive Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
timestamp 2024-05-06T08:45:18.526Z
titel Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
titel_suche Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems
Our purpose was to identify individuals from blood stains in two murder cases. We used primers flanking the hypervariable region of the apoB gene to amplify DNA extracted from blood stains and blood samples from suspected persons. The sensitivity and specificity of the procedure was improved by carrying out two consecutive PCR amplifications with a nested set of primers in the second amplification. The size of the generated fragments was determined by polyacrylamide gel electrophoresis followed by staining with ethidium bromide. By comparing the fragments produced from the stains with those from the blood samples we were able to identify the origin of the blood stains in both cases.
topic W
V
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uid nat_lic_papers_NLZ184082021