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11 results for Nucleic Acid Modification and Labelling | Avantor

Nucleic Acid Modification and Labelling

Nucleic acid reagents form the foundation of genetic analysis and molecular biology, playing a pivotal role from cloning to gene expression studies. Delve into our collection featuring high-fidelity enzymes for end-point PCR, advanced reagents for isothermal amplification, and comprehensive kits for nucleic acid purification. For precision in quantitative assays, explore our selection of qPCR and RT-qPCR kits, primed for unparalleled accuracy. Our portfolio also includes next-generation sequencing reagents, offering cutting-edge solutions for genomic sequencing and personalized medicine advancements.

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Oligonucleotide Conjugation Kit, Abcam

Supplier: Abcam

Abcam's Oligonucleotide Conjugation Kit (ab218260) offers several standout features: - Rapid Conjugation: enables generation of antibody-oligonucleotide conjugates in less than 2 hours. - High Efficiency: achieves high levels of antibody and oligonucleotide recovery, with conjugation efficiency ~ 95-100%. - Versatility: Suitable for conjugating antibodies to single-stranded oligonucleotides (10-120 bases) and double-stranded oligonucleotides (up to 80 bases), providing flexibility for various research needs

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T4 DNA polymerase

T4 DNA polymerase

Supplier: Thermo Fisher Scientific

T4 DNA Polymerase catalyses the 5'→3' synthesis of DNA from a primed single-stranded DNA template.

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SAVIEW® PLUS HRP Reagent

Supplier: Enzo Life Sciences

High sensitivity, low background streptavidin-based nanopolymer detection reagent for use with HIGHDEF® chromogens in ISH and IHC applications.

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T4 UvsX DNA Recombinase

Supplier: G-Biosciences

T4 UvsX DNA recombinase mediates DNA strand exchange between homologous chromosomes. The protein forms a right-handed nucleoprotein complex on single ssDNA called the presynaptic filament that can search for homology in duplex DNA and pair the recombining DNA molecules to form a DNA joint molecule. This process is aided by ssDNA binding proteins and recombination mediators. The filament is then elongated by DNA polymerase with the newly synthesised strand displacing the old strand. The newly synthesised duplex DNA can then act as a template for the next cycle to achieve exponential amplification of dsDNA. E.coli cells expressing recombinant T4 UvsX gene.

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PCR decontamination kit

Supplier: Enzo Life Sciences

Rapid removal of contaminating DNA in PCR mastermixes, without reduction in PCR sensitivity.

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ReadiView™ Blue Real-Time PCR Visualisation Dye *200X*

ReadiView™ Blue Real-Time PCR Visualisation Dye *200X*

Supplier: AAT Bioquest

ReadiView™ Blue Real-Time PCR Visualisation Dye is a 200X concentrated, ready-to-use, inert dye that enhances the visibility of real-time PCR reactions for more accurate pipetting and plate loading.

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Phusion® site-directed mutagenesis kit

Phusion® site-directed mutagenesis kit

Supplier: FINNZYMES REAGENTS

Phusion® Site-Directed Mutagenesis Kit is a versatile and efficient tool for introducing point mutations, insertions, or deletions in any type of plasmid DNA.

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Amplite® Tyramide (TSA) UV Channel Signal Scavenger *10X*

Amplite® Tyramide (TSA) UV Channel Signal Scavenger *10X*

Supplier: AAT Bioquest

Tyramide signal amplification (TSA) is a technique used to enhance the signal of target molecules, such as antibodies or nucleic acid probes.

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Amplite® Tyramide (TSA) Signal Booster

Amplite® Tyramide (TSA) Signal Booster

Supplier: AAT Bioquest

Tyramide signal amplification (TSA) is a technique used to enhance the signal of target molecules, such as antibodies or nucleic acid probes, in immunohistochemistry and in situ hybridisation.

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Hybrisol VII

Supplier: MP Biomedicals

Hybrisol VII

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ABE8e Adenine Base Editor

Supplier: Genscript

ABE8e is an innovative adenine base editor designed to enable precise genetic modifications by converting A-T base pairs to G-C base pairs without introducing double-stranded breaks or requiring donor DNA templates.​ABE8e contains eight additional mutations in the TadA domain, augments the effectiveness and applicability of adenine base editing.

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