Determine the necessary mass, volume, or concentration for preparing a solution.
for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Avoid repeated freezing and thawing Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
T4 DNA Ligase is isolated and purified from Escherichia coli expressing the T4 DNA Ligase gene after induction and expression. It catalyzes the binding reaction of adjacent DNA strands with 5 'phosphate groups and 3' hydroxyl groups via phosphodiester bonds. This enzyme can catalyze the connection of flat or sticky end DNA, repairing single stranded incisions in double stranded DNA, RNA, and DNA/RNA hybridization, but has no activity for single stranded nucleotides.
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Activity definition:
1U refers to the amount of enzyme required to convert 1nmol [32PPi] into Norit absorbable form within 20 minutes at 37 ° C in the ATP-PPi exchange reaction, equivalent to approximately 200 viscous terminal junction units.
Application scope:
Mainly used for adapter connection during the construction process of NGS Chinese library.
Usage:
It is recommended to use Kangwei Adaptor for connection, or choose to use Adaptors from NEB or Illumina companies. For specific connection methods, please refer to the product manuals of each company. The following are the steps to connect using Kangwei Adaptor:
1. Directly add the following reagents to the reaction solution that has completed DNA end repair:
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At this point, the total volume of solution in the tube is 100 μ L.
Note: If the initial sample size is less than 100 ng, please dilute the adapter 10 times with deionized water to 1.5 μ Use after M.
2. Use a gun to blow and aspirate the above reagents, mix well, and centrifuge briefly to collect the solution to the bottom of the tube.
Take a warm bath at
3.23 ℃ for 20 minutes.
Attention: If using a PCR instrument for this operation, please close the heat cap.
4. Continue with subsequent steps, such as selective recovery of DNA fragments or purification of DNA fragments.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →