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Asana BioSciences, LLC Protocol ASN002AD202 Protocol version 6.0: 01 October 2019Page 2 of 84TABLE OF CONTENTS TABLE OF CONTENTS ............................................................................................................2
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01
Design primers to amplify the DNA fragments to be inserted into the vector.
02
Optimize PCR conditions to ensure specific amplification of the DNA fragments.
03
Purify the amplified DNA fragments using a PCR cleanup kit.
04
Set up the In-Fusion reaction mix according to the manufacturer's instructions.
05
Add the purified DNA fragments and vector into the reaction mix.
06
Incubate the reaction mix at the specified temperature for the recommended time.
07
Transform the In-Fusion reaction mix into competent cells.
08
Select transformed cells using appropriate antibiotics.
09
Confirm successful insertion of multiple DNA fragments through sequencing or restriction digestion.

Who needs in-fusion snap assembly multiple-insert?

01
Researchers working on gene cloning and molecular biology experiments that require the simultaneous insertion of multiple DNA fragments into a vector.
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In-fusion snap assembly multiple-insert is a method used in molecular biology for efficient and seamless cloning of multiple fragments into a single vector.
Researchers or scientists working in the field of molecular biology are required to utilize in-fusion snap assembly multiple-insert technique for specific cloning purposes.
In-fusion snap assembly multiple-insert is filled out by designing primers for the fragments to be cloned, followed by PCR amplification and assembly using the in-fusion cloning kit.
The purpose of in-fusion snap assembly multiple-insert is to enable the cloning of multiple DNA fragments into a single vector in a seamless and efficient manner.
Information such as primer sequences, fragment sizes, vector details, and cloning strategy must be reported on in-fusion snap assembly multiple-insert.
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