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Ad5/RGD-Luciferase Chimeric Adenovirus

Ad5/RGD-Luciferase Chimeric Adenovirus

Cat.No. :  AD18656Z

Titer: ≥1x10^10 IFU/mL / ≥1x10^11 IFU/mL / ≥1x10^11 VP/mL / ≥1x10^12 VP/mL Size: 100 ul/500 ul/1 mL

Storage:  -80℃ Shipping:  Frozen on dry ice

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Adenovirus Particle Information

Quality Control

Cat. No. AD18656Z
Description Fiber modified Ad5/RGD chimeric adenoviral particles which express luciferase reporter gene.
Target Gene Luciferase
Titer Varies lot by lot, for example, ≥1x10^10 IFU/mL, ≥1x10^11 IFU/mL, ≥1x10^11 VP/mL etc.
Size Varies lot by lot, for example, 250 ul, 500 ul, 1 mL etc.
Storage Store at -80℃. Avoid multiple freeze/thaw cycles.
Shipping Frozen on dry ice
Creative Biogene ensures high-quality adenovirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between adenovirus particle lots.
Endotoxin Endotoxins, primarily derived from Gram-negative bacteria, can trigger adverse immune responses. Endotoxin contamination is a significant concern in adenovirus production, especially for applications in animal studies and gene therapy. Creative Biogene utilizes rigorous endotoxin detection methods to monitor the endotoxin level in our produced adenovirus particles to ensure regulatory compliance.
Sterility Creative Biogene ensures that adenovirus products are free of any bacterial, fungal and other microbial contamination.
Ad5 E1 Detection All Creative Biogene adenoviruses are PCR tested to ensure that there are no detectable E1 sequences in the particles, which could be from revertants or external E1 contamination.
RCA Assays Adenovirus products originating at Creative Biogene are guaranteed to have undetectable replication-competent adenovirus (RCA). This quality control measure is important because there is always the possibility of wild-type contamination due to revertants or environmental sources.
PFU Titering All purified adenovirus preparations are tested for infectious titer. Creative Biogene's PFU test takes a few days longer but counts true plaques in HEK cells rather than estimating PFU titers via IHC staining or TCI50 of infected cells.
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Ad5/RGD-luciferase chimeric adenovirus is a genetically engineered viral vector that utilizes an alternative cell entry pathway to enhance gene delivery. This vector possesses a modified fibrin sphere in which an arginine-glycine-aspartic acid (RGD) peptide motif is inserted into the HI loop of the Ad5 fibrin. This modification allows the adenovirus to bypass the need for Coxsackievirus and adenovirus receptor (CAR) and instead bind directly to αvβ3 and αvβ5 integrins on the surface of target cells. These integrins are widely expressed in various cell types, including vascular endothelial cells, certain tumor cells, and immune cells such as dendritic cells, which typically exhibit low CAR expression levels. The vector is non-replicating and carries a firefly luciferase reporter gene, enabling highly sensitive and quantitative detection of gene expression via bioluminescence assays.

The application of Ad5/RGD-luciferase chimeric adenovirus is significant in immunological and vascular biology research. It is commonly used to transduce dendritic cells for cancer immunotherapy research. Compared to standard Ad5 vectors, RGD-integrin interactions enhance gene transfer efficiency, leading to better expression of immunomodulatory factors. In the laboratory, luciferase reporter genes can sensitively detect the distribution and persistence of gene expression in in vitro cell cultures and in vivo animal models. Researchers have used this system to track viral tropism in different tissues and evaluate the effectiveness of integrin-targeted therapies in tumor growth and angiogenesis. Furthermore, the Ad5/RGD platform is a valuable tool for optimizing viral delivery protocols and conducting high-throughput drug screening to modulate transduction efficiency or cellular responses to viral infection.
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Customer Reviews
Excellent Transduction Efficiency!

The RGD modification significantly improved the transduction efficiency of our CAR-low cells. The luciferase signal is robust and reliable, allowing for in vivo imaging.

Germany

07/12/2021

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