NRK-4xlambdaN22-3xmEGFP-M9 cell

SKU:BHC11101335
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Overview
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NRK-4xlambdaN22-3xmEGFP-M9 cell is a cell line. It is commonly used as an in vitro model for 1 research. Growth characteristics: Monolayer, adherent, Fibroblast-like cells with fusiform shape. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Rat
Morphology Fibroblast-like cells with fusiform shape
Growth Properties Monolayer, adherent
Tissue Kidney
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Catalog no. Size
500672 1 cryovial
Available Options

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 500672
Species Rat
The NRK-4xlambdaN22-3xmEGFP-M9 cell line is a clonal stable cell line derived from normal rat kidney (NRK) cells through the transfection of a circular plasmid. This plasmid contains genetic constructs encoding four tandem repeats of lambda N22 RNA-binding sites and three tandem repeats of mEGFP (monomeric enhanced green fluorescent protein) tags fused with the M9 nuclear localization signal. Post-transfection, the cells underwent drug resistance selection to ensure the stability of the genetic modifications. Approximately 50% of the cells in this clonal stable line express the fluorescent marker 4xλN22-3xmEGFP-M9, indicating successful incorporation of the plasmid. The expression of this marker allows for real-time visualization of intracellular processes, facilitated by the robust fluorescent signal of mEGFP. The M9 nuclear localization signal ensures that the expressed fusion proteins are transported to the nucleus, making this cell line particularly useful for studying nuclear-cytoplasmic transport, RNA dynamics, and gene expression regulation. This NRK-4xlambdaN22-3xmEGFP-M9 cell line is valuable for researchers focusing on RNA-binding protein interactions, RNA metabolism, and the mechanisms underlying nuclear import and export. The presence of the mEGFP marker enables advanced imaging techniques such as confocal microscopy and live-cell imaging, providing detailed insights into the spatial and temporal dynamics of cellular components. Despite the variegation, the cell line remains a powerful tool for dissecting complex molecular pathways and understanding cellular functions at a deeper level.

SKU:BHC11101335

  • Receptors expressed: Epidermal growth factor (EGF), multiplication stimulating activity (MSA)
  • Protein expression: 4xλN22-3xmEGFP-M9: Location/Gene: 937..1009, 1066..1138, 1194..1261, 1323..1390 / lambda peptide, 1462..2176, 2179..2890, 2896..3612 / mEGFP, 3612..3815 / M9-His, 5090..5884 / KanR/NeoR, 7195..584 / Pcmv
  • Products: M9-His tag between BsrG1/HindIII, Neomycin, Phosphotransferase, CMV Promotor
  • cultureMedium: 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)
  • supplements: Supplement the medium with 10% FBS, 0.5 mg/mL G418
  • dissociationReagent: Accutase
  • subculturing: Discard the old medium and wash the cells with PBS. Add a freshly prepared 0.025% trypsin/0.02% EDTA solution heated to 37 degrees Celsius and wait until the cells detach, which usually takes about 5 minutes. Neutralize the trypsin by adding fresh medium, then transfer the cell mixture to a tube and centrifuge. After centrifugation, remove the supernatant, resuspend the cell pellet in fresh culture medium, and transfer the suspension to new flasks. Incorporate G418 into the culture medium to achieve a final concentration of 0.5 mg/ml
  • seedingDensity: 2 to 4 x 104 cells/cm2
  • 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.
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