Roche Dnase I

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Roche Dnase I
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  • …Recombinant DNase I is a DNA-specific endonuclease.The enzyme catalyzes the degradation of both double- and single-stranded DNA randomly by hydrolyzing phosphodiester linkages to DNA, resulting in a mixture of oligo- and mononucleotides. All material used during the production process of DNase I

  • …cause clumping of cells. Addition of DNase I to the dissociation buffer leads to a degradation of this extracellular DNA, therby avoiding the loss of cells from undesired clumping. General description: Bovine pancreatic deoxyribonuclease I (DNase I) is a DNA minor grove-interacting…

  • …deoxyribonuclease I (DNase I) has been used for- • The isolation of cells from lung, skin and tumor samples Bacterial DNA extraction from live bacterial cells that are resistant to DNase I † General description: Bovine pancreatic deoxyribonuclease I (DNase I) is a DNA…

  • …Mg 2+ DNase I causes single-stranded nicks in dsDNA, while in the presence of Mn 2+ the enzyme produces double-stranded breaks. Storage conditions (working solution): Long-term Storage of the Dissolved Enzyme The solvent generally recommended for DNase I is water. When DNase I is reconstituted…

  • …spermidine) Storage conditions (working solution): Solution is stable to at least 12 months if stored at 2 to 8 °C, contact with DNase or bacteria is to avoid. Sequence: In an aqueous solution the DNA itself is a salt (the acid groups of the phosphate back bone have a negative…

  • …glycerol (v/v), DNA Polymerase I and DNase I. Specificity: Heat inactivation: Stop the reaction by adding 1 μl 0.5 M EDTA (pH 8.0) and heating to 65 °C for 10 minutes. Principle: The nick translation method is based on the ability of DNase I to introduce randomly distributed…

  • …μl 0.4 mM; dTTP, 50 μl 0.4 mM; Nick Translation Buffer, 100 μl 10x concentrated; Enzyme Mixture, 100 μl, DNA Polymerase I and DNase I in 50% glycerol (v/v) RIDADR: NONH for all modes of transport Application: The kit is used for labeling of DNA with radioactive or modified…

  • MilliporeSigma

    …is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patent claims require a separate license from Roche. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems,…

  • …ATP, in Tris buffer 10 mM; CTP, in Tris buffer 10 mM; GTP, in Tris buffer 10 mM; UTP, in Tris buffer 10 mM; Transcription Buffer 10x concentrated; DNase I, RNase free, in buffer with 50% glycerol; RNase Inhibitor, in buffer with 50% glycerol; SP6 RNA Polymerase, in buffer with 50% glycerol; T7 RNA…

  • …Polymerase 20 U/μl; T7 RNA Polymerase 20 U/μl; T3 RNA Polymerase 20 U/μl; Anti-Digoxigenin-AP antibody, Fab fragments 750 U/ml; DNase I, RNase free 10 U/μl; CDP- Star ready-to-use; Actin RNA Probe, DIG-labeled Antisense Probe, length 588 bases 10 ng/μl; DIG Easy Hyb…

  • …0.2 and 15 kb in: Analysis of PCR products • Examination of restriction endonucleases • Digests of plasmid, cosmid, and λ phage DNA • Electrophoresis of RNA in, e.g. , denaturing gels containing formaldehyde Nucleic acid fragments separated with Agarose LE…

  • …no amplification product is obtained. Components: • Lysis/Binding Buffer • DNase I, lyophilizate • DNase Incubation Buffer • Wash Buffer I • Wash Buffer II • Elution Buffer • High Pure Spin Filter Tubes (containing…

  • …digested with DNase I directly on the filter. Brief wash-and-spin steps readily remove the digested DNA fragments and other contaminating substances. The remaining purified RNA is then eluted in a small volume of low-salt buffer. Legal Information: LightCycler is a registered trademark of Roche

  • …from the column, residual DNA is digested by incubating the eluate with DNase I. A second incubation step with Proteinase K improves the purity of RNA. Finally, a low-salt elution releases the RNA from the glass fiber fleece. Legal Information: LightCycler is a registered trademark of Roche

  • …on native proteins and can therefore be used to rapidly inactivate endogenous nucleases such as RNases and DNases. The enzyme is also available as a solution. • I nhibitors : The enzyme is inactivated by Pefabloc ® SC. However, it is not inactivated by metal ions, chelating…

  • Roche Applied Science.For nonradioactive labeling of in situ probes with other haptens, Roche Applied Science offers the DIG-Nick Translation Mix or the Nick Translation Mix. Physical form: 1 vial with 5x concentrated stabilized reaction buffer in 50% glycerol (v/v) and DNA Polymerase I, DNase I,

  • MilliporeSigma

    …from Roche Applied Science. For nonradioactive labeling of in situ probes with other haptens and fluorophores, Roche Applied Science offers the Biotin-Nick Translation Mix and the Nick Translation Mix (without nucleotides). Principle: The nick translation method is based on the ability of DNase I

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