الانتقال إلى المحتوى
الأنسجة
Ovary
المرض
Chinese hamster ovary, non-neoplastic; genetically engineered for CXCR4 surface expression (medium-high expression level)
المرادفات
CHO-CXCR4

المستندات

CHO-CXCR4 متوسط إلى مرتفع

Cell line · رقم المنتج 305411MH

إخلاء المسؤولية: الأسعار المعروضة للخطوط الخلوية مخصصة حصريًّا للعملاء الأكاديميين أو غير الهادفين للربح. أما بالنسبة للكيانات التجارية، فإن الأسعار...

€5,000.00باستثناء الضريبة وتكاليف الشحن
حسب الطلب
1

01معلومات عامة

الوصف

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-CXCR4-Medium-high cell line is a stable recombinant CHO (Chinese Hamster Ovary) cell line expressing the CXCR4 receptor at a medium-high level, approximately 9500 molecules per cell. This cell line was developed using an innovative landing pad technology, which ensures targeted integration of the CXCR4 gene at a pre-validated genomic locus. This approach results in consistent and reliable expression of the CXCR4 receptor, facilitating reproducible experimental outcomes.

CXCR4, also known as CD184, is a chemokine receptor involved in critical biological processes such as immune cell trafficking, hematopoiesis, and as a co-receptor for HIV entry into cells. The receptor's interaction with its ligand, CXCL12, is essential for the migration and homing of hematopoietic stem cells and leukocytes. In oncology, CXCR4 plays a significant role in tumor growth, metastasis, and angiogenesis, with its expression often upregulated in various cancers, including hematological malignancies. This upregulation is frequently associated with therapy resistance and poor prognosis. The expression of CXCR7 in this cell line was confirmed using flow cytometry.

الأنسجة
Ovary
المرض
Chinese hamster ovary, non-neoplastic; genetically engineered for CXCR4 surface expression (medium-high expression level)
التطبيقات
Antibody screening; CXCR4-targeted therapy development; HIV entry research; hematopoietic stem cell biology; flow cytometry
المرادفات
  • CHO-CXCR4

02التصنيف

كائن حي
الهامستر الصيني
الجنس
أنثى
خصائص النمو
التثبيت والتعليق
حالة الكائنات المعدلة وراثيًا
GMO-S1
تفاصيل حالة الكائنات المعدلة وراثيًا
GMO-S1: This CHO derivative contains a construct driving medium-to-high expression of human CXCR4 for GPCR signaling and ligand-binding analyses. This classification applies only within Germany and may differ elsewhere.
مستوى السلامة البيولوجية
1

03الخصائص

المورفولوجيا
Epithelial-like
نوع الخلية
Epithelial cells
زمن المضاعفة
approx. 14-16 hours

04المعرّفات

المرجع
CHO-CXCR4 Medium-high (Cytion catalog number 305411MH)
رقم التعريف الضريبي لدى NCBI
10029
سيلوصور
CVCL_A8W0

05التعبير والقابلية للإصابة

المستقبلات المُعبَّر عنها
CXCR4 (CD184)

06التعامل مع النباتات وزراعتها

وسط الاستزراع

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)

بيئة الحضانة

37°C, 5% CO2, humidified atmosphere.

المكملات الغذائية
For adherent cultures: Supplement the medium with 5% FBS. Add Geneticin (G418-Sulfat) to achieve a final concentration of 0.5 mg/mL.
كاشف التفكك
For adherent cultures: Trypsin-EDTA
إعادة الاستنبات
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.
نسبة التقسيم
1 to 5
كثافة البذر
2 to 5 x 104 cells/cm2
تجديد السوائل
2 to 3 times per week
التعافي بعد ذوبان الجليد

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.

إذابة الثلج والزراعة
  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.

07مراقبة الجودة والحفظ بالتبريد

العقم

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.

وسط التجميد
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.
شروط التخزين

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.

شروط الشحن

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.

08المانح

عمر المتبرع
Adult

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