Marburg VSV Pseudovirus_RAVN strain GP with luciferase reporter
Catalog Number:
N31O81
Description:
This pseudotyped virus uses recombinant vesicular stomatitis virus (rVSV) to carry GP protein of Marburgvirus – Ravn (GenBank: DQ447649.1). As pseudovirus infectivity of rVSV without its original G is restricted to a single round of replication, the pseudotypes can be handled using BSL-2 containment practices. Infection of cells with this pseudotyped virus carrying luciferase reporter results in high level luciferase activity. See our titration result showing the undiluted pseudovirus (green) generates signal ~100,000-fold higher than uninfected control (cell alone as background in blue). We also evaluated the neutralizing activity of one published mAb called MR191 by using this pseudotyped virus with a HIV control mAb, see results.
Applications:
- Anti-Marburgvirus neutralizing antibody screening at high throughput
- Anti-Marburgvirus drug screening at high throughput
- Marburgvirus vaccine efficacy evaluation at high throughput
- Marburgvirus pseudovirus transduction of target cells for viral entry, receptor recognition, cellular tropism and functional studies, such as ADCC analysis
Biosafety Level:
Handle it in biosafety cabinet in BSL-2. Contacted tips & tubes should be decontaminated by 10% disinfecting bleach
Organism:
Marburgvirus -Related filovirus
Storage and shipping condition:
Shipping with dry ice. Require -80°C storage. Multiple freeze/Thaw cycles will reduce its sensitivity. Recommend only 1 cycle. Aliquot after the first thaw
Size:
200 μl with recommended 500-fold dilution. We recommend to use it at a dilution fold where the signal of pseudovirus infection is 1,000-fold higher than uninfected control (cell alone as background), although 100-1,000-fold high is acceptable. Can be used for 1,000 reactions (100 μl diluted virus) or 2,500 reactions if using reduced amount of pseudovirus (40 μl diluted virus).
Use protocol:
The complete protocol is shipped with the product.
Briefly, incubate 100 μl diluted virus with 100 μl your sample in each well of 96-well plate for 30-60 min at 37°C. Then add 100 μl target cells (Vero). Read luciferase signal next day. For protocol using reduced amount, incubate 40 μl diluted virus with 10 μl your sample in each well of 96-well plate for 30-60 min at 37°C. Then add 25 μl target cells. Add 150ul fresh media next day and read signal on Day 3.
Note:
- Pseudoviruses are intended for Research Use Only
- A positive control mAb is free with pseudovirus purchase
