
- الأنسجة
- Bladder
- المرض
- Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
- موقع الانتشار
- Not applicable (normal, non-tumorigenic primary cell)
- المرادفات
- HBdSMC, HUSMC, Human urothelial smooth muscle cells, provitro 1210631
المستندات
خلايا العضلات الملساء الظهارية البولية البشرية (HUSMC)
Primary cell · رقم المنتج 300707
العضلات الملساء في المسالك البولية لأغراض أبحاث طب المسالك البولية
التخصيص / التوصيات
- خلايا العضلات الملساء الظهارية البولية البشرية (HUSMC)Primary cell€1,220.00
01الوصف
02معلومات عامة
- الوصف
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.
- الأنسجة
- Bladder
- المرض
- Normal bladder smooth muscle / detrusor (primary cells; non-tumorigenic)
- موقع الانتشار
- Not applicable (normal, non-tumorigenic primary cell)
- التطبيقات
- 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
- المرادفات
- HBdSMC
- HUSMC
- Human urothelial smooth muscle cells
- provitro 1210631
03المانح
- عمر المتبرع
- Lot-specific (see CoA)
- الأصل العرقي
- Lot-specific (see CoA)
04التصنيف
- كائن حي
- إنسان
- الجنس
- خاص بالقطعة
- خصائص النمو
- الملتزم
- حالة الكائنات المعدلة وراثيًا
- خالية من الكائنات المعدلة وراثيًا
- تفاصيل حالة الكائنات المعدلة وراثيًا
- No genetic modification; primary human bladder smooth muscle cells. Not transformed or immortalized. Confirmed negative for mycoplasma, bacteria, yeast, HIV-1, HBV, HCV.
- مستوى السلامة البيولوجية
- 1
05الخصائص
- المورفولوجيا
- Spindle-shaped (smooth muscle)
- نوع الخلية
- Primary smooth muscle cells
- مُسبِّب للأورام
- No
- زمن المضاعفة
- approx. 18 to 36 hours (lot-specific; AcceGen equivalent: ~13 population doublings guaranteed)
06التعامل مع النباتات وزراعتها
- وسط الاستزراع
- Smooth Muscle Cell Growth Medium kit (Cytion article number 850075); Smooth Muscle Cell Growth Medium mix (Cytion article number 850074)
- بيئة الحضانة
37°C, 5% CO2, saturated humidity.
- المكملات الغذائية
- 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.
- كاشف التفكك
- Subculture reagents as recommended on the certificate of analysis
- إعادة الاستنبات
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.
- نسبة التقسيم
- 1 to 3
- كثافة البذر
- More than 4,000 cells/cm²
- تجديد السوائل
- 24 hours after seeding, then every 48 to 72 hours
- التعافي بعد ذوبان الجليد
Post-thaw viability ≥ 70 % viable cells. More than 80 % confluence within the expected recovery period.
- إذابة الثلج والزراعة
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.
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.
Remove the supernatant and resuspend the cell pellet in 10 ml of Smooth Muscle Cell Growth Medium. Check cell number and viability.
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.
Incubate at 37 °C, 5 % CO₂ and saturated humidity, with the screw caps opened by half a turn for gas exchange.
Change the medium after 24 hours to remove unattached cells, then every 48 to 72 hours, using pre-warmed medium only.
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.
Recommended seeding density: more than 4,000 cells/cm².
07مراقبة الجودة والحفظ بالتبريد
- العقم
Mycoplasma contamination is excluded by PCR.
To ensure there is no bacterial, fungal or yeast contamination, cultures are subjected to visual inspection.
- وسط التجميد
- As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
- شروط التخزين
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.
- شروط الشحن
Cryopreserved primary cells are shipped on dry ice. On receipt, check the cryovial for damage and transfer it without delay to appropriate storage.
08التعبير والقابلية للإصابة
- المستضدات السطحية
- α-smooth muscle actin (α-SMA) +; Desmin +; Calponin (CNN1) +; SM-MHC (MYH11) + (differentiated); h-caldesmon + (differentiated); γ-smooth muscle actin + (differentiated); Connexin 43 +
- المستقبلات المُعبَّر عنها
- Muscarinic acetylcholine receptor M2 (CHRM2) +; Muscarinic receptor M3 (CHRM3) +; PDGFR-β (CD140b); Adrenergic receptors (β1, β3)
- الفيروسات
- Free of HIV-1, HBV, HCV (confirmed negative; AcceGen ABC-TC3862 QC)
09المعرّفات
- المرجع
- Human urothelial smooth muscle cells (HUSMC) (Cytion catalog number 300707)
- رقم التعريف الضريبي لدى NCBI
- 9606
- سيلوصور
- Not assigned
10الشؤون القانونية والسلامة
- احتياطات السلامة
- When planning to store a cryovial in liquid nitrogen for future thawing, it is mandatory to adhere to stringent safety measures. Appropriate protective gloves and clothing are essential, and the use of a face mask or safety goggles is required during the transfer of frozen samples to or from the liquid nitrogen tank. This is to mitigate the risk of injury from potential cryovial explosions upon removal, which can result in the projection of sharp fragments. Primary cells are of human origin, and no known test procedure can ensure the complete absence of infectious agents. Handle all products as potentially infectious.
- الضمان
At Cytion, we stand behind the quality and viability of our products. We guarantee that our cells will be viable at the start of culture for 60 days after shipment from our facilities. We assure that all materials conform to the specifications described in the Certificate of Analysis and/or Product Sheet.
For full details, please refer to our Warranty Statement.
- يلزم إبرام اتفاقية نقل المواد
- نعم
11تفاصيل المنتج
- جدول التركيب