One-Stop Solution For CceAAV Production Service

A conventional recombinant single-stranded AAV (ssAAV) and self-complementary AAV (scAAV) package the genome with wild-type ITRs or mutated ITRs flanking an expression cassette encoding a gene of interest. Upon uncoating in target cells, scAAV can rapidly form an intra-molecular double-stranded DNA, facilitating high-level transgene expression.

In our proprietary cceAAV (covalently closed end double stranded AAV) technology, we used a 56-bp recognition sequence of protelomerase (Tel N) to covalently join the top and bottom strands, allowing the vector to be generated with just a single ITR. To produce cceAAV vectors, the vector plasmid is initially digested with Tel N, purified, and then subjected to a standard triple-plasmid transfection protocol followed by traditional AAV vector purification procedures.

CceAAV allows for an increased packaging capacity compared to scAAV vectors due to a higher formation rate of hairpin loops in vitro and fewer nucleotides than the mutated ITR. Analysis on Alkaline Agarose gel indicates that cceAAV viruses have a lower fraction of unexpected partial genomes compared to scAAV, suggesting potential enhancement in potency and reduced safety concerns.

We provide one-stop solution for cceAAV Production Service including plasmid preparation, high-quality at affordably priced Tel N enzyme and cceAAV production service to meet the customer convenience of cceAAV quick testing.

One-Stop Solution For CceAAV Production Service

categoryIDSample nameSpecificationDescriptionAdd to cart
EnzymeTel N enzyme500U/1000U/2500U/5000UCuts dsDNA at a TelN recognition sequence (56 bp) and leaves covalently closed ends at the site of cleavage
Plasmid preparationpCceAAV-CB-EGFP5mg/10mgpAAV with one Tel N and CB promoter and EGFP expression gene (without Tel N enzyme treatment)
Plasmid preparationpScAAV-CB-EGFP5mg/10mgpAAV with one trs deleted ITR and CB promoter and EGFP expression gene
Plasmid preparationpCceAAV-CB-EGFP (Tel N)5mg/10mgpAAV with one Tel N and CB promoter and EGFP expression gene treated with Tel N and purified, could be used for AAV production
Plasmid preparationpCceAAV-CB-Gluc5mg/10mgpAAV with one Tel N and CB promoter and Gluc expression gene (without Tel N enzyme treatment)
Plasmid preparationpScAAV-CB-Gluc5mg/10mgpAAV with one trs deleted ITR and CB promoter and Gluc expression gene
Plasmid preparationpCceAAV-CB-Gluc (Tel N)5mg/10mgpAAV with one Tel N and CB promoter and Gluc expression gene treated with Tel N and purified, could be used for AAV production
Plasmid preparationpCceAAV-TTR-hFIX5mg/10mgpAAV with one Tel N and murine promoter TTR and R338LhFIXco expression gene (without Tel N enzyme treatment)
Plasmid preparationpScAAV-TTR-hFLX5mg/10mgpAAV with one trs deleted ITR and murine promoter TTR and R338LhFIXco expression gene
Plasmid preparationpCce-TTR-hFIX (Tel N)5mg/10mgpAAV with one Tel N and murine promoter TTR and R338LhFIXco expression gene treated with Tel N and purified, could be used for AAV production
AAV productionscAAV-CB-EGFPscAAV package with CB promoter and GFP expression gene as required serotype
AAV productioncceAAV- CB-EGFPcceAAV package with CB promoter and GFP expression gene as required serotype
AAV productionscAAV- CB-GluccceAAV package with CB promoter and GFP expression gene as required serotype
AAV productioncceAAV- CB-GluccceAAV package with CB promoter and Gluc expression gene as required serotype
AAV productionScAAV-TTR-hFLXcceAAV package with murine promoter TTR and R338LhFIXco expression gene as required serotype
AAV productioncceAAV-TTR-hFIXcceAAV package with murine promoter TTR and R338LhFIXco expression gene as required serotype
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