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Adenovirus (Ad) packaging services
Adenovirus (Ad) packaging services
Adenoviral vector has high transduction efficiency and high levels of short-term gene expression, and is widely used in cell and gene therapy applications. BrainVTA offers custom Adenovirus Service where include gene synthesize, clone and viral package for you. No matter what you needed, our team of scientists will work with you to provide the custom Adenoviral packaging service that best meets your needs.
Adenovirus (Ad) packaging services
Adenoviral vector has high transduction efficiency and high levels of short-term gene expression, and is widely used in cell and gene therapy applications. BrainVTA offers custom Adenovirus Service where include gene synthesize, clone and viral package for you. No matter what you needed, our team of scientists will work with you to provide the custom Adenoviral packaging service that best meets your needs.
Custom Adenovirus Vector Design
We also provide Cloning Services to allow you to fully customize your order at a reasonable cost and with a quick turn around time, include over-express any genes (wildtype, mutant or synthetic) or to silence/knock-down/knock-out/knock-in any genes. Please contact us with your project details and our team will get in touch as soon as possible with an estimated price and projected turnaround time. You can also visit our Molecular Cloning page for more information. If you already have the ORF in plasmids, you just need to send the min- plasmid to us, then we will clone in Adenovirus vector and package it.
Recombinant Lentivirus packaging services
BrainVTA provides the complete AdV vectors and AdV Expression Systems that can be used to express human/mouse/rat ORFs, lncRNAs, circRNAs, shRNAs, CRISPR/gRNA in vitro and in vivo studies. Our optimized adenoviral vector production and strict quality control systems provide customers a high titer of functional recombinant adenoviral vectors. Viral titers are determined by TCID50 method, which is the most accurate way to measure the titer of adenovirus.
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BrainVTA offers tailor-made AAVs for the customers and presents a wide variety of options to choose from. All customized services undergo stringent control to guarantee the quality of the viral partic
Adenoviral vector has high transduction efficiency and high levels of short-term gene expression, and is widely used in cell and gene therapy applications. BrainVTA offers custom Adenovirus Service wh
BrainVTA provide lentivirus services ranging from small-scale lentivirus packaging to large scale lentivirus packaging for in vitro and in vivo studies. We have developed a series of proprietary techn
Lentivirus (LVs) are single stranded RNA (sRNA) viruses, which are a subgroup of the retrovirus family. They can integrate into the host genome in both dividing and non-dividing cells, with a wide ran
Lentivirus (LVs) are single stranded RNA (sRNA) viruses, which are a subgroup of the retrovirus family. They can integrate into the host genome in both dividing and non-dividing cells, with a wide ran
A monoclonal cell line is essentially generated from an original polyclonal population, but it is required to separate from the polyclonal pool in order to create a pure, monoclonal cell line that is
Intrathecal injection is a technique used to deliver drugs, viral vectors, or tracers directly into the cerebrospinal fluid (CSF) via the spinal canal.
In contrast to transient expression, stable expression allows long term, as well as defined and reproducible, expression of the gene of interest
Temporal vein injection is a technique used to deliver substances systemically via the superficial temporal vein, commonly in neonatal rodents.
Isolation, dissociation, and culture of primary neurons from brain tissue, followed by incubation in Neurobasal medium for maturation and dendrite formation.
BrainVTA offers comprehensive cloning services to create custom DNA constructs with 100% accuracy, providing fast delivery, various vector and marker options, and cost-effective solutions to save rese
Renal pelvis injection is a technique for delivering substances directly into the kidney’s collecting system.
Subretinal injection is a precise method used to deliver substances such as viral vectors, stem cells, or drugs into the subretinal space
Non-invasive intratracheal instillation is a technique used to deliver substances directly into the lungs without surgical intervention.
An intradermal injection is administered into the dermis, the layer just beneath the epidermis, using a small-gauge needle at a shallow angle (10–15°).
Denature DNA at 95°C, anneal primers at 50-65°C, extend at 72°C using Taq polymerase, repeat for 25-40 cycles. Amplifies specific DNA sequences.
Hepatic portal vein (HPV) injection is a method used to deliver substances directly into the liver via the portal circulation.
