U2OS-ZFN-SNAP-Nup107 cell

SKU:BHC11100880
Bulk Pricing Research Validated
Overview
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U2OS-ZFN-SNAP-Nup107 cell is a cell line derived from Caucasian (Female). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Osteosarcoma
Growth Properties Adherent
Tissue Bone
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Catalog no. Size
300294 1 cryovial
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This cell line is available in the U.S. For non-profit users, please sign and submit the Non-Profit Supply Agreement to orders@biohippo.com before placing an order. For commercial users, please complete the CLEAR Form before ordering, as additional usage fees may apply based on the intended use. For further details, please contact orders@biohippo.com. Products ship after the required agreement is completed; typical delivery is 2–3 business days. Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10^6 cells for adherent lines or 5 × 10^6 cells for suspension lines (refer to the batch CoA for details).

Field Specification
Mfr No 300294
Species Human
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.

SKU:BHC11100880

Protein expression: SNAP-Nup107 (nuclear pore complex protein 107, SNAP-tag)

  • cultureMedium: 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
  • dissociationReagent: 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.
  • fluidRenewal: 2 to 3 times per week
  • freezeMedium: 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.
  1. Photon-free (s)CMOS camera characterization for artifact reduction in high- and super-resolution microscopyNature Communications| DOI: 10.1038/s41467-022-30907-2 | PMID: 35690614 | PMC: pmc09188588
  2. Optimal Precision and Accuracy in 4Pi-STORM using Dynamic Spline PSF ModelsbioRxiv| DOI: 10.1101/2021.10.19.464803 | PMC: bio_rxiv__2021__10__19__464803
  3. A tubule-sheet continuum model for the mechanism of nuclear envelope assembly.Developmental cell| DOI: 10.1016/j.devcel.2023.04.003 | PMID: 37098350 | PMC: pm37098350
  4. Live-cell STED microscopy enables 50 nm resolution imaging with preserved cell proliferation.Scientific reports| DOI: 10.1038/s41598-026-48958-6 | PMID: 42049809 | PMC: pm42049809
  5. A general design of caging-group-free photoactivatable fluorophores for live-cell nanoscopyNature Chemistry| DOI: 10.1038/s41557-022-00995-0 | PMID: 35864152 | PMC: pmc09417988__41557_2022_995_MOESM2_ESM
  6. Optimal precision and accuracy in 4Pi-STORM using dynamic spline PSF modelsNature Methods| DOI: 10.1038/s41592-022-01465-8 | PMID: 35577958 | PMC: pmc09119851
  7. Accelerated MINFLUX Nanoscopy, through Spontaneously Fast-Blinking Fluorophores.Small (Weinheim an der Bergstrasse, Germany)| DOI: 10.1002/smll.202206026 | PMID: 36642798 | PMC: pm36642798
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