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Mirck, M. H., Von Bannisseht-Wijsmuller, T. H., Timmermans-Besselink, W. J. H., Van Luijk, J. H. L., Buntjer, J. B. and Lenstra, J. A. (1995): Optimization of the PCR test for the mutation causing bovine leukocyte adhesion deficiency. Cell. Mol. Biol
deoxyribonucleic acid (DNA) from bloodstains, a major inhibitor of polymerase chain reaction (PCR) amplification . J. Forensic Sci. 39 , 362 – 372 . Ayling , R. , Regalla , J. , Spencer , Y
phenotypic methods such as Carbapenem Inactivation Method, Modified Hodge Test, inhibitor-based methods, biochemical methods and genotypic methods such as PCR, cloning and sequencing should be performed [ 9 , 10 ]. Methods Enterobacterales species isolated
investigation of carbapenemases gene detection. PCR amplification was carried out for the detection of carbapenemases genes ( bla KPC , bla NDM, bla BIC, bla IMP, bla VIM , bla SPM, bla AIM, bla DIM, bla GIM, bla SIM, and bla OXA-48 ) with an
application of an accurate and reliable diagnostic technique like polymerase chain reaction (PCR) is necessary [ 1 , 3 , 11 , 18 , 19 ]. Hence, in this study the authors tried to detect and identify the distribution of four important virulence
dogs that had died as a result of CDV infection. We used molecular virological and immunohistochemical methods to update the information about CDV infection and the circulating strains in our country based on partial sequences, obtained by PCR from the
A SARS-CoV-2-járvány kihívásai és tapasztalatai a molekuláris diagnosztikában
Challenges and experiences of the SARS-CoV-2 pandemic in molecular diagnostics
References 1 Tresó B. Real-time PCR. In: Takács M. (ed.) Clinical and epidemiological virology. [Real-time PCR. In: Takács M. (szerk.) Klinikai és
, 679 – 693 . Drén , Cs. N. , Koch , G. , Kant , A. , Verschueren , C. A. J. , van der Eb , A. J. and Noteborn , M. H. M. ( 1994 ): A hot start PCR for the laboratory
applicable for diagnosing microfilaraemia without definitive distinction of D. immitis and D. repens ( Magnis et al., 2013 ). The polymerase chain reaction (PCR) technique as a molecular biological method can be considered the most sensitive
1787 1792 Costa, L. M., Pautas, C., Ernault, P. és mtsai: Real-time PCR for diagnosis and follow-up of Toxoplasma reactivation after allogeneic stem cell
