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shRNA重组AAV病毒定制生产
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shRNA AAV Production Service:
Adeno-associated virus (AAV) is a small virus (20 nm in diameters)
replication-defective, nonenveloped virus, which infects humans and some other
primate species. AAV is not currently known to cause disease and consequently
the virus causes a very mild immune response. AAV can infect both dividing and
non-dividing cells and may incorporate its genome into that of the host cell.
With our proprietary genetically engineered AAV·HT™ packaging cell, we are
offering shRNA rAAV (conventional single stranded rAAV or double-stranded rAAV
also called self-complementary rAAV*) production services for efficient silencing in vitro
and in vivo.
If commercial shRNAs or siRNAs of your target gene are not available or
non-functional, or your project requires special design for further development,
we offer special shRNA design without additional charge!
Advantages:
- One-stop service: from shRNA design to packaging.
- High infection efficiency.
- Quick turnaround time: 2 to 3 weeks.
- Cost-effective.
- Special design request acceptable, FREE!
Wide choice of rAAV cis vectors:
Requirements: GenBank access #,
sequence of gene of interest or shRNA is needed.
Deliverables: Total >1.0 ml at >1013 VG/ml** shRNA rAAV
for large scale production.
With our proprietary genetically engineered AAV·HT™ packaging cell
and a modified rAAV cis plasmid, the shRNA rAAV yield is easy to reach super high level--------total
1E+15 VG.
For super high level rAAV production up to 1E+15 VG , please
contact us to request a quote.
* Some terms may apply for custom double-stranded or self-complementary rAAV production
service.
** Final viral yield may depend on the transgene
in the virus.
For rAAV serotype 2, we guarantee final
deliverable of >2.0 ml at >1E+12 VG/ml.
显示1至6 (共6件产品)
| 型号 |
产品名称- |
价格 |
| SL100810 |
Features: - Excellent gene delivery efficiency in most cell types including dividing and non-dividing or primary cells. - Multiple serotypes (AAV1, AAV2, AAV5, AAV6, AAV8, AAV9). - Integration into chromosome 19 of host genome. - Induce efficient gene silencing. Wide Choice of AAV cis Vectors: Service Description: 1. Synthesize and clone shRNA into AAV cis vectors. 2. Large scale transfection of AAV·HT™ 293 cells into 2xcell stack. 3. Harvest rAAV... |
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| SL100871 |
Features: - Excellent gene delivery efficiency in most cell types including dividing and non-dividing or primary cells. - Multiple serotypes (AAV1, AAV2, AAV5, AAV6, AAV8, AAV9). - Integration into chromosome 19 of host genome. - Induce efficient gene silencing. Wide Choice of AAV cis Vectors: Service Description: 1. Synthesize and clone shRNA into AAV cis vectors. 2. Medium scale transfection of AAV·HT™ 293 cell into 1xcell stack. 3. Harvest rAAV... |
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| SL100874 |
Features: - Excellent gene delivery efficiency in most cell types including dividing and non-dividing or primary cells. - Multiple serotypes (AAV1, AAV2, AAV5, AAV6, AAV8, AAV9). - Integration into chromosome 19 of host genome. - Induce efficient gene silencing. Wide Choice of AAV cis Vectors: Service Description: 1. Synthesize and clone shRNA into AAV cis vectors. 2. Pilot scale transfection of AAV·HT™ 293 cell into 10x150 mm plates. 3. Harvest rAAV... |
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| SL100872 |
Features: - Excellent gene delivery efficiency in most cell types including dividing and non-dividing or primary cells. - Multiple serotypes (AAV1, AAV2, AAV5, AAV6, AAV8, AAV9). - Integration into chromosome 19 of host genome. - Induce efficient gene silencing. - Wide choice of AAV cis vectors (promoterless, CMV, CAG (also known as CBA), U6, H1, UBC, Synapsin promoters with or without reporter genes like GFP, mRFP, Luc, LacZ, etc). Service Description: -... |
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| SL100873 |
Features: - Excellent gene delivery efficiency in most cell types including dividing and non-dividing or primary cells. - Multiple serotypes (AAV1, AAV2, AAV5, AAV6, AAV8, AAV9). - Integration into chromosome 19 of host genome. - Induce efficient gene silencing. - Wide choice of AAV cis vectors (promoterless, CMV, CAG (also known as CBA), U6, H1, UBC, Synapsin promoters with or without reporter genes like GFP, mRFP, Luc, LacZ, etc). Service Description: -... |
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| SL100875 |
Cell-based shRNA Validation Service: - Cloning cDNA of your targeted gene into a validation plasmid - Design and synthesize ~6 shRNA oligoes followed by cloning them to a rAAV cis vector. - Transient co-transfection cDNA/shRNA plasmids. - Quantification of target gene silencing via qRT-PCR Available shRNA Validation Platforms: - Constitutive shRNA knockdown - Inducible shRNA knockdown Guaranteed Knockdown: We guarantee the knockdown of >80% at mRNA level in... |
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显示1至6 (共6件产品)
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