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Gewebe
Ovary
Krankheit
Chinese hamster ovary, non-neoplastic; genetically engineered for CXCR7 (ACKR3) surface expression (medium-high expression level)
Synonyme
CHO-CXCR7

Dokumente

CHO-CXCR7 Mittel bis hoch

Cell line · Artikelnummer 305412MH

Haftungsausschluss: Die für Zelllinien angegebenen Preise gelten ausschließlich für Kunden aus dem akademischen Bereich bzw. gemeinnützige Einrichtungen. Für kommerzielle Unternehmen gelten die Preise...

€5,000.00zzgl. MwSt. und Versandkosten
Auftragsfertigung
1

01Allgemeine Informationen

Beschreibung

Disclaimer: The prices displayed for cell lines are exclusively for academic/not-for-profit customers. For commercial entitites the price is approximately €6,250.
If you represent a commercial entity or are unsure which category applies, please contact us.


The CHO-CXCR7-Medium-high cell line is a stable recombinant CHO (Chinese Hamster Ovary) cell line engineered to express the CXCR7 receptor at a medium-high level. This cell line was created using an innovative landing pad technology, which allows for targeted integration of the CXCR7 gene at a pre-validated genomic locus, ensuring consistent and reproducible expression. CXCR7, also known as ACKR3, is an atypical chemokine receptor involved in immune modulation and cancer biology. Unlike typical GPCRs, CXCR7 does not signal through G proteins but instead scavenges chemokines such as CXCL12 and CXCL11, and forms heterodimers with CXCR4, influencing processes like tumor progression, metastasis, and angiogenesis.

CXCR7 is notably overexpressed in various cancers, including breast, lung, and prostate cancers, where it is linked to increased tumor growth, metastasis, and poorer prognosis. This makes the CHO-CXCR7-Medium-high cell line particularly valuable for oncology research, allowing for the study of CXCR7's role in cancer progression and its potential as a therapeutic target. The expression of CXCR7 in this cell line was confirmed using flow cytometry.

Gewebe
Ovary
Krankheit
Chinese hamster ovary, non-neoplastic; genetically engineered for CXCR7 (ACKR3) surface expression (medium-high expression level)
Anwendungen
Antibody screening; CXCR7-targeted therapy development; chemokine receptor biology; tumor microenvironment research; flow cytometry
Synonyme
  • CHO-CXCR7

02Klassifizierung

Organismus
Chinesischer Hamster
Sex
Weiblich
Wachstumseigenschaften
Adhärente und Suspension
GVO-Status
GMO-S1
Angaben zum GVO-Status
GMO-S1: This CHO cell line contains a construct supporting medium-to-high expression of human CXCR7 for chemokine receptor research. This classification applies only within Germany and may differ elsewhere.
Biologische Sicherheitsstufe
1

03Merkmale

Morphologie
Epithelial-like
Zelltyp
Epithelial cells
Verdopplungszeit
approx. 14-16 hours

04Bezeichner

Quellenangabe
CHO-CXCR7 Medium-high (Cytion catalog number 305412MH)
NCBI-Steuer-ID
10029
Cellosaurus
CVCL_A8W2

05Expression und Anfälligkeit

Exprimierte Rezeptoren
CXCR7 (ACKR3)

06Handhabung und Kultur

Nährmedium

For adherent cultures: DMEM:Ham's F12 (1:1), w: 3.1 g/L Glucose, w: 2.5 mM L-Glutamine, w: 15 mM HEPES, w: 0.5 mM Sodium pyruvate, w: 1.2 g/L NaHCO3 (Cytion article number 820400a)

For suspension cultures: CHO Growth Medium A (from InSCREENeX; InSCREENeX catalog number INS-ME-1039)

Inkubationsatmosphäre

37°C, 5% CO2, humidified atmosphere.

Nahrungsergänzungsmittel
For adherent cultures: Supplement the medium with 5% FBS. Add Geneticin (G418-Sulfat) to achieve a final concentration of 0.5 mg/mL.
Dissoziationsreagenz
For adherent cultures: Trypsin-EDTA
Subkultivierung
For routine adherent cell culture: Aspirate the old culture medium from the adherent cells, and wash them with PBS to remove any remaining medium. After aspirating the PBS, add the appropriate volume of Trypsin/EDTA solution based on the culture vessel size (e.g., 1 ml for a T25 flask, 3 ml for a T75 flask) and incubate at room temperature or 37°C for 5-10 minutes, or until the cells detach. Monitor detachment under a microscope, and gently tap the vessel if necessary to release the cells. Once detached, add complete medium to inactivate the Trypsin/EDTA, gently resuspend the cells, and transfer an aliquot of the cell suspension into a new culture vessel containing fresh medium. Place the vessel in an incubator set to 37°C with 5% CO2, and change the medium every 2-3 days.
Split-Verhältnis
1 to 5
Aussaatdichte
2 to 5 x 104 cells/cm2
Flüssigkeitswechsel
2 to 3 times per week
Erholung nach dem Auftauen

After thawing, split the cells at a ratio of 1:2 to 1:3 in T25 flasks and allow the cells to recover from the freezing process and to adhere (for adherent cultures) for at least 24 hours.

Auftauen und Kultivierung
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

07Qualitätskontrolle und Kryokonservierung

Sterilität

Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods.

To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections.

Gefriermedium
As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
Lagerbedingungen

For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.

Versandbedingungen

Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.

08Spender

Alter des Spenders
Adult