
- Tessuto
- Lung (pulmonary artery
- Malattia
- Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
- Sito metastatico
- Not applicable (normal, non-tumorigenic primary cell)
- Sinonimi
- HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613
Documenti
Cellule muscolari lisce dell'arteria polmonare umana (HPASMC)
Primary cell · Codice prodotto 300706
Muscolatura liscia vascolare polmonare per la ricerca sull’ipertensione arteriosa polmonare
Personalizzazione / Suggerimenti
- Cellule muscolari lisce dell'arteria polmonare umana (HPASMC)Primary cell€1,490.00
01Descrizione
02Informazioni generali
- Descrizione
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.
- Tessuto
- Lung (pulmonary artery
- Malattia
- Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
- Sito metastatico
- Not applicable (normal, non-tumorigenic primary cell)
- Applicazioni
- 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
- Sinonimi
- HPASMC
- Human pulmonary artery smooth muscle cells
- provitro 1210613
03Donatore
- Età dei donatori
- Lot-specific (see CoA)
- Etnia
- Lot-specific (see CoA)
04Classificazione
- Organismo
- Umano
- Sesso
- Specifico per lotto
- Proprietà di crescita
- Aderente
- Presenza di OGM
- Senza OGM
- Dettagli sullo stato degli OGM
- No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
- Livello di biosicurezza
- 1
05Caratteristiche
- Morfologia
- Spindle-shaped (smooth muscle)
- Tipo di cellula
- Primary smooth muscle cells
- Tumorigenico
- No
- Tempo di raddoppio
- Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours
06Manipolazione e coltura
- Terreno di coltura
- Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
- Atmosfera di incubazione
37°C, 5% CO2, saturated humidity.
- Integratori
- Supplement as specified in the AddexBio SMC supplement kit (refer to specification sheet). For cryopreservation: complete culture medium + 5% (v/v) DMSO.
- Reagente di dissociazione
- Subculture reagents as recommended on the certificate of analysis
- Subcoltura
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.
- Rapporto di frazionamento
- 1 to 3
- Densità di semina
- More than 4,000 cells/cm²
- Rinnovo dei fluidi
- 24 hours after seeding, then every 48 to 72 hours
- Recupero post-scongelamento
Post-thaw viability ≥ 70 % viable cells. More than 80 % confluence within the expected recovery period.
- Scongelamento e coltura
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.
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.
Remove the supernatant and resuspend the cell pellet in 10 ml of Smooth Muscle Cell Growth Medium. Check cell number and viability.
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.
Incubate at 37 °C, 5 % CO₂ and saturated humidity, with the screw caps opened by half a turn for gas exchange.
Change the medium after 24 hours to remove unattached cells, then every 48 to 72 hours, using pre-warmed medium only.
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.
Recommended seeding density: more than 4,000 cells/cm².
07Controllo di qualità e crioconservazione
- Sterilità
Mycoplasma contamination is excluded by PCR.
To ensure there is no bacterial, fungal or yeast contamination, cultures are subjected to visual inspection.
- Terreno di coltura congelato
- As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
- Condizioni di conservazione
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.
- Condizioni di spedizione
Cryopreserved primary cells are shipped on dry ice. On receipt, check the cryovial for damage and transfer it without delay to appropriate storage.
08Espressione e suscettibilità
- Espressione proteica
- Smooth muscle α-actin; calponin; smooth muscle myosin heavy chain
- Virus
- Free of HIV, Hepatitis B, Hepatitis C (confirmed negative by AddexBio)
09Identificatori
- Riferimento bibliografico
- Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
- Codice fiscale NCBI
- 9606
- Cellosaurus
- Not assigned
10Aspetti legali e di sicurezza
- Misure di sicurezza
- When planning to store a cryovial in liquid nitrogen for future thawing, it is mandatory to adhere to stringent safety measures. Appropriate protective gloves and clothing are essential, and the use of a face mask or safety goggles is required during the transfer of frozen samples to or from the liquid nitrogen tank. This is to mitigate the risk of injury from potential cryovial explosions upon removal, which can result in the projection of sharp fragments. Primary cells are of human origin, and no known test procedure can ensure the complete absence of infectious agents. Handle all products as potentially infectious.
- Garanzia
At Cytion, we stand behind the quality and viability of our products. We guarantee that our cells will be viable at the start of culture for 60 days after shipment from our facilities. We assure that all materials conform to the specifications described in the Certificate of Analysis and/or Product Sheet.
For full details, please refer to our Warranty Statement.
- È richiesto un accordo di trasferimento di materiale
- Sì
11Dettagli sul prodotto
- Tabella delle composizioni