Hrvatska znanstvena Sekcija img
3 gif
 O projektu
4 gif
Pregledavanje radova
Jednostavno pretraživanje
Napredno pretraživanje
Skupni podaci
Upis novih radova
Ispravci prijavljenih radova
Ostale bibliografije
Slični projekti
 Bibliografske baze podataka

Pregled bibliografske jedinice broj: 533186

Zbornik radova

Autori: Projić, Petar; Novokmet, Mislav; Lauc, Gordan; Škaro, Vedrana; Primorac, Dragan; Marjanović, Damir
Naslov: Population Studies at 11 Polymorphic STR Loci in a Bovine Sample from Northern Croatia
Izvornik: 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine: final program and abstractsZagreb : International Society for Applied Biological Sciences , 2011. 129-129.
Skup: 7th ISABS Conference in Forensic, Anthropologic and Medical Genetics
Mjesto i datum: Bol, Island of Brač, Croatia, 20-24. 06.2011.
Ključne riječi: bovine STR loci; Bos taurus; STR population studies; forensic DNA
Genotyping of polymorphic sites provides a unique DNA fingerprint. It is therefore possible to employ these methods to follow the meat samples along the retail chain, by generating a DNA profile that can be used to trace-back the identity of the individual animal from the carcasses or the meat cuts.DNA analysis from various type of samples originated from animal is still sort of challenge, especially when the meat cut or bone fragments are focal point of analysis. Applied Biosystems has developed STR kit that addresses the needs of the bovine DNA typing community and covers a common set of STR loci. Nevertheless, efficiency of existing commercial kit within Croatia still unknown and unexamined. Therefore we have performed Croatian cattle population study. Population studies included 111 randomly selected cattle (Bos taurus) from Northern Croatia. Genomic DNA was isolated from blood samples using BloodPrep™ Chemistry on the ABI PRISM6100 Nucleic Acid PrepStation™. Microsatellites were amplified using the StockMarks for Cattle® Bovine Genotyping Kit. The PCR amplification has been carried out in PE Gene Amp PCR System Thermal Cycler according to the manufacturer’s recommendations. The PCR products were submitted to fragments analysis by capillary electrophoresis, with an automated sequencer ABI PRISM 3130 genetic analyzer according to the manufacturer’s specifications. Results were read and interpreted using GeneMapper® ID Software v3.1., respectively. Microsatellite allelic frequency analysis was performed on these data using Cervus 3.0.3 The power of parental exclusion, expected and observed heterozygosity, probability of identity, and non-amplifying allele frequencies were calculated.
Vrsta sudjelovanja: Poster
Vrsta prezentacije u zborniku: Sažetak
Vrsta recenzije: Nema recenziju
Izvorni jezik: ENG
Kategorija: Znanstveni
Znanstvena područja:
Puni text rada: 533186.2011_7th_ISABS_Conference_page_129.pdf (tekst priložen 2. Stu. 2011. u 13:22 sati)
URL Internet adrese:
Upisao u CROSBI: (, 2. Stu. 2011. u 13:22 sati

Verzija za printanje   za tiskati