Gå direkte til indholdet
Glatte muskelceller fra den menneskelige lungearterie (HPASMC)
Væv
Lung (pulmonary artery
Sygdom
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastasested
Not applicable (normal, non-tumorigenic primary cell)
Synonymer
HPASMC, Human pulmonary artery smooth muscle cells, provitro 1210613

Dokumenter

Glatte muskelceller fra den menneskelige lungearterie (HPASMC)

Primary cell · Varenummer 300706

Glat muskulatur fra lungekarrene til forskning i pulmonal arteriel hypertension (PAH)

€1,490.00ekskl. moms og fragt

Tilpasning / Anbefalinger

Fremstillet på bestilling
1

01Beskrivelse

02Generelle oplysninger

Beskrivelse

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.

Væv
Lung (pulmonary artery
Sygdom
Normal pulmonary arterial smooth muscle (non-tumorigenic primary cell)
Metastasested
Not applicable (normal, non-tumorigenic primary cell)
Anvendelser
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
Synonymer
  • HPASMC
  • Human pulmonary artery smooth muscle cells
  • provitro 1210613

03Donor

Donorens alder
Lot-specific (see CoA)
Etnisk tilhørsforhold
Lot-specific (see CoA)

04Klassificering

Organisme
Menneske
Køn
Partispecifik
Vækstegenskaber
Tilhænger
GMO-status
GMO-fri
Oplysninger om GMO-status
No genetic modification; primary human pulmonary artery smooth muscle cells isolated from normal pulmonary arteries. Not transformed or immortalized.
Biosikkerhedsniveau
1

05Egenskaber

Morfologi
Spindle-shaped (smooth muscle)
Celletype
Primary smooth muscle cells
Tumorfremkaldende
No
Fordoblingstid
Not specified by AddexBio; typical primary VSMC doubling time 36–72 hours

06Håndtering og opdræt

Næringsmedium
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubationsatmosfære

37°C, 5% CO2, saturated humidity.

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

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.

Opdelingsforhold
1 to 3
Såtæthed
More than 4,000 cells/cm²
Væskeudskiftning
24 hours after seeding, then every 48 to 72 hours
Genopretning efter optøning

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

Optøning og dyrkning
  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.

07Kvalitetskontrol og kryopræservering

Sterilitet

Mycoplasma contamination is excluded by PCR.

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

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

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.

Leveringsbetingelser

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

08Udtryk og modtagelighed

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

09Identifikatorer

Kildehenvisning
Human pulmonary artery smooth muscle cells (HPASMC) (Cytion catalog number 300706)
NCBI-skattenummer
9606
Cellosaurus
Not assigned

11Produktoplysninger

Sammensætningstabel