Przejdź do zawartości
Merck

AMPD1

Sigma-Aldrich

DNase I

Amplification Grade

Synonim(y):

Deoxyribonuclease I

Zaloguj sięWyświetlanie cen organizacyjnych i kontraktowych


About This Item

Numer EC enzymu:
Kod UNSPSC:
41106300
NACRES:
NA.55

Poziom jakości

Postać

liquid

stężenie

1 unit/μL

metody

RT-PCR: suitable

kolor

colorless

Warunki transportu

wet ice

temp. przechowywania

−20°C

Opis ogólny

Deoxyribonuclease I (DNase I) is an endonuclease isolated from bovine pancreas that digests double and single stranded DNA into oligo and mononucleotides. Amplification Grade DNase I has been purified to remove RNase activity, and is suitable for eliminating DNA from RNA preparations prior to sensitive applications, such as RT-PCR (Reverse Transcriptase - Polymerase Chain Reaction).

DNase I digests double- and single-stranded DNA into oligo- and mononucleotides. Using the Reaction Buffer provided, DNA is removed from RNA preparations in a 15 minute digestion at room temperature. The DNase I is then inactivated by heating with the Stop Solution. Heating also denatures hairpins in the RNA, so the RNA can be used directly in reverse transcription.

No current RNA isolation procedure removes 100% of the DNA. Many commercial DNase I formulations are contaminated with residual RNases. This RNase contamination can destroy or degrade valuable RNA samples prior to reverse transcription. Laboratory comparisons have shown that Sigma′s Amplification Grade DNase I demonstrates lower RNase activity than that from several leading molecular biology product suppliers.

Zastosowanie

Amplification grade DNase I has been used:
  • for the digestion of DNA during isolation and purification of RNA. The purified RNA can be used for the synthesis of cDNA using RNA reverse transcriptase.
  • to hydrolyze extracellular matrix (ECM) components and enhance photosensitizer penetration into the biofilm to determine the efficacy of antimicrobial photodynamic therapy (aPDT) on Candida albicans biofilms
  • to remove contaminating DNA from total RNA extracted from cattle blood samples

Cechy i korzyści

  • Suitable for the elimination of DNA from RNA
  • Minimal RNase activity available
  • Optimized 10× reaction buffer and Stop Solution for complete inactivation of DNase I

Przydatność

Suitable for use in removing DNA from RNA preparations.

Definicja jednostki

One unit completely digests 1 μg of plasmid DNA to oligonucleotides in 10 min. at 37 °C.

Informacje prawne

Purchase of this product is accompanied by a limited license for use in the Polymerase Chain Reaction (PCR) process for research purposes only and in conjunction with a thermal cycler whose use in the automated performance of the PCR process is covered by an up-front license fee, either by payment to Applied Biosystems or as purchased, i.e., and authorized thermal cycler.
This page may contain text that has been machine translated.

Kod klasy składowania

10 - Combustible liquids

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

Masz już ten produkt?

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

Odwiedź Bibliotekę dokumentów

Leonie Doorduin et al.
DNA research : an international journal for rapid publication of reports on genes and genomes, 18(2), 93-105 (2011-03-30)
Invasive individuals from the pest species Jacobaea vulgaris show different allocation patterns in defence and growth compared with native individuals. To examine if these changes are caused by fast evolution, it is necessary to identify native source populations and compare
Xian-Jun Liang et al.
Molecular vision, 18, 1649-1657 (2012-07-10)
Vascular endothelial growth factor (VEGF) is the most potent angiogenic mitogen, and has been associated with angiogenesis. Heparanase is an endoglycosidase that specifically cleaves heparan sulfate side chains, which can induce VEGF expression. The aims of the present study were
Rahel D May et al.
Neurospine, 17(1), 77-87 (2020-04-07)
Spinal fusion surgery is a common treatment modality for various pathologic conditions of the spine. The bone morphogenetic protein 2 (BMP2) analogue L51P acts as a general inhibitor of BMP antagonists, whereas it shows a weak affinity for BMP type
Hafid Ait-Oufella et al.
The Journal of experimental medicine, 207(8), 1579-1587 (2010-07-07)
B cell depletion significantly reduces the burden of several immune-mediated diseases. However, B cell activation has been until now associated with a protection against atherosclerosis, suggesting that B cell-depleting therapies would enhance cardiovascular risk. We unexpectedly show that mature B
John P Dunbar et al.
Toxins, 12(6) (2020-06-24)
The noble false widow spider Steatoda nobilis originates from the Macaronesian archipelago and has expanded its range globally. Outside of its natural range, it may have a negative impact on native wildlife, and in temperate regions it lives in synanthropic

Produkty

Zastosowanie oligos modyfikowanych lipidami MULTI-seq, protokół i przewodnik rozwiązywania problemów dla testów PCR i aplikacji sekwencjonowania.

Protokoły

Method for reverse transcription of RNA into DNA. Uses a premixed reagent that contains reverse transcriptase, dNTPs, primers, RNase inhibitor and buffer. Fast generation of cDNA.

The SeqPlex RNA Amplification kit provides a method for amplification of total RNA or isolated mRNA prior to entry into the workflows of the commonly used deep sequencing platforms.

Powiązane treści

Spectrum Plant Total RNA Kit oczyszcza RNA z trudnych gatunków i tkanek za pomocą zgłoszonej do opatentowania chemii.

Polymerase chain reaction (PCR) is a technique for amplifying nucleic acid molecules and is commonly used in many applications, including RT-PCR, hot start PCR, end point PCR and more.

Reakcja łańcuchowa polimerazy (PCR) jest techniką amplifikacji cząsteczek kwasów nukleinowych i jest powszechnie stosowana w wielu aplikacjach, w tym RT-PCR, hot start PCR, end point PCR i innych.

Reakcja łańcuchowa polimerazy (PCR) jest techniką amplifikacji cząsteczek kwasów nukleinowych i jest powszechnie stosowana w wielu aplikacjach, w tym RT-PCR, hot start PCR, end point PCR i innych.

Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.

Skontaktuj się z zespołem ds. pomocy technicznej