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Dna Rna

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Dna Rna Hay 31638 productos

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  • DNA Marker Low is useful for determination of DNA fragments 50 bp to 1,000 bp in size. The DNA size marker consists of 10 double-stranded, blunt-end DNA fragments. The DNA bands close to each other, 550 bp and 500 bp, 120 bp and 100 bp, are for reference indicators. These DNA fragments were fixed amount in solution of DNA Marker Low, which makes it...

  • DNA Marker High is useful for determination of DNA fragments 300 bp to 10,000 bp in size. The DNA size marker consists of 13 double-stranded, blunt-end DNA fragments. The DNA bands close to each other, 525 bp and 500 bp, are for reference indicators. These DNA fragments were fixed amount in solution of DNA Marker High, which makes it possible to estimate...

  • DNA Marker Middle is useful for determination of DNA fragments cloned in a plasmid DNA. The DNA size marker consists of 14 double-stranded, blunt-end DNA fragments. The size of 2, 686 bp fragment is the same size of pUC18/19. The DNA bands close to each other, 2, 686 and 3,000 bp, 550 bp and 500 bp, are for reference indicators. These DNA fragments were...

  • 6 X DNA loading Dye is useful for loading DNA samples into wells on agrarose gel electrophoresis. It contains EDTA, glycerol, bromphenol blue and 10 mM Tris-HCl (pH8.0).

  • E.coli harboring the plasmid encoding the gene of alkaline phosphatase from Shewanella sp. SIB1 (PAP).

  • Taq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. The enzyme has proven to have high amplification yield, be stable at high temparetaure.

  • Taq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. The enzyme has proven to have high amplification yield, be stable at high temparetaure.

  • Taq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. The enzyme has proven to have high amplification yield, be stable at high temparetaure.

  • HotTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3' - 5'exonuclease activity. Prior the first PCR step the HotTaq DNA polymerase should be activated by 15 minute incubation at 95-97ºC.

  • HotTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3' - 5'exonuclease activity. Prior the first PCR step the HotTaq DNA polymerase should be activated by 15 minute incubation at 95-97ºC.

  • HotTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3' - 5'exonuclease activity. Prior the first PCR step the HotTaq DNA polymerase should be activated by 15 minute incubation at 95-97ºC.

  • RedTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. The enzyme has proven to have high amplification yield, be stable at high temparetaure. Added inert dye will not have any interference to the reaction. Visual confirmation that the enzyme has been added and proper component mixing...

Mostrando 1 - 12 de 31638 items