Data is not available to indicate whether DNA contamination could affect sequencing. However, including DNase treatment is recommended to minimize genomic DNA in the sequencing reads.
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| Voi/SKU | Disponibilità | Prezzo |
|---|---|---|
1 kit | Per conoscere la disponibilità, visualizza il carrello | CHF 1700.00 |
Informazioni su questo articolo
usage
sufficient for 250 purifications
Quality Segment
greener alternative product characteristics
Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.
sustainability
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technique(s)
RNA purification: suitable
test parameters
: ~30 min kit run time, sample volume: 100 mg
greener alternative category
storage temp.
15-25°C
General description
Dopo la polverizzazione che riduce il tessuto a una polvere sottile in azoto liquido, le cellule vengono lisate e i detriti cellulari sono separati fisicamente e chimicamente dall′RNA endogeno. L′RNA viene quindi legato a un substrato di silice supportato in colonna e i contaminanti rimasti vengono rimossi attraverso diverse fasi di lavaggio.
L′RNA totale viene eluito dalla colonna e usato nelle applicazioni tipiche, come il Northern blot e la PCR RT e qRT.
Application
- estrarre l'RNA da materiale macinato in azoto liquido
- isolare l'RNA totale da piantine mutanti e wt (wild type)
- per estrarre l'RNA totale da campioni di foglie
- per estrarre l'RNA da tutti i tipi di tessuti vegetali
Features and Benefits
- Resa massima di 60 μg di RNA puro concentrato per preparazione
- Un protocollo efficiente consente di purificare l′RNA in non più di 30 minuti
- Progettato in particolar modo per la ricerca su tessuti vegetali difficili
Legal Information
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Questo articolo | |||
|---|---|---|---|
| description sufficient for 250 purifications | description sufficient for 50 purifications | description sufficient for 10 purifications | description sufficient for 70 purifications |
| technique(s) RNA purification: suitable | technique(s) RNA purification: suitable | technique(s) RNA purification: suitable | technique(s) DNA purification: suitable |
| usage sufficient for 250 purifications | usage sufficient for 50 purifications | usage sufficient for 10 purifications | usage sufficient for 70 purifications |
| greener alternative category | greener alternative category | greener alternative category , Aligned | greener alternative category , Aligned |
| storage temp. 15-25°C | storage temp. 15-25°C | storage temp. 15-25°C | storage temp. 15-25°C |
| greener alternative product characteristics Designing Safer Chemicals | greener alternative product characteristics Designing Safer Chemicals | greener alternative product characteristics Designing Safer Chemicals | greener alternative product characteristics Inherently Safer Chemistry for Accident Prevention |
| sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product | sustainability Greener Alternative Product |
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Solo come componenti del kit
- Binding Solution
- Lysis Solution
- Wash Solution 1
I componenti del kit sono disponibili anche separatamente
- 2-Mercaptoethanol, Molecular Biology, suitable for electrophoresis, suitable for cell culture, BioReagent, 99% (GC/titration) 2
Parola di avvertenza
Danger
Codici di pericolo
Avvertenze di sicurezza
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral
Organi bersaglio
Liver,Heart
Classe di stoccaggio
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
Che succede?
WGK 3
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I’m using your plant RNA extraction kit for RNA-seq. If I skip the DNase treatment, could DNA contamination affect the sequencing library, or is it mandatory to include this step? Thank you.
1 answer-
Helpful?
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does it sufficient for small RNA and/or non-coding RNA extraction?
1 answer-
Yes, this kit is sufficient for small RNA. However, It is worth noting that small RNA molecules, such as microRNA, siRNA, tRNA, 5S rRNA, are not efficiently recovered using the standard procedure. If desired, these small RNA molecules can be recovered by increasing the amount of binding solution, as described in Protocol A under Procedure Step 4.
For more information, please see the protocol associated with this product:
https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/323/177/strn250bul.pdfHelpful?
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