CHO-K1 Human TCRα/β-CD3 complex&CD4 Cell

CHO-K1 Human TCRα/β-CD3 complex&CD4 Cell

Cat. No: RQP74499

Size: 1 vial of frozen cells (>1E6 per vial in 1 mL)

Unit Price: Contact For Pricing

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Product Info
Description
Biological Information
Cell Culture
Cat. No RQP74499
Product Name CHO-K1 Human TCRα/β-CD3 complex&CD4 Cell
Product Type Expression Cell line
Culture Properties Adherent
Stability 32passages (in-house test, that not means the cell line will be instable beyond the passages we tested.)
Mycoplasma Status Negative
Culture Medium F12K+10% FBS + 5μg/ml Puromycin +600μg/ml Hygromycin B + 5μg/ml Blasticidin
Freeze Medium 90% FBS+10% DMSO
Storage Conditions Liquid nitrogen immediately upon delivery
Application Binding Assay,FACS

 

 

For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.

  

CHO-K1 cell line expressing full length Human TCRα/β-CD3 complex&CD4 Cell.Expression is confirmed by flow cytometry.

Figure 1. Recombinant TCRα/β-CD3 complex&CD4 CHO stably expressing TCRα/β.

Figure 2. Recombinant TCRα/β-CD3 complex&CD4 CHO stably expressing CD4.

Figure 3. Recombinant TCRα/β-CD3 complex&CD4 CHO stably expressing CD3.

 

Cell Resuscitation
1)Rapidly thaw the frozen cells in a 37 °C water bath for approximately 60 seconds. Once thawed (which may take slightly less or more than 60 seconds), immediately transfer the cell suspension from the cryovial into a 15 mL centrifuge tube containing 10 mL of pre-warmed  CHO-K1 Human TCRα/β-CD3 complex&CD4 Cell complete culture medium.
2)Centrifuge cells at 1000 rpm for 5 min to remove medium, then resuspend cells in 5 mL of pre-warmed complete medium.
3)Transfer the cell suspension into a T25 culture flask and incubate at 37 °C with 5% CO₂.
4)After approximately 24–36 hours, replace the medium or passage the cells to remove non-adherent dead cells.


Subculturing procedure
1)When the cell density reaches the appropriate confluency for passaging, wash the cells with PBS, then add 1 mL trypsin to detach the cells. When more than 80% of the cells detach upon gently tapping the culture flask, add complete culture medium to terminate digestion. Gently pipette to obtain a single-cell suspension, transfer to a 15 mL centrifuge tube, and centrifuge at 1000 rpm for 5 minutes.

2)Discard supernatant after centrifugation. Resuspend cells in fresh medium to a single-cell suspension and transfer to a new culture flask for continued growth.


Cell Freezing
After trypsinization and centrifugation of cells from each T75 flask or 10 cm culture dish, discard the supernatant. Add 2 mL of cryopreservation medium (90% FBS + 10% DMSO), gently resuspend thoroughly, and aliquot into two cryovials. Immediately place the cryovials into a controlled-rate freezing container (e.g., Nalgene 5100-0001), fill with isopropanol to the indicated level, and store at −80 °C. After 24 hours, transfer the cryovials to liquid nitrogen for long-term storage.

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