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Lidské uroteliální buňky hladkého svalstva (HUSMC)
Tkáň
Bladder
Nemoc
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Místo metastázy
Not applicable (normal, non-tumorigenic primary cell)
Synonyma
HBdSMC, HUSMC, Human urothelial smooth muscle cells, provitro 1210631

Dokumenty

Lidské uroteliální buňky hladkého svalstva (HUSMC)

Primary cell · Číslo výrobku 300707

Hladké svalstvo močových cest pro urologický výzkum

€1,220.00bez DPH a poštovného

Přizpůsobení / Doporučení

Na zakázku
1

01Popis

02Obecné informace

Popis

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.

Tkáň
Bladder
Nemoc
Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
Místo metastázy
Not applicable (normal, non-tumorigenic primary cell)
Aplikace
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
Synonyma
  • HBdSMC
  • HUSMC
  • Human urothelial smooth muscle cells
  • provitro 1210631

03Dárce

Věk dárce
Lot-specific (see CoA)
Etnická příslušnost
Lot-specific (see CoA)

04Klasifikace

Organismus
Člověk
Sex
Specifické pro danou šarži
Růstové vlastnosti
Přívrženec
Stav GMO
Bez GMO
Podrobnosti o 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.
Úroveň biologické bezpečnosti
1

05Charakteristika

Morfologie
Spindle-shaped (smooth muscle)
Typ buňky
Primary smooth muscle cells
Tumorogenní
No
Doba zdvojnásobení
approx. 18 to 36 hours (lot-specific; AcceGen equivalent: ~13 population doublings guaranteed)

06Manipulace a chov

Pěstovací médium
Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
Inkubační atmosféra

37°C, 5% CO2, saturated humidity.

Doplňky stravy
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.
Disociační činidlo
Subculture reagents as recommended on the certificate of analysis
Subkultivace

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.

Poměr rozdělení
1 to 3
Hustota výsevu
More than 4,000 cells/cm²
Obnova tekutin
24 hours after seeding, then every 48 to 72 hours
Zotavení po rozmrazení

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

Rozmrazování a kultivace
  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 kvality a kryokonzervace

Sterilita

Mycoplasma contamination is excluded by PCR.

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

Mrazicí médium
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
Podmínky skladování

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.

Dopravní podmínky

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

08Exprese a náchylnost

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

09Identifikátory

Citace
Human urothelial smooth muscle cells (HUSMC) (Cytion catalog number 300707)
Daňové identifikační číslo NCBI
9606
Cellosaurus
Not assigned

11Podrobnosti o produktu

Tabulka složení