Results 181 to 190 of about 655,509 (235)
An application of PCR-RFLP species identification assay for environmental DNA detection. [PDF]
PeerJ, 2019 Igawa T, Takahara T, Lau Q, Komaki S.
europepmc +1 more source
Molecular identification of biwa trout (Oncorhynchus masou rhodurus) using PCR-RFLP method. [PDF]
J Food Sci Technol, 2019 Matsumoto C +6 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Differentiation of sturgeon species by PCR-RFLP
Food Research International, 1999Abstract A method for identification of sturgeon species in caviar has been developed based on the amplification of a region of the mitochondrial genome (tRNAGlu/cytochrome b) using the polymerase chain reaction (PCR). To distinguish between several types of sturgeon caviar the obtained 462bp long PCR-products were cut with different restriction ...
P Hübner, Jürg Luthy
exaly +2 more sources
PCR-RFLP for Aspergillus Species
2016Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) is the most simple method for single-nucleotide change detection. It is widely used in the detection and differentiation between mycotoxigenic species. It is based on PCR amplification of a target region containing the variant site of the studied species followed by ...
Ali, Atoui, André, El Khoury
openaire +2 more sources
Automated, PCR-RFLP Genotyping of the Urokinase Gene
Genetic Testing, 2000The urokinase-type plasminogen activator (u-PA) has been suggested to play a role in the early initiation and progression of atherosclerosis and coronary artery disease (CAD) (Grenett et aL, 1998). Recently, a common genetic polymorphism in the untranslated region of the u-PA gene was shown to be associated with syptomatic CAD.
S M, Sell, F, Blasi, F, Booyse
openaire +2 more sources
Comprehensive typing of DQB1 alleles by PCR‐RFLP
Tissue Antigens, 1994Abstract: The protocols represented in this report can resolve all 22 DQB1 alleles. The second exon of DQB1 was subjected to PCR using two group‐specific primers to obtain DQB1 group 1 (DQ5 and DQ6) and group 2 (DQ2, DQ3, DQ4) specific amplified products, respectively.
D P, Sengar, R, Goldstein
openaire +2 more sources
Identification of clinically relevant yeasts by PCR/RFLP
Journal of Microbiological Methods, 2004For molecular diagnosis of fungal disease using DNA amplification procedures in the routine laboratory, choice of appropriate target structures and rapid and inexpensive identification of amplification products are important prerequisites. Most diagnostic procedures described thus far are characterized by limited applicability, considerable cost for ...
Anja, Trost +6 more
openaire +2 more sources
Discrimination of Penaeid Shrimps with PCR-RFLP Analysis
Journal of Shellfish Research, 2008Abstract A rapid polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analysis was designed to examine genetic differentiation of some penaeid shrimps. Three hundred and fifty-six bp of cytochrome-b gene, a specific part of mitochondrial genome, was amplified with PCR to figure out differences between shrimp species Penaeus ...
HİSAR, OLCAY +4 more
openaire +3 more sources
Identification of common species of dermatophytes by PCR-RFLP
Journal of Huazhong University of Science and Technology [Medical Sciences], 2005To establish a simple, sensitive and effective technique for the identification of six common dermatophytes, polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (RFLP) targeting Topoisomerase II gene were used. The DNA of 6 common dermatophytes was amplified by primer dPsD1 and then primers dPsD2.
Ganlin, He +3 more
openaire +2 more sources