abm | RFP Stably Expressing HEK293 Cell Line (Safe Harbor Site) | T3700

abm | RFP Stably Expressing HEK293 Cell Line (Safe Harbor Site) | T3700

HEK293 cells stably expressing RFP using CRISPR Knock In Technology at the Safe Harbor Site (AAVS1)

Biosafety:

II

Organism:

Human

Source Organ:

Kidney

Growth Properties:

Adherent

Morphology:

Polygonal

Clones:

N/A

Passage Number:

N/A

Population Doner:

N/A

Seeding Density:

30,000 - 40,000 cells/cm², Recommended Split ratio of 1:2 to 1:4

Markers:

Puromycin

Applications:

N/A

Doner Gender:

N/A

Donor Ethnicity:

N/A

Knockdown Method:

N/A

Induction:

N/A

Overexpression:

N/A

Freeze Thaw:

1. Pre-warm complete media in a 37°C waterbath.
2. Remove the cryopreserved vial from the liquid nitrogen storage tank.
3. Thaw the cells quickly by placing the lower half of the vial into the 37°C water bath and remove after 60 seconds. There should still be a few ice crystals left after thawing. It is important not to over-thaw the cryovials as the presence of DMSO is toxic to the cells.
4. Re-suspend the cells in the vial and transfer the cell suspension into a 15mL sterile conical tube containing 5mL complete media.
5. Centrifuge cells at 200x g for 3 minutes to pellet.
6. Aspirate out the media, leaving cell pellet undisturbed.
7. Re-suspend pellet in fresh culture medium and plate in new culture vessel.
8. Incubate cultures at 37°C, 5% CO₂.
T3700 may show the presence of several floating cells after thawing. Within 48-72 hours these cells should revive.

Propagation:

The base medium for this cell line is Prigrow III medium available at abm

Preservation:

N/A

Quality Control:

1) Puromycin drug selection.
2) RFP fluorescence expression

Tumorgenicn:

N/A

Shipping Conditions:

Dry Ice

Storage Contidions:

-180°C