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T3809

Sigma-Aldrich

TRI-Reagenz®

BD, For processing whole blood, plasma, or serum.

Synonym(e):

TRI Reagent® RNA Isolations Reagens

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25 ML
CHF 85.70
100 ML
CHF 268.00
200 ML
CHF 475.00

CHF 85.70


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Größe auswählen

Ansicht ändern
25 ML
CHF 85.70
100 ML
CHF 268.00
200 ML
CHF 475.00

About This Item

MDL-Nummer:
UNSPSC-Code:
12352200
NACRES:
NA.52

CHF 85.70


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Qualitätsniveau

Verwendung

0.75 mL sufficient for 0.25 mL blood derivatives

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Allgemeine Beschreibung

TRI Reagent BD is a quick and convenient reagent for use in the simultaneous isolation of RNA, DNA and protein from serum, plasma or whole blood. A convenient single-step liquid phase separation results in the simultaneous isolation of RNA, DNA and protein. This procedure is an adaptation of the single-step method reported by Chomczynski and Sacchi for total RNA isolation, and permits fast and efficient processing of blood derivatives.

TRI REAGENT BD performs well with large or small sample volumes, and many samples can be simultaneously extracted. TRI Reagent BD is a mixture of guanidine thiocyanate and phenol in a mono-phase solution. When a sample of blood derivatives is lysed with it, and chloroform or 1-bromo-3-chloropropane is added, the mixture separates into 3 phases: an aqueous phase containing the RNA, the interphase containing DNA and an organic phase containing proteins. Each component can then be isolated after separating the phases. 0.75 ml of TRI REAGENT BD processes 0.25 ml of blood derivatives.

This is one of the most effective methods for isolating total RNA and can be completed in only 1 hour starting with fresh cells. The procedure is very effective for isolating RNA molecules of all types from 0.1 to 15 kb in length. The resulting RNA is intact with little or no contaminating DNA or protein.
TRI Reagent® is a monophasic solution of phenol and guanidinium isothiocyanate.[1]

Anwendung

TRI-Reagenz ist eine verbesserte Version des von Chomczynski entwickelten einstufigen Gesamt-RNA-Isolationsreagenzes. Die auf diesem Reagenz basierende RNA-Isolierungsmethode ist für RNA-Anwendungen weit verbreitet und bewährt. Es eignet sich besonders für die schnelle, kostengünstige und effiziente Isolation von Gesamt-RNA oder die gleichzeitige Isolierung von RNA, DNA und Proteinen aus Proben menschlichen, tierischen, pflanzlichen, Hefe-, bakteriellen und viralen Ursprungs.
TRI Reagent® has been used for the isolation of RNA.[2][3]
The resulting RNA can be used for Northern blots, mRNA isolation, in vitro translation, RNase protection assays, cloning and PCR.

Leistungsmerkmale und Vorteile

  • Leicht skalierbare RNA-Isolation
  • Vielseitig einsetzbar mit: Menschen, Pflanzen, Hefe, Bakterien oder Viren
  • Bessere Erträge als traditionelle Guanidinthiocyanat/Cäsiumchlorid-Methoden

Rechtliche Hinweise

TRI Reagent is a registered trademark of Molecular Research Center, Inc.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B - STOT RE 2

Zielorgane

Nervous system,Kidney,Liver,Skin

Zusätzliche Gefahrenhinweise

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flammpunkt (°F)

174.2 °F - closed cup

Flammpunkt (°C)

79 °C - closed cup


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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Heiner Kuhl et al.
Molecular biology and evolution, 38(1), 108-127 (2020-08-12)
Presumably, due to a rapid early diversification, major parts of the higher-level phylogeny of birds are still resolved controversially in different analyses or are considered unresolvable. To address this problem, we produced an avian tree of life, which includes molecular
A novel CLCN5 mutation in a Chinese boy with Dent's disease.
Ji LN
World Journal of Pediatrics : WJP, 10(3), 275-277 (2014)
Circulating ribonucleic acids and metabolic stress parameters may reflect progression of autoimmune or inflammatory conditions in juvenile type 1 diabetes.
Kocic G
TheScientificWorldJournal, 11, 1496-1508 (2011)
John-Edwin Thomson et al.
Pancreas, 48(1), 107-112 (2018-11-20)
Interleukin-21 (IL-21) is a cytokine associated with tissue inflammation, autoimmune and infectious diseases. Organ dysfunction and death can occur in patients with acute pancreatitis (AP) in two distinct clinical phases. Initially, a systemic inflammatory response syndrome may be followed by
Purification of RNA using TRIzol (TRI reagent)
Rio D, et al.
Cold Spring Harbor Protocols, 2010(6), pdb-prot5439 (2010)

Artikel

Simple DNA/RNA purification methods aid genome analysis from various sources, enhancing research efficiency.

Die Verfügbarkeit von einfachen Verfahren zum Aufreinigen von DNA und RNA hat die Analyse und Charakterisierung des Genoms und der Genexpression in hohem Maß erleichtert. Es besteht eine Anforderung, DNA und RNA schnell und praktisch aus verschiedenen zellulären Quellen, einschließlich Gewebe aus Tier-, Pflanzen- und Bakterienkulturen, zu isolieren.

Questions

  1. When using Tri Reagent BD, do we need to add EDTA to blood samples to prevent coagulation?

    1 answer
    1. The Product Information available under More Documents or at this link (https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/436/845/t3809bul.pdf) provides the following instructions:

      I. Sample Preparation:

      1A. Serum: Add 0.25 ml of serum to 0.75 ml of TRI Reagent BD. Close the tube and shake the solution by hand or vortex, ensuring that mixing is thorough.

      1B. Whole Blood or Plasma: Add 0.2 ml of whole blood or plasma to 0.75 ml of TRI Reagent BD supplemented with 20 ml of 5 N acetic acid per 0.2 ml of whole blood or plasma. Close the tube and shake the solution by hand or vortex, ensuring that mixing is thorough.

      It is possible to use whole blood (blood that has been allowed to clot), serum, or plasma. Blood that has clotted would be referred to as a clot plus serum or simply as clotted blood. If you are freshly drawing the blood and adding immediately to the Tri Reagent, an anticoagulant would not be required. For serum samples, the blood is simply allowed to clot. The clot is spun down and serum is collected above the clot. If plasma is used, this indicates the blood is first drawn into either a tube containing an anticoagulant or drawn with a syringe and then transferred to a tube containing an anticoagulant. The blood is then centrifuged and the plasma is removed before adding to the Tri Reagent. We would not recommend allowing the blood to clot and then trying to add the clotted blood to the Tri Reagent.

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