Jurkat E6.1 Human CD27/NFκB-Luc Cell

Jurkat E6.1 Human CD27/NFκB-Luc Cell

Cat. No: RQP74007

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
Assay Data
Cell Culture
Cat. No RQP74007
Product Name Jurkat E6.1 Human CD27/NFκB-Luc Cell
Product Type Reporter Cell
Culture Properties suspension
Stability 32passages (in-house test, that not means the cell line will be instable beyond the passages we tested.)
Mycoplasma Status Negative
Culture Medium RPMI-1640+10%FBS+800μg/ml Hygromycin B+1μg/ml puromycin
Freeze Medium 90% FBS+10% DMSO
Storage Conditions Liquid nitrogen immediately upon delivery
Application Functional(Report Gene) Assay

 

 

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

 

Recombinant Jurkat T cell expressing firefly luciferase gene under the control of NF-kB response elements with constitutive expression of human CD27 (also known as Tumor Necrosis Factor Receptor Superfamily Member 7, TNFRSF7, and T14 .

Figure 1. Recombinant CD27/NFκB-Luc/Jurkat E6.1 stably expressing CD27.

Classification Co-Stimulatory
Family Tumor necrosis factor receptor superfamily CD molecules
Gene Name CD27
Gene Aliases TNFRSF7;S152;Tp55
Gene ID 939
Accession Number NM_001242.5
UniProt Number P26842
Protein Name CD27 antigen
Protein Aliases CD27L receptor;T-cell activation antigen CD27;T14;Tumor necrosis factor receptor superfamily member 7
Target Species Human
Host cell Jurkat E6.1

    

Figure 2.  Detect Luciferase assay by Ultra Luciferase Detection Kit RQPH0001(we strongly suggest to purchase from Reqbio). CD27/Jurkat NFκB-Luc(Clone 2) report assay stimulated by CD70/CHO cells.

 

Cell Passage Procedures

1.This cell line grows in suspension.
2.Upon receipt, cells should be thawed immediately or stored in liquid nitrogen until use.
3.Before thawing, pre-warm the water bath and culture medium to 37 °C, and prepare a small amount of dry ice.
4.Remove the cryovial from storage and transport it to the cell culture laboratory on dry ice.
5.Rapidly thaw the cells in a 37 °C water bath. Once the cells are completely thawed, spray the cryovial with 70% ethanol for disinfection and transfer it to a biosafety cabinet.
6.Add 10 mL of pre-warmed culture medium into a 15 mL centrifuge tube. Transfer the contents of the cryovial into the tube and centrifuge at 1000 rpm for 5 minutes.
7.Carefully discard the supernatant. Resuspend the cell pellet in 5 mL of pre-warmed culture medium by gentle pipetting. Immediately perform cell counting and adjust the cell density to 3–6 × 10⁵ cells/mL based on the counting results, then transfer the cells into a culture flask.
8.Count the cells every 1–2 days. When the cell density exceeds 1 × 10⁶ cells/mL, passage the cells promptly or add fresh culture medium. Maintain the cell density between 2 × 10⁵ and 1 × 10⁶ cells/mL.


Suspension Cell Cryopreservation Procedure:

1.Collect 8 × 10⁶ cells, centrifuge, and discard the supernatant.
2.Add 1 mL of cell freezing medium (90% FBS + 10% DMSO) and gently pipette to mix thoroughly. Transfer the suspension into a cryovial.
3.Immediately place the cryovial into a controlled-rate freezing container (Nalgene 5100-0001), fill with isopropanol up to the indicated level, and store at −80 °C.
4.After 24 hours, transfer the cryovial to liquid nitrogen for long-term storage.

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