Tartalomra ugrás
Emberi pulmonális artéria simaizomsejtek (HPASMC)
Szövet
Lung (pulmonary artery
Betegség
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Áttétes hely
Not applicable (normal, non-tumorigenic primary cell)
Szinonimák
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Dokumentumok

Emberi pulmonális artéria simaizomsejtek (HPASMC)

Primary cell · Termékszám 300706

Tüdőérrendszeri simaizomsejtek a pulmonális artériás hipertenzió (PAH) kutatásához

€1,490.00adó és szállítási költség nélkül

Személyre szabás / Ajánlások

Rendelésre készül
1

01Leírás

02Általános információk

Leírás

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.

Szövet
Lung (pulmonary artery
Betegség
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Áttétes hely
Not applicable (normal, non-tumorigenic primary cell)
Alkalmazások
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
Szinonimák
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Adományozó

Az adományozó életkora
Lot-specific (see CoA)
Etnikai hovatartozás
Lot-specific (see CoA)

04Osztályozás

Organizmus
Ember
Szex
Tétel-specifikus
Növekedési tulajdonságok
Hűséges
GMO-státusz
GMO-mentes
A GMO-státuszra vonatkozó részletek
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Biológiai biztonsági szint
1

05Jellemzők

Morfológia
Spindle-shaped (smooth muscle)
Sejttípus
Primary smooth muscle cells
Daganatképző
No
Kettőzési idő
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Kezelés és tenyésztés

Táptalaj
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubációs környezet

37°C, 5% CO2, saturated humidity.

Kiegészítők
Supplement as specified in the AddexBio SMC supplement kit (refer to specification sheet). For cryopreservation: complete culture medium + 5% (v/v) DMSO.
Diszociációs reagens
Subculture reagents as recommended on the certificate of analysis
Átültetés

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.

Osztási arány
1 to 3
Ültetési sűrűség
More than 4,000 cells/cm²
Folyadékcsere
24 hours after seeding, then every 48 to 72 hours
Az olvadás utáni helyreállás

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

Felolvasztás és tenyésztés
  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.

07Minőségellenőrzés és kriokonzerválás

Meddőség

Mycoplasma contamination is excluded by PCR.

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

Fagyasztóközeg
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Tárolási feltételek

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.

Szállítási feltételek

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

08Kifejeződés és fogékonyság

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

09Azonosítók

Hivatkozás
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
NCBI adóazonosító szám
9606
Cellosaurus
Not assigned

11Termékadatok

Összetételi táblázat