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Human GDF7 adenoviral particles

Human GDF7 adenoviral particles

Cat.No. :  AD00176Z

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

Gene Informationn

Cat. No. AD00176Z
Target Gene GDF7
Species Human
Product Type Adenoviral particle
Insert GDF7
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.
Gene Name
Gene Symbol
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Gene Description
Gene ID
UniProt ID
mRNA Refseq
Protein Refseq
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MIM
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Growth differentiation factor 7 (GDF7), also known as bone morphogenetic protein 12 (BMP12), is a member of the transforming growth factor beta (TGF-β) superfamily. This secreted signaling protein plays a crucial role in embryonic development, tissue homeostasis, and regeneration. GDF7 is particularly known for its involvement in the differentiation and maintenance of connective tissues, including tendons, ligaments, and cartilage. Studies have shown that it promotes the formation of tendon-like structures and enhances the repair of musculoskeletal injuries. The GDF7 gene encodes a precursor protein that is proteolytically cleaved to release the mature, biologically active dimer. Due to its potent osteogenic and chondrogenic properties, GDF7 has attracted much attention in the fields of regenerative medicine, orthopedic research, and gene therapy applications. Human GDF7 adenoviral particles are engineered viral vectors designed to efficiently deliver the GDF7 gene to target cells or tissues. These particles are based on adenovirus, a non-enveloped DNA virus known for its high transduction efficiency, broad tropism, and ability to infect both dividing and non-dividing cells. Adenoviral vectors carrying the GDF7 gene enable stable transient expression of the protein, making them a valuable tool for research in tissue engineering, wound healing, and musculoskeletal repair. These particles are often produced using advanced packaging cell lines to ensure high titer and purity, while their safety features, such as replication deficiency, minimize risk in experimental settings. Researchers have used these particles to study the therapeutic potential of GDF7 in preclinical models, including tendon injury, osteoarthritis, and spinal cord regeneration.
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Customer Reviews
Excellent specificity

These Human GDF7 adenoviral particles provided strong, localized expression in neural progenitor cells without the broad effects seen with other BMPs. The particles were potent and delivered exactly the phenotype we aimed for. Excellent specificity.

United States

06/16/2022

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