Przejdź do treści
Ludzkie komórki mięśni gładkich nabłonka układu moczowego (HUSMC)
Chusteczka
Bladder
Choroba
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Miejsce przerzutów
Not applicable (normal, non-tumorigenic primary cell)
Synonimy
HBdSMC, HUSMC, Human urothelial smooth muscle cells, provitro 1210631

Dokumenty

Ludzkie komórki mięśni gładkich nabłonka układu moczowego (HUSMC)

Primary cell · Numer produktu 300707

Mięśnie gładkie dróg moczowych do badań urologicznych

€1,220.00bez podatku i kosztów wysyłki

Dostosowanie / Zalecenia

Wykonane na zamówienie
1

01Opis

02Informacje ogólne

Opis

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.

Chusteczka
Bladder
Choroba
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Miejsce przerzutów
Not applicable (normal, non-tumorigenic primary cell)
Zastosowania
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
Synonimy
  • HBdSMC
  • HUSMC
  • Human urothelial smooth muscle cells
  • provitro 1210631

03Darczyńca

Wiek dawcy
Lot-specific (see CoA)
Pochodzenie etniczne
Lot-specific (see CoA)

04Klasyfikacja

Organizm
Człowiek
Seks
Specyficzne dla partii
Właściwości związane ze wzrostem
Zwolennik
Status GMO
Bez GMO
Szczegółowe informacje dotyczące statusu GMO
No genetic modification; primary human bladder smooth muscle cells. Not transformed or immortalized. Confirmed negative for mycoplasma, bacteria, yeast, HIV-1, HBV, HCV.
Poziom bezpieczeństwa biologicznego
1

05Cechy charakterystyczne

Morfologia
Spindle-shaped (smooth muscle)
Typ komórki
Primary smooth muscle cells
Nowotworotwórczy
No
Czas podwojenia
approx. 18 to 36 hours (lot-specific; AcceGen equivalent: ~13 population doublings guaranteed)

06Postępowanie i hodowla

Pożywka hodowlana
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Atmosfera inkubacyjna

37°C, 5% CO2, saturated humidity.

Suplementy
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.
Odczynnik dysocjacyjny
Subculture reagents as recommended on the certificate of analysis
Hodowla komórek w subkulturze

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.

Współczynnik podziału
1 to 3
Gęstość wysiewu
More than 4,000 cells/cm²
Odnawianie płynów
24 hours after seeding, then every 48 to 72 hours
Powrót do stanu sprzed rozmrożenia

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

Rozmrażanie i hodowla
  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.

07Kontrola jakości i kriokonserwacja

Bezpłodność

Mycoplasma contamination is excluded by PCR.

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

Pożywka do zamrażania
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Warunki przechowywania

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.

Warunki wysyłki

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

08Ekspresja i podatność

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

09Identyfikatory

Źródło
Human urothelial smooth muscle cells (HUSMC) (Cytion catalog number 300707)
Numer identyfikacji podatkowej NCBI
9606
Cellosaurus
Not assigned

11Szczegóły produktu

Tabela składu