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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| Rozmiar/SKU | Dostępność | Cena netto |
|---|---|---|
1 kit | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 8410,00 zł |
Informacje o tej pozycji
8410,00 zł
usage
sufficient for 250 purifications
Quality Segment
sustainability
Sustainability features
technique(s)
RNA purification: suitable
test parameters
: ~30 min kit run time, sample volume: 100 mg
storage temp.
15-25°C
General description
After grinding tissue to a fine powder in liquid nitrogen, cells are lysed and cellular debris is physically and chemically separated from endogenous RNA. RNA is then bound to a column supported silica substrate and several wash steps remove remaining contaminants.
Total RNA is eluted from the column and used in typical applications, such as Northern Blots, and RT- and qRT-PCR.
Application
- to extract RNA from the material ground in liquid nitrogen
- to isolate total RNA from mutant and wt (wild type) plantlets
- to extract total RNA from leaf samples
- to extract RNA from all plant tissues
Features and Benefits
- Yields up to 60 μg of pure concentrated RNA per prep
- Efficient protocol allows for RNA purification in 30 min or less
- Specially designed for research with difficult plant tissues
Legal Information
1 of 1
Ta pozycja | |||
|---|---|---|---|
| description sufficient for 250 purifications | description sufficient for 50 purifications | description sufficient for 10 purifications | description sufficient for 100 extractions, sufficient for 100 amplifications |
| usage sufficient for 250 purifications | usage sufficient for 50 purifications | usage sufficient for 10 purifications | usage sufficient for 100 extractions, sufficient for 100 reactions, sufficient for 100 amplifications |
| technique(s) RNA purification: suitable | technique(s) RNA purification: suitable | technique(s) RNA purification: suitable | technique(s) PCR: suitable, whole genome amplification: suitable |
| test parameters : ~30 min kit run time, sample volume: 100 mg | test parameters sample volume: 100 mg, : ~30 min kit run time | test parameters sample volume: 100 mg, : ~30 min kit run time | test parameters - |
| storage temp. 15-25°C | storage temp. 15-25°C | storage temp. 15-25°C | storage temp. - |
| greener alternative category | greener alternative category | greener alternative category | greener alternative category - |
| sustainability Sustainability features | sustainability Sustainability features | sustainability Sustainability features | sustainability - |
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Słowo ostrzegawcze
Danger
Kody zagrożeń
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
Narządy docelowe
Liver,Heart
Klasa składowania
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
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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