Přejít na obsah
Buňky hladkého svalstva lidské plicní tepny (HPASMC)
Tkáň
Lung (pulmonary artery
Nemoc
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Místo metastázy
Not applicable (normal, non-tumorigenic primary cell)
Synonyma
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Dokumenty

Buňky hladkého svalstva lidské plicní tepny (HPASMC)

Primary cell · Číslo výrobku 300706

Hladký sval plicních cév pro výzkum plicní arteriální hypertenze

€1,490.00bez DPH a poštovného

Přizpůsobení / Doporučení

Na zakázku
1

01Popis

02Obecné informace

Popis

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.

Tkáň
Lung (pulmonary artery
Nemoc
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Místo metastázy
Not applicable (normal, non-tumorigenic primary cell)
Aplikace
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
Synonyma
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Dárce

Věk dárce
Lot-specific (see CoA)
Etnická příslušnost
Lot-specific (see CoA)

04Klasifikace

Organismus
Člověk
Sex
Specifické pro danou šarži
Růstové vlastnosti
Přívrženec
Stav GMO
Bez GMO
Podrobnosti o statusu GMO
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Úroveň biologické bezpečnosti
1

05Charakteristika

Morfologie
Spindle-shaped (smooth muscle)
Typ buňky
Primary smooth muscle cells
Tumorogenní
No
Doba zdvojnásobení
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Manipulace a chov

Pěstovací médium
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubační atmosféra

37°C, 5% CO2, saturated humidity.

Doplňky stravy
Supplement as specified in the AddexBio SMC supplement kit (refer to specification sheet). For cryopreservation: complete culture medium + 5% (v/v) DMSO.
Disociační činidlo
Subculture reagents as recommended on the certificate of analysis
Subkultivace

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.

Poměr rozdělení
1 to 3
Hustota výsevu
More than 4,000 cells/cm²
Obnova tekutin
24 hours after seeding, then every 48 to 72 hours
Zotavení po rozmrazení

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

Rozmrazování a kultivace
  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.

07Kontrola kvality a kryokonzervace

Sterilita

Mycoplasma contamination is excluded by PCR.

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

Mrazicí médium
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Podmínky skladování

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.

Dopravní podmínky

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

08Exprese a náchylnost

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

09Identifikátory

Citace
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
Daňové identifikační číslo NCBI
9606
Cellosaurus
Not assigned

11Podrobnosti o produktu

Tabulka složení