Mine otse sisu juurde
Inimese kopsuarteri silelihasrakud (HPASMC)
Kude
Lung (pulmonary artery
Haigus
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastaaside asukoht
Not applicable (normal, non-tumorigenic primary cell)
Sünonüümid
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Dokumendid

Inimese kopsuarteri silelihasrakud (HPASMC)

Primary cell · Toote number 300706

Kopsu veresoonte silelihas PAH-uuringuteks

€1,490.00ilma käibemaksu ja saatmiskuludeta

Kohandamine / Soovitused

Tellimusel valmistatud
1

01Kirjeldus

02Üldine teave

Kirjeldus

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.

Kude
Lung (pulmonary artery
Haigus
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastaaside asukoht
Not applicable (normal, non-tumorigenic primary cell)
Rakendused
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
Sünonüümid
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Annetaja

Doonori vanus
Lot-specific (see CoA)
Etniline kuuluvus
Lot-specific (see CoA)

04Klassifikatsioon

Organism
Inimene
Sugu
Kogupõhine
Kasvuvõime
Järgija
GMO-staatus
GMO-vaba
GMO-staatuse üksikasjad
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Bioloogilise ohutuse tase
1

05Omadused

Morfoloogia
Spindle-shaped (smooth muscle)
Rakutüüp
Primary smooth muscle cells
Tuumorigeenne
No
Kahekordistumisaeg
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Käsitlemine ja kasvatamine

Kasvatuskeskkond
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubatsiooni keskkond

37°C, 5% CO2, saturated humidity.

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

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.

Jagamissuhe
1 to 3
Külvitihedus
More than 4,000 cells/cm²
Vedeliku vahetus
24 hours after seeding, then every 48 to 72 hours
Taastumine pärast sulamist

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

Sulatamine ja kasvatamine
  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.

07Kvaliteedikontroll ja krüokonserveerimine

Viljatus

Mycoplasma contamination is excluded by PCR.

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

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

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.

Tarne- ja kohaletoimetamistingimused

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

08Avaldumine ja vastuvõtlikkus

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

09Tunnused

Viide
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
NCBI maksukood
9606
Cellosaurus
Not assigned

11Toote üksikasjad

Koostis tabel