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Roche

DIG Luminescent Detection Kit

greener alternative

sufficient for 50 blots (10 cm x 10 cm each), kit of 1 (5 components), suitable for hybridization

Synonym(s):

luminescent detection kit

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About This Item

UNSPSC Code:
41116134

Assay

>98% (NMR)

Quality Level

usage

sufficient for 50 blots (10 cm x 10 cm each)

packaging

kit of 1 (5 components)

manufacturer/tradename

Roche

greener alternative product characteristics

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

sustainability

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technique(s)

hybridization: suitable

greener alternative category

storage temp.

−20°C

General description

DIG Luminescent Detection Kit is used for the detection of digoxigenin-labeled nucleic acids by enzyme immunoassay with luminescence on nylon membranes. The nonradioactive DIG system uses digoxigenin, a steroid hapten, coupled to deoxyuridine triphosphate (dUTP), UTP or didUTP to label DNA, RNA or oligonucleotides for hybridization and subsequent luminescent detection.
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 using 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.

Application

DIG Luminescent Detection Kit has been used for highly sensitive and specific detection of DIG-labeled nucleic acids in:
  • critical commercial assays
  • Southern hybridization
  • northern analysis
  • plaque or colony lifts with anti-DIG-AP conjugate and the chemiluminescent substrate CSPD. Chemiluminescent detection with CSPD (following the instructions of the kit) is as sensitive as radioactive methods, but requires much shorter exposure times.

Packaging

1 kit containing 5 components.

Specifications

Sensitivity: 0.03 pg of homologous DNA or 0.1 pg of homologous RNA is detected in a Southern or dot blot after <30-min exposure time. Single-copy genes are detected in 0.3 μg mammalian genomic DNA.

Preparation Note

Working concentration: 0.5mg/ml for flow cytometry
  • Storage conditions (working solution): Antibody conjugate (vial 3): once opened, should be stored at 2 to 8°C
  • Blocking Reagent (bottle 4): in solution at 2 to 8°C
  • CSPD (vial 5): at 2 to 8°C when frequently used. Repeated freeze/thaw cycles should be avoided.

Enzymatic dephosphorylation of the dioxetane CSPD by alkaline phosphatase leads to the metastable phenolate anion, which decomposes and emits light at 477nm. The light emission increases with time until a constant intensity is attained.
Assay Time
  • Immunological detection 1.5 hours
  • Signal detection 5 to 30 minute

Note: Store protected from light.

Other Notes

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

Kit Components Only

Product No.
Description

  • DIG-labeled Control DNA 5 µg/ml

  • DNA Dilution Buffer

  • Anti-digoxigenin-AP antibody, Fab fragments 750 U/ml

  • Blocking Reagent

  • CSPD 11.6 mg/ml

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

does not flashNot applicable

Flash Point(C)

does not flashNot applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Karl Dichtl et al.
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Echinocandins inhibit β-1,3-glucan synthesis and are one of the few antimycotic drug classes effective against Aspergillus spp. In this study, we characterized the β-1,3-glucan synthase Fks1 of Aspergillus fumigatus, the putative target of echinocandins. Data obtained with a conditional mutant
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Genetics, 203(1), 353-368 (2016-03-28)
In response to replication stress, a phospho-signaling cascade is activated and required for coordination of DNA repair and replication of damaged templates (intra-S-phase checkpoint) . How phospho-signaling coordinates the DNA replication stress response is largely unknown. We employed state-of-the-art liquid
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DNA Replication Stress Phosphoproteome Profiles Reveal Novel Functional Phosphorylation Sites on Xrs2 in Saccharomyces cerevisiae.
Huang D, et al.
Genetics, 203(1), 353-368 (2016)

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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