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Overview
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pSpark® TA is efficient, stable and easy-to-use DNA cloning vector based on an optimized TA technology for cloning single 3 ́-adenine overhanging DNA. The vectors are prepared by digestion of pSpark® TA at EcoRV site and the subsequent addition of a single thymidine at each 3 ́- end to allow cloning Taq DNA Polymerase amplified DNA fragments. Its exclusive procedure offers greater efficiency and less background of blue colonies than the others TA vectors. Quote request
Includes for 20 rxn:
– 20 µL pSpark® TA (50 ng/µL)
– 20 µL T4 DNA Ligase (5U/Weiss)
– 200 µL T4 DNA Ligase Buffer (5x)
– 5 µL Insert Control 600 bp (30 ng/µL)Please contact us at for specific academic pricing.
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- Properties
- Applications
- Reference
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Overview