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Cellule muscolari lisce uroteliali umane (HUSMC)
Tessuto
Bladder
Malattia
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Sito metastatico
Not applicable (normal, non-tumorigenic primary cell)
Sinonimi
HBdSMC, HUSMC, Human urothelial smooth muscle cells, provitro 1210631

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Cellule muscolari lisce uroteliali umane (HUSMC)

Primary cell · Codice prodotto 300707

Muscolatura liscia delle vie urinarie per la ricerca urologica

€1,220.00IVA e spese di spedizione escluse

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01Descrizione

02Informazioni generali

Descrizione

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.

Tessuto
Bladder
Malattia
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Sito metastatico
Not applicable (normal, non-tumorigenic primary cell)
Applicazioni
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
Sinonimi
  • HBdSMC
  • HUSMC
  • Human urothelial smooth muscle cells
  • provitro 1210631

03Donatore

Età dei donatori
Lot-specific (see CoA)
Etnia
Lot-specific (see CoA)

04Classificazione

Organismo
Umano
Sesso
Specifico per lotto
Proprietà di crescita
Aderente
Presenza di OGM
Senza OGM
Dettagli sullo stato degli OGM
No genetic modification; primary human bladder smooth muscle cells. Not transformed or immortalized. Confirmed negative for mycoplasma, bacteria, yeast, HIV-1, HBV, HCV.
Livello di biosicurezza
1

05Caratteristiche

Morfologia
Spindle-shaped (smooth muscle)
Tipo di cellula
Primary smooth muscle cells
Tumorigenico
No
Tempo di raddoppio
approx. 18 to 36 hours (lot-specific; AcceGen equivalent: ~13 population doublings guaranteed)

06Manipolazione e coltura

Terreno di coltura
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Atmosfera di incubazione

37°C, 5% CO2, saturated humidity.

Integratori
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.
Reagente di dissociazione
Subculture reagents as recommended on the certificate of analysis
Subcoltura

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.

Rapporto di frazionamento
1 to 3
Densità di semina
More than 4,000 cells/cm²
Rinnovo dei fluidi
24 hours after seeding, then every 48 to 72 hours
Recupero post-scongelamento

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

Scongelamento e coltura
  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.

07Controllo di qualità e crioconservazione

Sterilità

Mycoplasma contamination is excluded by PCR.

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

Terreno di coltura congelato
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Condizioni di conservazione

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.

Condizioni di spedizione

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

08Espressione e suscettibilità

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

09Identificatori

Riferimento bibliografico
Human urothelial smooth muscle cells (HUSMC) (Cytion catalog number 300707)
Codice fiscale NCBI
9606
Cellosaurus
Not assigned

11Dettagli sul prodotto

Tabella delle composizioni