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K B Ignatov

Showing results (1-10 of 11) with videos related to

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Biochemistry. Biokhimiia|June 23, 2009
DNA ligases from thermophilic bacteria enhance PCR amplification of long DNA sequencesK B Ignatov, V M Kramarov
Bioorganicheskaia Khimiia|January 1, 1997
[Integration of IS186 element into the -10-region of the promoter of heat shock lon-gene in Escherichia coli]K B Ignatov, L G Chistiakova
FEBS Letters|April 29, 1998
Substitution of Asn for Ser543 in the large fragment of Taq DNA polymerase increases the efficiency of synthesis of long DNA moleculesK B Ignatov, A I Miroshnikov, V M Kramarov
Klinicheskaia Laboratornaia Diagnostika|February 1, 2019
[Comparative analysis of LAMP and Real Time PCR methods to detect pathogens of glanders and meliodosis.]I Yu Shchit, K B Ignatov, S F Biketov
Bioorganicheskaia Khimiia|September 2, 2003
[A new approach to enhance PCR specificity]K B Ignatov, A I Miroshnikov, V M Kramarov
FEBS Letters|April 27, 1999
Mutation S543N in the thumb subdomain of the Taq DNA polymerase large fragment suppresses pausing associated with the template structureK B Ignatov, A A Bashirova, A I Miroshnikov, et al.
Bioorganicheskaia Khimiia|March 7, 1998
[DNA polymerase mediated amplification of DNA fragments using primers with mismatches in the 3'-region]K B Ignatov, V M Kramarov, O L Uznadze, et al.
Bioorganicheskaia Khimiia|January 1, 1993
[Cloning the Staphylococcus aureus enterotoxin B gene, obtained by polymerase chain reaction, and its expression in Escherichia coli cells]K B Ignatov, L G Chistiakova, O B Shemchukova, et al.
Zhurnal Mikrobiologii, Epidemiologii I Immunobiologii|January 1, 1995
[The demonstration of the genes controlling enterotoxigenicity in Staphylococcus aureus strains by using the polymerase chain reaction]V V Grabovetskiĭ, K B Ignatov, L G Chistiakova, et al.
Biochemistry. Biokhimiia|July 26, 2005
Cloning and molecular modeling of duodenase with respect to evolution of substrate specificity within mammalian serine proteases that have lost a conserved active-site disulfide bondT S Zamolodchikova, E V Smirnova, A N Andrianov, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Biochemistry. Biokhimiia|June 23, 2009
DNA ligases from thermophilic bacteria enhance PCR amplification of long DNA sequencesK B Ignatov, V M Kramarov
Bioorganicheskaia Khimiia|January 1, 1997
[Integration of IS186 element into the -10-region of the promoter of heat shock lon-gene in Escherichia coli]K B Ignatov, L G Chistiakova
FEBS Letters|April 29, 1998
Substitution of Asn for Ser543 in the large fragment of Taq DNA polymerase increases the efficiency of synthesis of long DNA moleculesK B Ignatov, A I Miroshnikov, V M Kramarov
Klinicheskaia Laboratornaia Diagnostika|February 1, 2019
[Comparative analysis of LAMP and Real Time PCR methods to detect pathogens of glanders and meliodosis.]I Yu Shchit, K B Ignatov, S F Biketov
Bioorganicheskaia Khimiia|September 2, 2003
[A new approach to enhance PCR specificity]K B Ignatov, A I Miroshnikov, V M Kramarov
FEBS Letters|April 27, 1999
Mutation S543N in the thumb subdomain of the Taq DNA polymerase large fragment suppresses pausing associated with the template structureK B Ignatov, A A Bashirova, A I Miroshnikov, et al.
Bioorganicheskaia Khimiia|March 7, 1998
[DNA polymerase mediated amplification of DNA fragments using primers with mismatches in the 3'-region]K B Ignatov, V M Kramarov, O L Uznadze, et al.
Bioorganicheskaia Khimiia|January 1, 1993
[Cloning the Staphylococcus aureus enterotoxin B gene, obtained by polymerase chain reaction, and its expression in Escherichia coli cells]K B Ignatov, L G Chistiakova, O B Shemchukova, et al.
Zhurnal Mikrobiologii, Epidemiologii I Immunobiologii|January 1, 1995
[The demonstration of the genes controlling enterotoxigenicity in Staphylococcus aureus strains by using the polymerase chain reaction]V V Grabovetskiĭ, K B Ignatov, L G Chistiakova, et al.
Biochemistry. Biokhimiia|July 26, 2005
Cloning and molecular modeling of duodenase with respect to evolution of substrate specificity within mammalian serine proteases that have lost a conserved active-site disulfide bondT S Zamolodchikova, E V Smirnova, A N Andrianov, et al.
Pageof 2