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Thermo Scientific™ Maxima H Minus First Strand cDNA Synthesis Kit
Synthesize long cDNAs up to 20 kb at elevated temperatures (up to 65°C) with this complete system for highly efficient synthesis of first strand cDNA.
£107.00 - £504.00
Specifications
For Use With (Application) | Real-Time Quantitative PCR (qPCR), Reverse Transcriptase PCR (RT-PCR) |
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Product Code | Brand | Sufficient For | Price | Quantity & Availability | |||||
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Product Code | Brand | Sufficient For | Price | Quantity & Availability | |||||
10338179
|
Thermo Scientific™
K1651 |
20 reactions |
£128.00
20 reactions |
In stock, ready to ship: 7 | Please sign in to purchase this item. Need a web account? Register with us today! |
10430470
|
Thermo Scientific™
K1652 |
100 reactions |
£504.00
100 reactions |
In stock, ready to ship: 7 | Please sign in to purchase this item. Need a web account? Register with us today! |
15767526
|
Thermo Scientific™
K1651 |
20 reactions |
This item is currently unavailable or has been discontinued. View the product page for possible alternatives. |
Description
Maxima H Minus First Strand cDNA Synthesis Kit† is a complete system for highly efficient synthesis of first strand cDNA. The kit uses the Maxima H Minus Reverse Transcriptase (RT), which is an advanced enzyme derived by in vitro evolution of M-MuLV RT. The enzyme features the highest thermostability among the derivatives of M-MuLV RT and lacks RNase H activity. The Maxima H Minus First Strand cDNA Synthesis Kit allows synthesis of long cDNAs up to 20 kb at elevated temperatures (up to 65°C), superseding other systems' abilities to produce full-length cDNA. Due to increased synthesis rates the reaction can be completed in 30 minutes.
The new Maxima H Minus First Strand cDNA Synthesis Kit with dsDNase provides a dramatically simplified workflow that combines genomic DNA elimination and cDNA synthesis into one-tube procedure. The kit contains a novel double-strand specific DNase (dsDNase) engineered to remove contaminating genomic DNA from RNA preps in 2 minutes without damage to quality or quantity of RNA. Highly specific dsDNase activity towards double-stranded DNA ensures that single-stranded DNA (such as cDNA and primers) is not cleaved and dsDNase treated RNA can be directly added to reverse transcription.
Highlights
- Integrated genomic DNA removal step
- Increased reaction temperatures -the first strand of cDNA can be synthesized within the 42 to 65°C temperature range
- High yields of full-length first strand cDNA -with RNA templates up to 20 kb
- Flexible priming -oligo(dT)18, random hexamer, or gene-specific primers
Specifications
Real-Time Quantitative PCR (qPCR), Reverse Transcriptase PCR (RT-PCR) |