CHO-K1 Human CCR10 Cell Line

CHO-K1 Human CCR10 Cell Line

Cat. No: RQP71355

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 CHO-K1 stable cell line that stably expresses tag-free human CCR10 receptor. Upon agonist binding to CCR10, the Gi-type G protein signaling pathway is activated, inhibiting adenylyl cyclase and triggering a decrease in intracellular cAMP concentration. Therefore, receptor activity can be easily quantified in live cells in a dose-response manner by measuring changes in cAMP levels. This cell line is suitable for HTS and receptor functional evaluation assays.

Schematic diagram of CCR10 signaling pathway. CCL27 binds CCR10, activates Gαi, inhibits adenylate cyclase and reduces cAMP.

Figure 1. Schematic diagram of the CCR10 CHO-K1 cell model

Assay Principle

HTRF‑cAMP assay schematic diagram, GPCR live‑cell compound stimulation, cAMP detection via FRET for dose‑response quantification

Cells are stimulated with test compounds to modulate intracellular cAMP levels. The resulting cAMP changes are then detected through a competitive immunoassay format, and receptor activity is quantified by dose-response analysis. 

Cat. No RQP71355
Product Name CHO-K1 Human CCR10 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 F12K+10%FBS+5μg/ml puromycin
Freeze Medium 90% FBS+10% DMSO
Storage Conditions Liquid nitrogen immediately upon delivery
Transducer Gi
Application Functional assay for CCR10
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 Chemokine receptors
Sub Family Class A (Rhodopsin)
Gene Name CCR10
Gene Aliases GPR2
Gene ID 2826
Accession Number NM_001293
UniProt Number P46092
Protein Name C-C motif chemokine receptor 10
Protein Aliases C-C chemokine receptor type 10;CCR-10;G protein-coupled receptor 2
Target Species Human
Host cell CHO-K1

Flow cytometry histogram comparing CCR10 expression on CCR10 / CHO-K1 cells and parental CHO-K1 cells.Figure 1. Recombinant CCR10/CHO-K1 constitutively expressing CCR10

The CCR10/CHO-K1 cells (blue curve) showed high fluorescence intensity with Mean FL4-A = 2.55E5, while parental CHO-K1 cells (red curve) exhibited negligible signal (Mean FL4-A = 663). The result confirms high and stable expression of human CCR10 receptor on cell membrane.

HTRF cAMP assay dose-response curve of CCR10 CHO cells stimulated by CCL27, EC50 = 23 nM.

Figure 2. HTRF cAMP Assay with CCR10 CHO-K1(C5)

CCL27 induced a dose-dependent response with EC50 = 23 nM, verifying specific receptor activity of CCR10, suitable for compound screening and pharmacological characterization.

 

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 CCR10 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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