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Roche

Random Primed DNA Labeling Kit

Synonym(s):

nucleic acid labeling

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About This Item

UNSPSC Code:
41105500

usage

sufficient for 50 labeling reactions

Quality Level

manufacturer/tradename

Roche

storage temp.

−20°C

Related Categories

General description

Random primed DNA labeling kit is used for the radioactive and nonradioactive labeling of DNA with modified deoxyribonucleoside triphosphate using random oligonucleotides as primers. In this method, the complementary DNA strand of denatured DNA is synthesized by Klenow polymerase using the 3′-OH termini of the random oligonucleotides as primers.

Specificity

Heat inactivation: Stop the reaction by adding 2 μl 0.2 M EDTA (pH 8.0) and/or by heating to 65 °C for 10 minutes.

Application

Random Primed DNA Labeling Kit has been used to label probe or fragments shorter than 1 kb.
Random Primed DNA Labeling Kit is used to uniformly label plasmid or phage DNA with any [α-32P]-dNTP or modified dNTP. Labeled DNA probes with high specific activity are used in a variety of hybridization techniques including:
  • Screening of gene libraries
  • Southern, dot and northern blots
  • In situ hybridizations

Packaging

1 kit containing 7 components.

Preparation Note

Working solution: Preparation dNTP Stock Mix
To avoid pipetting inaccuracy, due to low volumes, prepare a stock mix of unlabeled dNTPs. Aliquots should be stored at -15 to -25 °C. Avoid repeated freezing and thawing.
  • dATP, dGTP, dTTP mixture:
    For one labeling reaction pipette:
    1 μl dATP
    1 μl dGTP
    1 μl dTTP to a reaction vial

Preparation of DIG Stock Mix
To avoid pipetting inaccuracy due to low volumes, prepare a DIG stock mix. To do this, mix digoxigenin-11-dUTP [3 mM] and dTTP (vial 5) 1:1. For each labeling reaction 1.6 μl are used.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Kit Components Only

Product No.
Description

  • Control DNA lambda, 20 μl 12.5 µg/ml

  • dATP, 50 μl 0.5 mM

  • dCTP, 50 μl 0.5 mM

  • dGTP, 50 μl 0.5 mM

  • dTTP, 50 μl 0.5 mM

  • Hexanucleotide mixture in 10x reaction buffer (100 μl)

  • Klenow enzyme, labeling grade (100 U)

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_f

does not flash

flash_point_c

does not flash


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I J Blader et al.
The Journal of biological chemistry, 276(26), 24223-24231 (2001-04-11)
Cells infected with the intracellular protozoan parasite Toxoplasma gondii undergo up-regulation of pro-inflammatory cytokines, organelle redistribution, and protection from apoptosis. To examine the molecular basis of these and other changes, gene expression profiles of human foreskin fibroblasts infected with Toxoplasma
Fluorescence in situ hybridization to the polytene chromosomes of anopheles mosquitoes
He F, et al.
PLoS Pathogens (2012)
Daniel R Semlow et al.
Cell, 167(2), 498-511 (2016-10-04)
During eukaryotic DNA interstrand cross-link (ICL) repair, cross-links are resolved ("unhooked") by nucleolytic incisions surrounding the lesion. In vertebrates, ICL repair is triggered when replication forks collide with the lesion, leading to FANCI-FANCD2-dependent unhooking and formation of a double-strand break
Margit Dlaska et al.
Cell cycle (Georgetown, Tex.), 12(13), 2084-2099 (2013-06-14)
Immortal cells require a mechanism of telomere length control in order to divide infinitely. One mechanism is telomerase, an enzyme that compensates the loss of telomeric DNA. The second mechanism is the alternative lengthening of telomeres (ALT) pathway. In ALT
Masayuki Kimura et al.
Nature protocols, 5(9), 1596-1607 (2010-11-19)
In this protocol we describe a method to obtain telomere length parameters using Southern blots of terminal restriction fragments (TRFs). We use this approach primarily for epidemiological studies that examine leukocyte telomere length. However, the method can be adapted for

Protocols

Random Primed DNA Labeling Kit Protocol & Troubleshooting

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