T4 RNA Ligase 2, truncated KQ
Product information| Code | Name | Size | Quantity | Price | |
|---|---|---|---|---|---|
M0373S |
T4 RNA Ligase 2, truncated KQ |
2.000 units ( 200000 units/ml ) | - | Unavailable in your region | |
M0373L |
T4 RNA Ligase 2, truncated KQ |
10.000 units ( 200000 units/ml ) | - | Unavailable in your region |
T4 RNA Ligase 2, truncated KQ
Not sure which ligase to choose? Refer to our DNA and RNA Ligase Properties Chart.
T4 RNA Ligase 2, truncated KQ ligates the pre-adenylated 5´ end of DNA or RNA to the 3´ end of RNA.
- Reduced lysyl adenylation activity
- Isolated from a recombinant source
- Supplied with 10X Reaction Buffer
- Requires 5' pre-adenylated RNA or DNA for ligation
- Tested for the absence of endonucleases, exonucleases, RNases and phosphatases
- Not sure which ligase to choose? Refer to our DNA and RNA Ligase Properties Chart
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Product Information
T4 RNA Ligase 2, truncated KQ (T4 Rnl2tr R55K, K227Q) specifically ligates the preadenylated 5´ end of DNA or RNA to the 3´ OH end of RNA. The enzyme does not use ATP for ligation but requires pre-adenylated linkers.
T4 Rnl2tr R55K, K227Q is a double-point mutant of T4 RNA Ligase 2, truncated (NEB #M0242). Mutation of K227 in T4 RNA Ligase 2 reduces enzyme lysyl adenylation (1). K227Q reduces the formation of undesired ligation products (concatemers and circles) by T4 Rnl2tr (2,3), by reducing the trace activity of T4 Rnl2tr in transfer of adenylyl groups from linkers to the 5´-phosphates of input RNAs (3). Mutation of R55K in T4 Rnl2tr K227Q increases the ligation activity of the enzyme to levels similar to T4 Rnl2tr (3).
The exclusion of ATP, use of pre-adenylated linkers, and the reduced enzyme lysyl adenylation activity provide the lowest possible background in ligation reactions. This enzyme has been used for optimized linker ligation for high-throughput sequencing library construction of small RNA (4).Product Source
T4 Rnl2tr R55K, K227Q is expressed as an MBP fusion from a plasmid in E. coli which encodes the first 249 amino acids of the full length T4 RNA Ligase 2 with an arginine to lysine and a lysine to glutamine mutations at positions 55 and 227, respectively.- This product is related to the following categories:
- RNA Ligation,
- RT-PCR,
- cDNA Synthesis & Reverse Transcriptases
- This product can be used in the following applications:
- RNA Cloning,
- RT-PCR & cDNA Synthesis,
- PCR
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Reagents Supplied
The following reagents are supplied with this product:
NEB # Component Name Component # Stored at (°C) Amount Concentration -
M0373S -20 T4 RNA Ligase 2, truncated KQ M0373SVIAL -20 1 x 0.01 ml 200,000 units/ml T4 RNA Ligase Reaction Buffer B0216SVIAL -20 1 x 1.5 ml 10 X 50% PEG 8000 B1004SVIAL -20 1 x 1 ml 1 X
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M0373L -20 T4 RNA Ligase 2, truncated KQ M0373LVIAL -20 1 x 0.05 ml 200,000 units/ml T4 RNA Ligase Reaction Buffer B0216SVIAL -20 1 x 1.5 ml 10 X 50% PEG 8000 B1004SVIAL -20 1 x 1 ml 1 X
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Properties & Usage
Unit Definition
200 units is defined as the amount of enzyme required to give 80% ligation of a 31-mer RNA to the pre-adenylated end of a 17-mer DNA [Universal miRNA Cloning Linker (NEB #S1315)] in a total reaction volume of 20 μl in 1 hour at 25°C.
5´-FAM- rArGrUrCrGrUrArGrCrCrUrUrUrArUrCrCrGrArGrArUrUr CrArGrCrArArUrA-3´
5´-rAppCTGTAGGCACCATCAAT–NH2-3´Reaction Conditions
1X T4 RNA Ligase Reaction Buffer
Incubate at 25°C1X T4 RNA Ligase Reaction Buffer
50 mM Tris-HCl
10 mM MgCl2
1 mM DTT
(pH 7.5 @ 25°C)Storage Buffer
10 ml Tris-HCl
100 mM NaCl
0.1 mM EDTA
1 mM DTT
50% Glycerol
pH 7.5 @ 25°CHeat Inactivation
65°C for 20 minutesMolecular Weight
Theoretical: 71378.96 daltons
Specific Activity
200,000 units/mgUnit Assay Conditions
1X T4 RNA Ligase Reaction Buffer supplemented to 10% (w/v) PEG MW 8000, 20 pmol of 5´-FAM labeled RNA, and 40 pmol preadenylated DNA linker. After incubation at 25°C for 1 hour, the ligated product is detected on a 15% denaturing polyacrylamide gel. -
Advantages and Features
Application Features
- Ligate a pre-adenylated DNA or RNA sequence tag to any RNA 3´-end
- Join a single stranded adenylated primer to small RNAs for cDNA library creation
- Join a single stranded adenylated primer to RNA for strand-specific cDNA library construction.
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Related Products
Companion Products
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Product Notes
- In our tests, this ligase can be used interchangeablywith T4 Rnl2tr (NEB #M0242). Ligationactivity is stimulated by adding PEG (See FAQ).
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References
- Yin, S., Ho, C.K. and Shuman S. (2003). J. Biol. Chem.. 278, 17601-17608.
- Hafner, M., et al. (2008). Methods. 44, 3-12.
- Viollet, S., et al. (2011). BMC Biotechnol. 11, 72.
- Zhuang, F., et al. (2012). Nucleic Acids Res.. 40(7), e54.
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Protocols, Manuals & Usage
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Tools & Resources
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FAQs & Troubleshooting
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FAQs
- Is T4 RNA Ligase 2, truncated KQ different than T4 RNA Ligase 2, truncated K227Q?
- Are there differences in ligation efficiency for T4 RNA Ligase 2, truncated KQ, T4 RNA Ligase 2, truncated 227Q, and T4 RNA Ligase 2, truncated KQ?
- What can T4 RNA Ligase 2, truncated KQ ligate?
- Does PEG stimulate ligation efficiency?
- How can I increase ligation efficiency?
- Can T4 RNA Ligase 2, truncated KQ be used in other NEBuffers?
- The molecular weight of T4 RNA Ligase 2, truncated KQ is 71.6 kDa. Is it a fusion?
- Is PEG 8000 available for purchase?
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Citations & Technical Literature
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Citations
Product Citation Tool
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Quality, Safety & Legal
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Quality Control Assays
Quality Control tests are performed on each new lot of NEB product to meet the specifications designated for it. Specifications and individual lot data from the tests that are performed for this particular product can be found and downloaded on the Product Specification Sheet, Certificate of Analysis, data card or product manual. Further information regarding NEB product quality can be found here. -
Specifications & Change Notifications
The Specification sheet is a document that includes the storage temperature, shelf life and the specifications designated for the product. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version] -
Certificate of Analysis
The Certificate of Analysis (COA) is a signed document that includes the storage temperature, expiration date and quality controls for an individual lot. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]_[Lot Number]- M0373S_L_v1_0031804
- M0373S_L_v1_0031710
- M0373L_v1_10008697
- M0373S_v1_10008698
- M0373L_v2_10028372
- M0373S_v2_10028369
- M0373L_v2_10041612
- M0373S_v2_10041614
- M0373L_v2_10052059
- M0373L_v2_10057255
- M0373S_v2_10052062
- M0373L_v2_10062650
- M0373S_v2_10065560
- M0373L_v2_10070020
- M0373L_v2_10084293
- M0373S_v2_10084296
- M0373L_v2_10105435
- M0373S_v2_10112133
- M0373L_v2_10122069
- M0373L_v2_10127451
- M0373S_v2_10127450
- M0373L_v2_10140375
- M0373S_v2_10146863
- M0373L_v2_10166706
- M0373S_v2_10166708
- M0373L_v2_10183116
- M0373S_v2_10196881
- M0373L_v2_10208820
- M0373S_v2_10219415
- M0373L_v2_10242298
- M0373S_v2_10242317
- M0373L_v2_10269184
- M0373S_v2_10274794
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Safety Data Sheets
The following is a list of Safety Data Sheet (SDS) that apply to this product to help you use it safely. -
Legal and Disclaimers
Products and content are covered by one or more patents, trademarks and/or copyrights owned or controlled by New England Biolabs, Inc (NEB). The use of trademark symbols does not necessarily indicate that the name is trademarked in the country where it is being read; it indicates where the content was originally developed. The use of this product may require the buyer to obtain additional third-party intellectual property rights for certain applications. For more information, please email busdev@neb.com.
This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.
New England Biolabs (NEB) is committed to practicing ethical science – we believe it is our job as researchers to ask the important questions that when answered will help preserve our quality of life and the world that we live in. However, this research should always be done in safe and ethical manner. Learn more.
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