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Merck

11745808910

Roche

Nick Translation Mix

sufficient for 50 labeling reactions, pkg of 200 μL, solution

Sinónimos:

nick translation

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About This Item

Código UNSPSC:
41105500

formulario

solution

Nivel de calidad

uso

sufficient for 50 labeling reactions

envase

pkg of 200 μL

fabricante / nombre comercial

Roche

técnicas

nucleic acid labeling: suitable

color

colorless

pH

~7.5 (68 °F)

solubilidad

water: miscible

idoneidad

suitable for fluorescent labeling techniques
suitable for molecular biology

aplicaciones

genomic analysis
life science and biopharma

temp. de almacenamiento

−20°C

Descripción general

Optimized enzyme mixture: Nick translation utilizes a combination of DNase and DNA Polymerase to nick one strand of the DNA helix, then incorporates labeled nucleotides as the polymerase examines, or "proofreads" the nicked site.
Individual templates produce consistent results in the standard 90-minutes reaction, and result in an average probe length of 200 base pairs up to 500 base pairs.
Assay Time: 100 minutes

Sample Materials

  • Supercoiled and linearized plasmid DNA
  • Supercoiled and linearized cosmid DNA
  • Purified PCR products

Especificidad

Heat inactivation: Stop the reaction by adding 1 μl 0.5 M EDTA (pH 8.0) and heating to 65 °C for 10 minutes.

Aplicación

For generation of highly sensitive probes for fluorescence in situ hybridization (FISH).
The Nick Translation Mix is designed for direct fluorophore-labeling of in situ probes. Fluorescein-12-dUTP and Tetramethyl-Rhodamine-5-dUTP from Roche Applied Science or other commercially available fluorophor-labeled nucleotides can be combined with the Nick Translation Mix. Direct fluorophore-labeled in situ probes are used for the detection of multi copy or very large hybridization targets on metaphase chromsomes or interphase nuclei.
For a standard labeling reaction using 1 μg template in 20 μl total reaction volume, 4 μl of 5x concentrated fluorophore labeling mix are required.

Componentes

Contents

1 vial with 5x concentrated solution, stabilized reaction buffer in 50% glycerol (v/v), DNA Polymerase I and DNase I.

Calidad

Function tested in dot spot assay.

Principio

The nick translation method is based on the ability of DNase I to introduce randomly distributed nicks into DNA at low enzyme concentrations in the presence of MgCl2.
E. coli DNA Polymerase I synthesizes DNA complementary to the intact strand in a 5′?3′ direction using the 3′-OH termini of the nick as a primer. The 5′?3′ exonucleolytic activity of DNA polymerase I simultaneously removes nucleotides in the direction of synthesis. The polymerase activity sequentially replaces the removed nucleotides with isotope-labeled or hapten-labeled deoxyribonucleoside triphosphates. At low temperature (+15°C), the unlabeled DNA in the reaction is thus replaced by newly synthesized labeled DNA.

Almacenamiento y estabilidad

Avoid repeated freezing and thawing.

Otras notas

For life science research only. Not for use in diagnostic procedures.
Denaturing of the template before nick translation is not required.

Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

does not flash

Punto de inflamabilidad (°C)

does not flash


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