HK-CRISPR-mEGFP-Nup214 Cells
1 104,00 CAD$*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
Renseignements généraux
| Description | The HK-CRISPR-mEGFP-Nup214 cell line is designed to study Nup214, a key nuclear pore complex (NPC) component. Using CRISPR-Cas9, this cell line adds a monomeric enhanced green fluorescent protein (mEGFP) tag to Nup214, allowing real-time visualization of its role in nucleocytoplasmic transport and cell cycle regulation. This cell line ensures minimal off-target effects and enables advanced imaging techniques to study NPC structure and function. It is valuable for investigating nucleocytoplasmic transport and related diseases, such as certain leukemias, and is useful for screening compounds that affect NPC function. |
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| Organisme | Human |
| Tissu | Endocervix |
| Maladie | Adenocarcinoma |
Caractéristiques
| Âge | 30 years |
|---|---|
| Genre | Female |
| Origine ethnique | African American |
| Morphologie | Epithelial-like cells with mosaic stone shape |
| Propriétés de croissance | Adherent |
Données réglementaires
| Référence | HK-CRISPR-mEGFP-Nup214 (Cytion catalog number 300671) |
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| Niveau de biosécurité | 1 |
| NCBI_Numéro d'identification fiscale | 9606 |
| Déposant | The Ellenberg Lab (EMBL) |
| Statut OGM | GMO-S1: This HeLa Kyoto line contains a CRISPR-engineered mEGFP fusion at the Nup214 locus for studying nucleocytoplasmic transport. This classification applies only within Germany and may differ elsewhere. |
Données biomoléculaires
| Expression des protéines | Nup214, mEGFP-tag |
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Manipulation
| Milieu de culture | DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a) |
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| Suppléments | Supplement the medium with 10% FBS |
| Réactif de dissociation | Accutase |
| Repiquage | 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. |
| Milieu de congélation | As a cryopreservation medium, we 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. |
| Décongélation et culture des cellules |
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| Atmosphère d'incubation | 37°C, 5% CO2, humidified atmosphere. |
| Conditions d'expédition | Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage. |
| Conditions d'entreposage | For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen. |
Contrôle de la qualité et analyse moléculaire
| Stérilité | 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. |
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Certificat d'analyse (CoA)
| Numéro de lot | Type de certificat | Date | Numéro de catalogue |
|---|---|---|---|
| 300671-170924 | Certificat d'analyse | 23. May. 2025 | 300671 |