الانتقال إلى المحتوى
خلايا العضلات الملساء للشريان الرئوي البشري (HPASMC)
الأنسجة
Lung (pulmonary artery
المرض
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
موقع الانتشار
Not applicable (normal, non-tumorigenic primary cell)
المرادفات
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

المستندات

خلايا العضلات الملساء للشريان الرئوي البشري (HPASMC)

Primary cell · رقم المنتج 300706

العضلات الملساء الوعائية الرئوية لأغراض أبحاث ارتفاع ضغط الدم الرئوي

€1,490.00باستثناء الضريبة وتكاليف الشحن

التخصيص / التوصيات

حسب الطلب
1

01الوصف

02معلومات عامة

الوصف

Primary Human Pulmonary Artery Smooth Muscle Cells (HPASMC) are isolated from the pulmonary artery. They are a key model for pulmonary arterial hypertension, including hypoxia-driven proliferation and vascular remodeling.

Hypoxia drives the proliferation of HPASMC, and PDGF-BB shifts them toward a synthetic, migratory phenotype, reproducing key features of pulmonary vascular remodeling. Because the balance of BMP and TGF-β signaling is central to pulmonary arterial hypertension, the cells are also used to study BMPR2-related mechanisms.

الأنسجة
Lung (pulmonary artery
المرض
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
موقع الانتشار
Not applicable (normal, non-tumorigenic primary cell)
التطبيقات
Pulmonary arterial hypertension: BMP/TGF-β balance, proliferation and migration; Hypoxia-induced proliferation, PPARγ and microRNA-21; Long non-coding RNA regulation of migration in pulmonary arterial hypertension; Functional testing of BMPR2 promoter variants in reporter assays; PDGF-BB-induced phenotype switching and metabolomics; Endothelin-1 signaling and proteomics of BMPR2-mutant cells
المرادفات
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03المانح

عمر المتبرع
Lot-specific (see CoA)
الأصل العرقي
Lot-specific (see CoA)

04التصنيف

كائن حي
إنسان
الجنس
خاص بالقطعة
خصائص النمو
الملتزم
حالة الكائنات المعدلة وراثيًا
خالية من الكائنات المعدلة وراثيًا
تفاصيل حالة الكائنات المعدلة وراثيًا
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
مستوى السلامة البيولوجية
1

05الخصائص

المورفولوجيا
Spindle-shaped (smooth muscle)
نوع الخلية
Primary smooth muscle cells
مُسبِّب للأورام
No
زمن المضاعفة
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06التعامل مع النباتات وزراعتها

وسط الاستزراع
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
بيئة الحضانة

37°C, 5% CO2, saturated humidity.

المكملات الغذائية
Supplement as specified in the AddexBio SMC supplement kit (refer to specification sheet). For cryopreservation: complete culture medium + 5% (v/v) DMSO.
كاشف التفكك
Subculture reagents as recommended on the certificate of analysis
إعادة الاستنبات

Subculture the cells at about 75 % confluence. Denser cultures undergo irreversible contact inhibition and stop proliferating. Use the subculture reagents recommended on the certificate of analysis.

نسبة التقسيم
1 to 3
كثافة البذر
More than 4,000 cells/cm²
تجديد السوائل
24 hours after seeding, then every 48 to 72 hours
التعافي بعد ذوبان الجليد

Post-thaw viability ≥ 70 % viable cells. More than 80 % confluence within the expected recovery period.

إذابة الثلج والزراعة
  1. Thaw the cryovial quickly in a 37 °C water bath, swirling gently. Just before the last ice has melted, move the vial to a laminar flow hood and decontaminate its outer surface.

  2. Transfer the cell suspension into a 15 ml centrifuge tube, add 10 ml of Smooth Muscle Cell Growth Medium and centrifuge at 250 × g for 5 minutes.

  3. Remove the supernatant and resuspend the cell pellet in 10 ml of Smooth Muscle Cell Growth Medium. Check cell number and viability.

  4. Divide the suspension between two 25 cm² culture flasks (5 ml each). Using two flasks reduces the risk of losing all cells if a passage fails.

  5. Incubate at 37 °C, 5 % CO₂ and saturated humidity, with the screw caps opened by half a turn for gas exchange.

  6. Change the medium after 24 hours to remove unattached cells, then every 48 to 72 hours, using pre-warmed medium only.

  7. Subculture the cells at about 75 % confluence. Denser cultures undergo irreversible contact inhibition and stop proliferating. Use the subculture reagents recommended on the certificate of analysis.

  8. Recommended seeding density: more than 4,000 cells/cm².

07مراقبة الجودة والحفظ بالتبريد

العقم

Mycoplasma contamination is excluded by PCR.

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

وسط التجميد
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
شروط التخزين

For long-term preservation, store vials in liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable for up to one week only.

شروط الشحن

Cryopreserved primary cells are shipped on dry ice. On receipt, check the cryovial for damage and transfer it without delay to appropriate storage.

08التعبير والقابلية للإصابة

التعبير البروتيني
Smooth muscle α-actin; calponin; smooth muscle myosin heavy chain
الفيروسات
Free of HIV, Hepatitis B, Hepatitis C (confirmed negative by AddexBio)

09المعرّفات

المرجع
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
رقم التعريف الضريبي لدى NCBI
9606
سيلوصور
Not assigned

11تفاصيل المنتج

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