
- Tecido
- Lung (pulmonary artery
- Doença
- Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
- Local da metástase
- Not applicable (normal, non-tumorigenic primary cell)
- Sinónimos
- HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613
Documentos
Células do músculo liso da artéria pulmonar humana (HPASMC)
Primary cell · Número do produto 300706
Músculo liso vascular pulmonar para investigação sobre a HAP
Personalização / Recomendações
- Células do músculo liso da artéria pulmonar humana (HPASMC)Primary cell€1,490.00
01Descrição
02Informações gerais
- Descrição
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.
- Tecido
- Lung (pulmonary artery
- Doença
- Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
- Local da metástase
- Not applicable (normal, non-tumorigenic primary cell)
- Aplicações
- 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
- Sinónimos
- HPASMC
- Human pulmonary artery smooth muscle cells
- provitro 1210613
03Doador
- Idade do dador
- Lot-specific (see CoA)
- Etnia
- Lot-specific (see CoA)
04Classificação
- Organismo
- Humano
- Sexo
- Específico do lote
- Propriedades de crescimento
- Aderente
- Estatuto em matéria de OGM
- Sem OGM
- Detalhes sobre o estatuto dos OGM
- No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
- Nível de biossegurança
- 1
05Características
- Morfologia
- Spindle-shaped (smooth muscle)
- Tipo de célula
- Primary smooth muscle cells
- Tumorigénico
- No
- Tempo de duplicação
- Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours
06Manuseamento e cultura
- Meio de cultura
- Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
- Atmosfera de incubação
37°C, 5% CO2, saturated humidity.
- Suplementos
- Supplement as specified in the AddexBio SMC supplement kit (refer to specification sheet). For cryopreservation: complete culture medium + 5% (v/v) DMSO.
- Reagente de dissociação
- Subculture reagents as recommended on the certificate of analysis
- Subcultura
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.
- Rácio de divisão
- 1 to 3
- Densidade de sementeira
- More than 4,000 cells/cm²
- Renovação de fluidos
- 24 hours after seeding, then every 48 to 72 hours
- Recuperação após o descongelamento
Post-thaw viability ≥ 70 % viable cells. More than 80 % confluence within the expected recovery period.
- Descongelamento e cultura
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.
07Controlo de qualidade e criopreservação
- Esterilidade
Mycoplasma contamination is excluded by PCR.
To ensure there is no bacterial, fungal or yeast contamination, cultures are subjected to visual inspection.
- Meio de congelação
- As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
- Condições de armazenamento
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.
- Condições de envio
Cryopreserved primary cells are shipped on dry ice. On receipt, check the cryovial for damage and transfer it without delay to appropriate storage.
08Expressão e suscetibilidade
- Expressão proteica
- Smooth muscle α-actin; calponin; smooth muscle myosin heavy chain
- Vírus
- Free of HIV, Hepatitis B, Hepatitis C (confirmed negative by AddexBio)
09Identificadores
- Referência
- Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
- Número de identificação fiscal do NCBI
- 9606
- Cellosaurus
- Not assigned
10Aspectos legais e de segurança
- Precauções de segurança
- 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.
- Garantia
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.
- É necessário um Acordo de Transferência de Material
- Sim
11Detalhes do produto
- Tabela de composição