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Human FZD7 adenoviral particles

Human FZD7 adenoviral particles

Cat.No. :  AD00173Z

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. AD00173Z
Target Gene FZD7
Species Human
Product Type Adenoviral particle
Insert FZD7
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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The frizzled class receptor 7 (FZD7) gene encodes a member of the Frizzled family of proteins, which are key receptors in the Wnt signaling pathway. These pathways play key roles in embryonic development, tissue homeostasis, and cell proliferation, differentiation, and polarity. FZD7 is a seven-transmembrane domain protein that binds to Wnt ligands to initiate both canonical (β-catenin-dependent) and non-canonical (β-catenin-independent) signaling cascades. Dysregulation of FZD7 has been implicated in a variety of cancers, including colorectal, breast, and hepatocellular carcinomas, and its overexpression is often associated with tumor progression, metastasis, and poor prognosis. Due to its central role in the Wnt signaling pathway, FZD7 has emerged as a potential therapeutic target. Human FZD7 adenoviral particles are non-replicating viral vectors designed to efficiently deliver the FZD7 gene to mammalian cells. These particles take advantage of the natural ability of adenoviruses to infect a variety of cell types, both dividing and non-dividing, ensuring stable gene expression. The adenoviral backbone has been modified to eliminate pathogenic genes, improving safety while maintaining high transduction efficiency. After infection, the delivered FZD7 transgene is integrated into the host cell's transcriptional machinery, supporting overexpression studies to explore the role of FZD7 in Wnt signaling, cancer biology, or regenerative medicine. Researchers use these particles to explore the effects of FZD7 on behaviors such as cell migration, invasion, and stem cell properties, and to screen potential inhibitors. In addition, they can also serve as a platform for gene therapy development, especially for diseases associated with Wnt pathway dysfunction.
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Customer Reviews
Excellent Tool

We've been struggling to achieve stable Wnt pathway activation in primary cells. Creative Biogene's human FZD7 adenoviral particles were exactly what we needed. They delivered high titers, excellent transduction efficiency, and clear overexpression results—exactly what we needed to test our hypothesis.

Canada

07/06/2020

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