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Roche

DIG DNA Labeling and Detection Kit

greener alternative

Synonym(s):

dna labeling and detection kit, dig

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About This Item

UNSPSC Code:
41105500

usage

sufficient for 25 labeling reactions
sufficient for 50 blots

Quality Level

manufacturer/tradename

Roche

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

greener alternative category

storage temp.

−20°C

General description

DIG DNA Labeling and Detection Kit is a convenient kit for random-primed labeling of DNA with digoxigenin-deoxyuridine triphosphate (dUTP), alkali-labile and color detection of hybrids by enzyme immunoassay. In this method, the complementary strand of denatured DNA is synthesized by Klenow polymerase using the 3′-OH termini of random oligonucleotides as primers.

Contents:
  • Unlabeled Control DNA 1, 100 μg/ml
  • Unlabeled Control DNA 2, 200 μg/ml
  • DNA Dilution Buffer
  • DIG-labeled Control DNA, 5.2 μg/ml
  • 10x Hexanucleotide Mix
  • 10x dNTP Labeling Mixture
  • Klenow Enzyme, Labeling grade, 2 U/μl
  • Anti-digoxigenin-AP-conjugate, 750 U/ml
  • NBT/BCIP Concentrated Stock Solution
  • Blocking Reagent
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is designed as a safer chemical. The DIG System was established as a sensitive and cost-effective alternative to radioactivity for the labeling and detection of nucleic acids. There are many available publications that prove the versatility of the DIG System, so use of radio-labeling is no longer the only option for labeling of DNA for hybridization.

Specificity

Sensitivity and specificity: The standard labeling reaction with 1 μg template will give a yield of 260 ng DIG-labeled DNA after a 1-hour incubation at +37°C, or 780 ng after a 20-hour incubation. The sensitivity of DIG detection depends on the concentration of the DIG-labeled probe in the hybridization reaction, and the duration of the color reaction.

Application

DIG DNA Labeling and Detection Kit has been used in a variety of hybridization techniques:
  • Southern blots
  • Northern blots
  • Dot blots
  • Colony and plaque screening
DIG-labeled hybrids are detected with an anti-DIG-alkaline phosphatase conjugate and the substrates NBT (nitroblue tetrazolium salt) and BCIP (5-bromo-4-chloro-3-indolyl phosphate, toluidinium salt), which give a light blue precipitate.

Packaging

1 kit containing 10 components.

Preparation Note

Working concentration: Dilution of Antibody 1:5,000

Other Notes

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

Kit Components Only

Product No.
Description

  • Unlabeled Control DNA 1 100 µg/ml

  • Unlabeled Control DNA 2 200 µg/ml

  • DNA Dilution Buffer

  • DIG-labeled Control DNA 5.2 µg/ml

  • Hexanucleotide Mix 10x concentrated

  • dNTP Labeling Mixture 10x concentrated

  • Klenow Enzyme, Labeling grade 2 U/µl

  • Anti-digoxigenin-AP-conjugate antibody 750 U/ml

  • NBT/BCIP Concentrated Stock Solution

  • Blocking Reagent

See All (10)

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

does not flashNot applicable

Flash Point(C)

does not flashNot applicable


Certificates of Analysis (COA)

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Scientific reports, 8(1), 593-593 (2018-01-14)
CRISPR/Cas9-based genome editing has dramatically accelerated genome engineering. An important aspect of genome engineering is efficient knock-in technology. For improved knock-in efficiency, the non-homologous end joining (NHEJ) repair pathway has been used over the homology-dependent repair pathway, but there remains
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In early mammalian embryos, it remains unclear how the first cell fate bias is initially triggered and amplified toward cell fate segregation. Here, we report that a long noncoding RNA, LincGET, is transiently and asymmetrically expressed in the nucleus of
Diana C Garcia-Ramon et al.
Microbial biotechnology, 11(2), 302-316 (2017-10-14)
Bacillus pumilus strain 15.1 was previously found to cause larval mortality in the Med-fly Ceratitis capitata and was shown to produce crystals in association with the spore. As parasporal crystals are well-known as invertebrate-active toxins in entomopathogenic bacteria such as
Handeng Liu et al.
Journal of invertebrate pathology, 99(2), 235-238 (2008-07-22)
Among Microsporidia, Nosema bombycis has a novel arrangement of LSUrRNA, SSUrRNA, ITS, IGS and 5SrRNA. To determine the distribution of rDNA among the chromosomes, we performed genome-wide screening and Southern blotting with three probes (SSU, ITS and IGS). Southern blotting
Nasser Shakhssalim et al.
Cancer cell international, 13(1), 120-120 (2013-12-07)
Bladder cancer is a relatively common and potentially life-threatening neoplasm that ranks ninth in terms of worldwide cancer incidence. The aim of this study was to determine deletions and sequence variations in the mitochondrial displacement loop (D-loop) region from the

Articles

Digoxigenin (DIG) labeling methods and kits for DNA and RNA DIG probes, random primed DNA labeling, nick translation labeling, 5’ and 3’ oligonucleotide end-labeling.

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