Siirry sisältöön
Ihmisen uroteelisolujen sileät lihassolut (HUSMC)
Kudos
Bladder
Sairaus
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Metastaasikohde
Not applicable (normal, non-tumorigenic primary cell)
Synonyymit
HBdSMC, HUSMC, Human urothelial smooth muscle cells, provitro 1210631

Asiakirjat

Ihmisen uroteelisolujen sileät lihassolut (HUSMC)

Primary cell · Tuotenumero 300707

Virtsateiden sileälihas urologisen tutkimuksen tarpeisiin

€1,220.00ilman veroja ja toimituskuluja

Räätälöinti / Suositukset

Valmistetaan tilauksesta
1

01Kuvaus

02Yleistä tietoa

Kuvaus

Primary Human Bladder Smooth Muscle Cells (HBdSMC) are isolated from the smooth muscle layer of the urinary tract. They are used to study the response of the bladder wall to mechanical stretch and as a building block for engineered bladder tissue.

HBdSMC respond to cyclic stretch and hydrostatic pressure that mimic bladder filling with increased proliferation and altered contractility, involving muscarinic receptor signaling. This makes them a model for detrusor remodeling in bladder outlet obstruction and for conditioning cells in bladder tissue engineering.

Kudos
Bladder
Sairaus
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Metastaasikohde
Not applicable (normal, non-tumorigenic primary cell)
Sovellukset
Cyclic stretch of the bladder wall, muscarinic receptors and proliferation; Hydrostatic pressure in bladder outlet obstruction: proliferation and contractility; Hypoxia and oxidative stress in bladder ischemia; Rac1 signaling as a target in overactive bladder; Bladder tissue engineering with urothelial and smooth muscle cells
Synonyymit
  • HBdSMC
  • HUSMC
  • Human urothelial smooth muscle cells
  • provitro 1210631

03Lahjoittaja

Luovuttajan ikä
Lot-specific (see CoA)
Etnisyys
Lot-specific (see CoA)

04Luokittelu

Organismi
Ihminen
Sukupuoli
Tonttikohtainen
Kasvuominaisuudet
Kiinnittynyt
GMO-status
GMO-vapaa
GMO-statuksen tiedot
No genetic modification; primary human bladder smooth muscle cells. Not transformed or immortalized. Confirmed negative for mycoplasma, bacteria, yeast, HIV-1, HBV, HCV.
Bioturvallisuustaso
1

05Ominaisuudet

Morfologia
Spindle-shaped (smooth muscle)
Solutyyppi
Primary smooth muscle cells
Kasvaimia aiheuttava
No
Kaksinkertaistumisaika
approx. 18 to 36 hours (lot-specific; AcceGen equivalent: ~13 population doublings guaranteed)

06Käsittely ja viljely

Viljelyalusta
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubaatioilma

37°C, 5% CO2, saturated humidity.

Ravintolisät
Supplement per AcceGen medium kit instructions. Standard SMC growth medium contains FBS (5–10%), EGF, FGF, and insulin as major components. Refer to product-specific CoA.
Dissosiaatioreagenssi
Subculture reagents as recommended on the certificate of analysis
Soluviljely

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.

Jakosuhde
1 to 3
Kylvötiheys
More than 4,000 cells/cm²
Nesteen uusiminen
24 hours after seeding, then every 48 to 72 hours
Sulamisen jälkeinen palautuminen

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

Sulatus ja viljely
  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.

07Laadunvalvonta ja kryosäilytys

Hedelmättömyys

Mycoplasma contamination is excluded by PCR.

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

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

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.

Toimitusehdot

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

08Ilmentyminen ja alttius

Pinta-antigeenit
α-smooth muscle actin (α-SMA) +; Desmin +; Calponin (CNN1) +; SM-MHC (MYH11) + (differentiated); h-caldesmon + (differentiated); γ-smooth muscle actin + (differentiated); Connexin 43 +
Ilmentyvät reseptorit
Muscarinic acetylcholine receptor M2 (CHRM2) +; Muscarinic receptor M3 (CHRM3) +; PDGFR-β (CD140b); Adrenergic receptors (β1, β3)
Virukset
Free of HIV-1, HBV, HCV (confirmed negative; AcceGen ABC-TC3862 QC)

09Tunnisteet

Lähdeviite
Human urothelial smooth muscle cells (HUSMC) (Cytion catalog number 300707)
NCBI-verotunnus
9606
Cellosaurus
Not assigned

11Tuotetiedot

Koostumustaulukko