Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
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| Größe/SKU | Verfügbarkeit | Preis |
|---|---|---|
10 reactions | Warenkorb auf Verfügbarkeit prüfen | € 192,00 |
50 reactions | Warenkorb auf Verfügbarkeit prüfen | € 641,00 |
500 reactions | Warenkorb auf Verfügbarkeit prüfen | € 5.100,00 |
Über diesen Artikel
€ 192,00
Quality Segment
technique(s)
whole genome amplification: suitable
dilution
(WGA)
input
purified DNA
shipped in
wet ice
storage temp.
−20°C
General description
Application
Features and Benefits
- Höhere Ausbeute aus einer minimalen Matrize: Amplifikation von Nanogramm-Mengen genomischer DNA zu Mikrogramm-Ausbeuten (etwa 10 μg) in weniger als etwa drei Stunden
- Nanogramm-Mengen von Proben können bei -20 °C für die zukünftige Verwendung konserviert werden
- Vielfältige DNA-Quellen können eingesetzt werden: Vollblut, Wangenabstriche, Blutkarten, Pflanzen, Bodenproben und Formalin-fixiertes Paraffin eingebettetes (FFPE) Gewebe
- Gesamtgenom-Amplifikation(GGA)-DNA-Polymerase steigert die Genauigkeit der Amplifikation
- Gesamtgenom-Repräsentation ohne nachweisbare allelische Verzerrung
- Mit den meisten Downstream-Anwendungen wie TaqMan®-Assays, Einzelnukleotid-Polymorphismus(SNP)-Analyse, CGH-Microarray-Analyse (vergleichende genomische Hybridisierung) kompatibel
Other Notes
Legal Information
1 of 1
Dieser Artikel | |||
|---|---|---|---|
| description Optimized kit with enzyme for amplifying a variety of DNA including FFPE tissue | description Kit for whole genome amplification from a variety of DNA sources including FFPE tissue | description Amplify genome of a single cell | description Reamplification of WGA product with minimal bias |
| technique(s) whole genome amplification: suitable | technique(s) whole genome amplification: suitable | technique(s) whole genome amplification: suitable | technique(s) whole genome amplification: suitable |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. −20°C |
| dilution (WGA) | dilution (WGA) | dilution (WGA) | dilution (WGA) |
| input purified DNA | input purified DNA | input purified DNA | input purified DNA |
| shipped in wet ice | shipped in wet ice | shipped in wet ice | shipped in wet ice |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
Signalwort
Danger
Gefahrencodes
Sicherheitshinweise
Hazard Classifications
Resp. Sens. 1
Lagerklasse
12 - Non Combustible Liquids
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
WGK
WGK 3
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What is the Department of Transportation shipping information for this product?
1 answer-
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Is the WGA2 GenomePlex® Amplification Kit polymerase compatible with TA cloning?
1 answer-
WGA polymerase is compatible with TA cloning with the following alteration to the PCR step: Be sure to include a 7 to 30 minute extension at 72°C after the last cycle to ensure that all PCR products are full length and 3´ adenylated.
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If starting with fragmented DNA, what is the smallest size fragment which can be successfully amplified with Product WGA2, GenomePlex® Amplification Kit, and do I still need to do the fragmentation step?
1 answer-
The kit works best for fragments 400 bp and larger. When starting with fragmented DNA, we recommend: (1) skipping the fragmentation heat step, although the buffer should be added, and (2) increasing the PCR cycles from 14 to 20.
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Can I use Product WGA2, GenomePlex® Amplification Kit, to amplify DNA from a single cell?
1 answer-
Using this kit to amplify DNA from a single cell is not recommended. We recommend using the GenomePlex Single Cell WGA Kit (WGA4) for such application. WGA4 was developed for use with single cells and includes an optimized cell lysis protocol which has been incorporated into the fragmentation step.
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What is the major difference between WGA1 and WGA2 kits?
1 answer-
Functionally, WGA1 and WGA2 kits are identical. The only difference between the two kits is that WGA2 is supplied with the WGA polymerase.
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Can I amplify single stranded DNA with WGA2, GenomePlex® Amplification Kit?
1 answer-
When starting with single stranded starting materials, we recommend (1) skipping the fragmentation heat step, although the buffer should be added and (2) increasing the PCR cycles from 14 to 20. Note that if the ssDNA is actually cDNA from polyadenylated RNA, the kit will likely not give good representation of the input material, as the poly(T) ends constitute a large, non-random fraction.
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