R4533
RNAzol® RT
For processing total and small RNA from human, animal, plant, bacterial,and viral samples
Synonyme(s) :
single step RNA isolation, single step RNA purification, total RNA isolation, total RNA purification
About This Item
Niveau de qualité
Utilisation
mL sufficient for 107 cells
mL sufficient for 100 mg tissue (or)
Catégories apparentées
Description générale
This product, a mixture of guanidine thiocyanate and phenol in a monophase solution, effectively dissolves DNA, RNA, and protein on homogenization or lysis of tissue sample. Addition of water to the mixture allows for the precipitation of DNA, proteins, polysaccharides and other molecules, which can then be removed by centrifugation. RNA can then be isolated by alcohol precipitation, washing and solubilization. Chloroform-induced phase separation is not necessary. One mL of RNAzol® RT is sufficient to isolate RNA from up to 100 mg of tissue or 10e7 cells.
This is one of the most effective methods for isolating total and small RNA and can be completed at room temperature in less than 1 hour starting with fresh tissue or cells. The procedure is very effective for isolating RNA molecules of all types: large nuclear RNA, rRNA, mRNA, small RNA and micro RNA. The resulting RNA is intact with little or no contaminating DNA and protein.
Application
Caractéristiques et avantages
- Isolates micro RNA and total RNA isolation of pure and undegraded RNA from biological samples
- High yields and increased quality of isolated RNA
- Completed at room temperature in less than an hour starting with fresh tissue or cells
Informations légales
Produit(s) apparenté(s)
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B - STOT RE 2
Code de la classe de stockage
8A - Combustible, corrosive hazardous materials
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
230.0 °F
Point d'éclair (°C)
110 °C
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Articles
The availability of simple methods for purification of DNA and RNA has greatly facilitated the analysis and characterization of the genome and gene expression. There is a demand to isolate DNA and RNA rapidly and conveniently from a variety of cellular sources, including cells and tissues from mammalian, plant and bacterial cultures.
Protocoles
Method for purification, reverse transcription and quantitative PCR for MicroRNAs using Mysticq reagents
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