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1.
Sci Justice ; 59(4): 411-417, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-31256812

RESUMO

The RapidHIT™ 200 device from IntegenX® provides a sample-to-profile platform that is capable of processing a variety of sample types. In this study we review the sensitivity of the 'Run Other' protocol for processing crime stain type samples containing various input quantities of DNA using the AmpFℓSTR® NGMSElect™ Express PCR Amplification Kit cartridges available from IntegenX®. The range of DNA inputs which achieved useable results were not as desired and therefore various enhancements to the instruments extraction processes were investigated. These studies showed an improvement in the range of DNA input templates that could by processed on the RapidHIT™ 200 by using the enhanced methods and resulted in three new run protocols.


Assuntos
Impressões Digitais de DNA/instrumentação , Impressões Digitais de DNA/métodos , Moldes Genéticos , Alelos , Manchas de Sangue , Linhagem Celular , Humanos , Masculino , Reação em Cadeia da Polimerase em Tempo Real
2.
Forensic Sci Int ; 289: 244-252, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-29908518

RESUMO

The RapidHIT™ 200 System is a fully automated sample-to-DNA profile system designed to produce high quality DNA profiles within 2h. The use of RapidHIT™ 200 System within the United Kingdom Criminal Justice System (UKCJS) has required extensive development and validation of methods with a focus on AmpFℓSTR® NGMSElect™ Express PCR kit to comply with specific regulations for loading to the UK National DNA Database (NDNAD). These studies have been carried out using single source reference samples to simulate live reference samples taken from arrestees and victims for elimination. The studies have shown that the system is capable of generating high quality profile and has achieved the accreditations necessary to load to the NDNAD; a first for the UK.


Assuntos
Impressões Digitais de DNA , DNA/isolamento & purificação , Genética Forense/instrumentação , Mucosa Bucal/química , Bases de Dados de Ácidos Nucleicos , Humanos , Reação em Cadeia da Polimerase , Reprodutibilidade dos Testes , Manejo de Espécimes , Reino Unido
3.
Forensic Sci Int Genet ; 13: 195-205, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25178681

RESUMO

The PowerPlex(®) ESI 16 Fast, ESI 17 Fast, ESX 16 Fast, and ESX 17 Fast Systems represent faster cycling versions (50min or less) of the PowerPlex(®) ESI and ESX Systems released by Promega in 2009 to accommodate the ENFSI and EDNAP groups' call for new STR multiplexes for Europe. In addition to amplification of purified DNA samples, these new faster cycling systems allow for direct amplification from single-source blood and buccal samples deposited on FTA(®) and nonFTA paper as well as from SwabSolution™ extracts of buccal swabs without the need for purification and quantitation. There are no changes to the autosomal primer pair sequences in the PowerPlex(®) ESI Fast and ESX Fast Systems compared to the original multiplexes, and full concordance at all autosomal loci and amelogenin was observed with data generated previously with the original PowerPlex(®) ESI and ESX Systems. This paper describes the developmental validation study performed on these new fast systems following guidelines issued by the Scientific Working Group on DNA Analysis Methods (SWGDAM) and those of the DNA Advisory Board (DAB). Validation data demonstrate that these systems are sensitive for detecting low levels of DNA while also being capable of generating robust profiles from the high amount of input DNA present in direct-amplification samples. These systems are also tolerant to both high concentrations of PCR inhibitors as well as to slight variations in the final concentration of master mix and primer pair present in the amplification reaction that might be encountered due to pipetting error. The results of this validation study demonstrate that these systems may be used on multiple thermal cyclers and capillary electrophoresis platforms.


Assuntos
Impressões Digitais de DNA , Repetições de Microssatélites , Reação em Cadeia da Polimerase Multiplex/instrumentação , Animais , Degradação Necrótica do DNA , Eletroforese Capilar , Humanos , Masculino , Reprodutibilidade dos Testes , Especificidade da Espécie , Manejo de Espécimes/métodos
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