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Merck

11363514910

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

Synonim(y):

luminescent detection kit

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Wybierz wielkość

50 TESTS
4060,00 zł

4060,00 zł


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Wybierz wielkość

Zmień widok
50 TESTS
4060,00 zł

About This Item

Kod UNSPSC:
41116134

4060,00 zł


Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności

Próba

>98% (NMR)

Poziom jakości

zastosowanie

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

opakowanie

kit of 1 (5 components)

producent / nazwa handlowa

Roche

charakterystyka ekologicznej alternatywy

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

sustainability

Greener Alternative Product

metody

hybridization: suitable

kategoria ekologicznej alternatywy

temp. przechowywania

−20°C

Opis ogólny

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.

Zastosowanie

DIG Luminescent Detection Kit has been used for highly sensitive and specific detection of DIG-labeled nucleic acids in:
  • critical commercial assays[1]
  • Southern hybridization[2][3]
  • northern analysis[4]
  • plaque or colony lifts with anti-DIG-AP conjugate and the chemiluminescent substrate CSPD[2][4]. Chemiluminescent detection with CSPD (following the instructions of the kit) is as sensitive as radioactive methods, but requires much shorter exposure times.

Opakowanie

1 kit containing 5 components.

Charakterystyka techniczna

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.

Uwaga dotycząca przygotowania

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.

Inne uwagi

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

Numer produktu
Opis

  • 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

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

does not flashNot applicable

Temperatura zapłonu (°C)

does not flashNot applicable


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Dongqing Huang et al.
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
Karl Dichtl et al.
Molecular microbiology, 95(3), 458-471 (2014-11-27)
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
Jes-Niels Boeckel et al.
Circulation research, 117(10), 884-890 (2015-09-18)
Circular RNAs (circRNAs) are noncoding RNAs generated by back splicing. Back splicing has been considered a rare event, but recent studies suggest that circRNAs are widely expressed. However, the expression, regulation, and function of circRNAs in vascular cells is still
Circ-ZNF609 is a circular RNA that can be translated and functions in myogenesis.
Legnini I, et al.
Molecular Cell, 66(1), 22-37 (2017)
Fang Zheng et al.
Nature communications, 12(1), 1341-1341 (2021-02-28)
Hypoxia-inducible factor-1 (HIF-1) is a master driver of glucose metabolism in cancer cells. Here, we demonstrate that a HIF-1α anti-sense lncRNA, HIFAL, is essential for maintaining and enhancing HIF-1α-mediated transactivation and glycolysis. Mechanistically, HIFAL recruits prolyl hydroxylase 3 (PHD3) to

Produkty

Metody znakowania digoksygeniną (DIG) i zestawy do sond DNA i RNA DIG, znakowanie DNA z losowym primerem, znakowanie nickiem translacyjnym, znakowanie końcowe oligonukleotydów 5' i 3'.

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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