HEK293 Human CCK2R Cell Line

HEK293 Human CCK2R Cell Line

Cat. No: RQP71608

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

Unit Price: Contact For Pricing

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Description

Product Info

Biological Info

Assay Data

Cell Culture

 

This product is a HEK293 stable cell line that stably expresses tag-free human CCK2R receptor. Upon agonist binding to CCK2R, the Gq-type G protein signaling pathway is activated, stimulating PLC and triggering an increase in intracellular Ca²⁺ and IP1 concentration. Therefore, receptor activity can be easily quantified in live cells in a dose-response manner by measuring changes in IP1 or calcium levels. This cell line is suitable for high-throughput screening (HTS) and receptor functional evaluation assays.

Schematic diagram of CCK2R signaling pathway. Sincalide binds CCK2R, activates Gαq-PLC pathway, increases IP1 and intracellular Ca²⁺.

Figure 1. Schematic diagram of the CCK2R HEK293 cell model

Assay Principle

IP1‑HTRF assay schematic diagram, live‑cell IP1 accumulation inhibited by LiCl, competitive TRF detection for GPCR dose‑response quantification

This schematic shows the IP1 time-resolved fluorescence assay for Gq GPCR detection. Agonist activates Gq signaling to raise cellular IP1. LiCl inhibits IP1 breakdown. Cellular IP1 competes with labeled tracer for anti‑IP1 antibody binding. Time-resolved fluorescence signals are measured to build dose-response curves and quantify receptor activity.

Cat. No RQP71608
Product Name HEK293 Human CCK2R Cell Line
Engineering method plasmid transfection
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 DMEM+10%FBS+2 μg/ml Puromycin
Freeze Medium 90% FBS+10% DMSO
Storage Conditions Liquid nitrogen immediately upon delivery
Transducer Gq
Application

Functional assay for CCK2R

Safety Precautions

Wear lab coat, disposable gloves to avoid direct sample contact.

For spills: apply disinfectant, allow full inactivation, then clean up.

Seal samples properly during transportation to prevent leakage and biological contamination.

 

 

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

Target Class GPCR
Family Cholecystokinin receptors
Sub Family Class A(Rhodopsin)
Gene Name CCKBR
Gene Aliases CCK2R; GASR; CCK-BR; CCK-2R
Gene ID 887
Accession Number NM_176875
UniProt Number P32239
Protein Name Cholecystokinin receptor type B; CCK-B receptor; CCK-BR
Protein Aliases CCK2-R
Target Species Human
Host cell HEK293

HTRF IP-One Assay with CCK2R HEK293Dose-response curve of HTRF IP-One assay: Sincalide stimulates CCK2R HEK293 cells, EC50=0.12 nM; parental cells show no obvious response.(C1)

Figure 1. HTRF IP-One Assay with CCK2R HEK293(C1)

Sincalide induced a dose‑dependent inhibitory response in CCK2R-expressing cells with EC50 = 0.12 nM, while parental HEK293 cells showed no obvious response (EC50 > 200 nM), confirming specific Gq-mediated CCK2R receptor activity.

 

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 HEK293 Human CCK2R Cell Line 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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