DNA Fragmentation & Blunting Enzyme Mix
Fast and simple fragmentation
Fragment size easily controlled by incubation time
Ideal for NGS library preparation
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General Description
SmartRTTM Reverse Transcriptase is an engineered MMLV RT that improves the enzyme’s thermostability, reduces RNase H activity and its cDNA synthesis ability. The enzyme also has a terminal transferase activity, where it adds a few extra nucleotides to the end of the synthesized cDNA. With a 3’ modified oligo dT primer and a 5’ SMART universal oligo containing a terminal complementation to nucleic acids at the 3’ end of the first-strand cDNA, the SmartRTTM reverse transcriptase will produce RACE ready full-length cDNA.
Features
MCLAB's reverse transcriptase is one of transcriptases that has the highest thermostability with terminal transferase activity.
Source
E. coli
Applications
Reverse transcription and RACE ready full length cDNA synthesis
Supplied with
5 x first strand cDNA synthesis buffer
Recommended Storage Condition
-20 °C
Unit Definition
One unit is defined as the amount of enzyme that will incorporate 1 nmol of dTTP into acid-insoluble material in 10 minutes at 37°C using poly(A):oligo(dT) as template:primer.
Shipping Condition
dry ice
User protocol
For RACE ready first-strand cDNA Synthesis
Combine the following in separate 0.2-ml PCR tubes (20 µl reaction):
1–9 µl RNA sample
1 µl 5’ SMART universal Primer
1 µl oligo dT Primer
1 µl dNTP
Add sterile H2O to a final volume of 12 µl for each reaction.
Incubate the tubes at 65°C for 5 min
Cool the tubes on ice for 3 min
Add the following to each reaction tube:
4 µl 5X First-Strand Buffer
1 µl DTT (20 mM)
2 µl dNTP Mix (10 mM)
2 µl SmartRT reverse transcriptase
Incubate the tubes:
50°C for 1.5 hr
85°C for 5 min
For regular first-strand cDNA Synthesis
Combine the following in separate 0.2-ml PCR tubes (20 µl reaction):
1–10 µl RNA sample
1 µl oligo dT Primer or Random primer
1 µl dNTP
Add sterile H2O to a final volume of 12 µl for each reaction.
Incubate the tubes at 65°C for 5 min
Cool the tubes on ice for 3 min
Add the following to each reaction tube:
4 µl 5X First-Strand Buffer
1 µl DTT (20 mM)
2 µl dNTP Mix (10 mM)
2 µl SmartRT reverse transcriptase
Incubate the tubes:
50°C for 45 min
85°C for 5 min
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Fast and simple fragmentation
Fragment size easily controlled by incubation time
Ideal for NGS library preparation
High efficiency
Low GC bias
Input DNA: 500 pg to 1 µg
Fast and easy ligation
High efficiency
Optimized formulation
Fast and simple fragmentation
Fragment size easily controlled by incubation time
Ideal for NGS library preparation
Fast and simple fragmentation
Fragment size easily controlled by incubation time
Ideal for NGS library preparation
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