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Aav expression vector

Manufactured by Takara Bio

The AAV expression vector is a laboratory tool designed to facilitate the production and study of adeno-associated viruses (AAVs). AAVs are small, non-pathogenic viruses that can be used as gene delivery vehicles. The AAV expression vector provides the necessary genetic components for the efficient generation and expression of recombinant AAV particles in a laboratory setting.

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2 protocols using aav expression vector

1

Synthesis, Cloning, and Verification of AAV Constructs

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DNA fragments were synthesized as IDT gBlocks Gene Fragments and/or oligonucleotides and amplified by PCR using Q5 Hot Start (New England Biolabs), and cloned into an AAV expression vector (Addgene plasmid # 20299) using In-Fusion HD (Takara Bio) or NEBuilder HiFi (New England Biolabs), replacing the FLEX-mCherry construct originally in the vector. Descriptions of all the constructs tested are listed in Supplementary Table 1. The constructs used for multiplexed EM labeling in the study are bolded in Supplementary Table 1. All constructs were verified using Sanger sequencing and maintained in NEB Stable E. coli (New England Biolabs). Plasmids generated in this study (Table 1) were deposited to Addgene.
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2

Synthesis, Cloning, and Verification of AAV Constructs

Check if the same lab product or an alternative is used in the 5 most similar protocols
DNA fragments were synthesized as IDT gBlocks Gene Fragments and/or oligonucleotides and amplified by PCR using Q5 Hot Start (New England Biolabs), and cloned into an AAV expression vector (Addgene plasmid # 20299) using In-Fusion HD (Takara Bio) or NEBuilder HiFi (New England Biolabs), replacing the FLEX-mCherry construct originally in the vector. Descriptions of all the constructs tested are listed in Supplementary Table 1. The constructs used for multiplexed EM labeling in the study are bolded in Supplementary Table 1. All constructs were verified using Sanger sequencing and maintained in NEB Stable E. coli (New England Biolabs). Plasmids generated in this study (Table 1) were deposited to Addgene.
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