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View additional product information for pLenti6.3/V5-DEST™ Gateway™ Vector Kit - FAQs (V53306)
9 product FAQs found
In the single-step protocol for the BP/LR Clonase reaction, we would not recommend substituting the BP Clonase II/LR Clonase II enzymes with BP Clonase /LR Clonase enzymes as this would result in very low recombination efficiency.
Yes, we have come up with a single-step protocol for BP/LR Clonase reaction (http://www.thermofisher.com/us/en/home/life-science/cloning/gateway-cloning.html#1), where DNA fragments can be cloned into Destination vectors in a single step reaction, allowing you to save time and money.
We would recommend performing a BP reaction with a Donor vector in order to obtain an entry clone. This entry clone can then be used in an LR reaction with the Destination vector to obtain the new expression clone.
We do not offer the 5X LR Clonase buffer and 5X BP Clonase buffer as standalone products. They are available as part of the enzyme kits.
We do not offer any Gateway vectors for expression in plants.
Our vectors have not been completely sequenced. Your sequence data may differ when compared to what is provided. Known mutations that do not affect the function of the vector are annotated in public databases.
No, our vectors are not routinely sequenced. Quality control and release criteria utilize other methods.
Sequences provided for our vectors have been compiled from information in sequence databases, published sequences, and other sources.
Unfortunately, we do not offer the pLenti6.3/V5-DEST Gateway vector as a stand-alone product. The pLenti6.3/V5-DEST Gateway vector is offered as a component of the pLenti6.3/V5-DEST Gateway Vector Kit (Cat. No. V53306) or as part of the ViraPower HiPerform Lentiviral Gateway Expression Kit (Cat. No. K5330-00).
Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.