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Please note that this cell line is not available under a standard Cytion MTA, as it requires a third-party agreement and/or is subject to negotiation with the original licensor. Contact us if you are interested in ordering this cell line.
| Item number | Size | Datasheet | Manual | SDS | Delivery time | Quantity | Price |
|---|---|---|---|---|---|---|---|
| CYT-300294 | 1 each | - |
6 - 10 business days* |
800.00€
|
If you have any questions, please use our Contact Form.
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
Categories: Reporter-labeled cells Description: The U-2 OS-ZFN-SNAP-Nup107 cell line represents a... more
Product information "U2OS-ZFN-SNAP-Nup107 Cells"
Categories: Reporter-labeled cells Description: The U-2 OS-ZFN-SNAP-Nup107 cell line represents a specialized variant of the widely used human osteosarcoma cell line U-2 OS. This particular model has been engineered to express the SNAP-tagged version of the nucleoporin Nup107, a pivotal component of the nuclear pore complex, which is essential for the transport of molecules between the nucleus and the cytoplasm. The integration of the SNAP-tag technology allows for the biorthogonal labeling and visualization of Nup107 in live or fixed cells, providing a powerful tool for studying nucleocytoplasmic transport and nuclear pore complex architecture under physiological conditions. The U-2 OS background offers several advantages, including robust growth rates and a well-characterized karyotype, which support high-throughput screening applications and genomic studies. The ZFN (Zinc Finger Nuclease) technology used in this cell line facilitates targeted genome editing, enhancing the precision with which researchers can investigate the genetic contributions to nuclear transport and other cellular processes. This cell line is particularly useful for studies aimed at elucidating the dynamics and regulation of nuclear pore complexes in cancer biology and cellular physiology. Due to the specialized nature of the U-2 OS-ZFN-SNAP-Nup107 no.294 cell line, it is highly suited for advanced imaging techniques, including super-resolution microscopy, to explore nucleoporin functions at unprecedented detail. It is also a valuable resource for developing therapeutic strategies targeting nuclear transport pathways implicated in various diseases, including cancer. The SNAP-tag component adds versatility for further biochemical and proteomic analyses, making it an indispensable tool in the field of cellular and molecular biology. Organism: Human Tissue: Bone Disease: Osteosarcoma Age: 15 years Gender: Female Ethnicity: Caucasian Growth Properties: Adherent Citation: U-2 OS-ZFN-SNAP-Nup107 (Cytion catalog number 300294) Biosafety Level: 1 Ncbi_ Taxid: 9606.0 Cellosaurus Accession: CVCL_B7FM Protein Expression: SNAP-Nup107 (nuclear pore complex protein 107, SNAP-tag) Culture Medium: McCoys 5a, w: 3.0 g/L Glucose, w: stable Glutamine, w: 2.0 mM Sodium pyruvate, w: 2.2 g/L NaHCO3 (Cytion article number 820200a) Supplements: Supplement the medium with 10% FBS, 3.0 g/L Glucose, stable Glutamine, 2.0 mM Sodium pyruvate, 2.2 g/L NaHCO3, 1% NEAA Dissociation Reagent: Accutase Subculturing: Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium. Fluid Renewal: 2 to 3 times per week Freeze Medium: As a cryopreservation medium, use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress. Thawing And Culturing Cells: Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks, for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes. Sterility: Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. Safety Precautions: When planning to store a cryovial in liquid nitrogen for future thawing, it is mandatory to adhere to stringent safety measures. Appropriate protective gloves and clothing are essential, and the use of a face mask or safety goggles is required during the transfer of frozen samples to or from the liquid nitrogen tank. This is to mitigate the risk of injury from potential cryovial explosions upon removal, which can result in the projection of sharp fragments. Warranty: We stand by the promise of delivering products with high cell viability and robust culture performance. To achieve the best results, please make sure you follow the storage and culture instructions detailed in the product information sheet closely. Your adherence to these guidelines is key to success. Subject To Third- Party Agreements: Please note that this cell line is not available under a standard Cytion MTA, as it requires a third-party agreement and/or is subject to negotiation with the original licensor. Required Product 1: 820200a Required Product 3: 860015.0 Required Product 4: 830100.0
| Supplier: | Cytion |
| Supplier-Nr: | 300294 |
Properties
| Species reactivity: | human |
Database Information
Handling & Safety
| Storage: | Liquid nitrogen |
| Shipping: | -80°C (International: -80°C) |
Caution
Our products are for laboratory research use only: Not for administration to humans!
Our products are for laboratory research use only: Not for administration to humans!
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