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Immortalized Podocyte Progenitor Cell Line (UM51-Pre-Podo-hTERT)

SKU : BHC10902205

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Applied Biological Materials (abm) Inc.

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Mfr.No.	T0208
Description	The UM51-Pre-Podo-hTERT cell line was derived from progenitor cells isolated from the urine of a 51-year-old African male and immortalized using hTERT. These cells have been shown to proliferate indefinitely while retaining key podocyte characteristics.?M51-Pre-Podo-hTERT cells express several podocyte-specific markers, such as WT1, NPHS1, and SYNPO which are crucial for understanding the differentiation and functional capacity of podocytes. Despite continuous culture, the UM51-Pre-Podo-hTERT line maintains a stable morphology, proliferation capacity, and expression of critical podocyte markers. It also displays contact inhibition and P53 expression, suggesting maintained normal cellular controls. This cell line has been differentiated into mature podocytes and can enter the G0 phase, thus making it suitable for?tudying podocyte maturation and function, as well as for modeling diseases where podocyte quiescence and re-entry into the cell cycle play a role. Overall, the?M51-hTERT-Pre-Podo line is an excellent model for research studying nephrogenesis and kidney-associated diseases.
Cell Type	Immortalized Cells
Biosafety Level	2
Depositor	Renakbiotech
Disclaimer	1. All test parameters provided in the CoA are conducted using abm's standardized culture system and procedures. The stated values may vary under the end-user's culture conditions. Please verify that the product is suitable for your studies by referencing published papers or ordering RNA (0.5 ?g, Cat.# C207, $450.00) or cell lysate (100 ?g, Cat.# C206, $600.00) to perform preliminary experiments, or alternatively use our Gene Expression Assay Service (Cat# C138). All sales are final. 2. We recommend live cell shipments for ease of cell transfer and this option can be requested at the time of ordering. Please note that the end-user will need to evaluate the feasibility of live cell shipment by taking into account the final destination's temperature variation and its geographical location. In addition, we thoroughly test our cell lines for freeze-thaw recovery. If frozen cells were received and not recovered in your lab under the exact, specified conditions (using recommended culture vessel, media, additional supplements, and atmospheric conditions), a live cell replacement is possible at a cost (plus shipping). 3. All of abm's cell biology products are for research use ONLY and NOT for therapeutic/diagnostic applications. abm is not liable for any repercussions arising from the use of its cell biology product(s) in therapeutic/diagnostic application(s). Please contact a technical service representative for more information. 4. abm makes no warranties or representations as to the accuracy of the information on this site. Citations from literature and provided for informational purposes only. abm does not warrant that such information has been shown to be accurate. 5. abm warrants that cell lines shall be viable upon initiation of culture for a period of thirty (30) days after shipment and that they shall meet the specifications on the applicable abm Material Product Information sheet, certificate of analysis, and/or catalog description. Such thirty (30) day period is referred to herein as the "Warranty Period."
Donor History	51, Male, African, Urine
Expression Region	NPHS1, WT1, Resistant to Neomycin
Growth Properties	Adherent, cobblestone-like
Growth Conditions	Use of gelatin coating (TM063) is required for cell adhesion to the culture vessel and optimal proliferation. PriGrow X series medium (TM0208) + + 1% Penicillin/Streptomycin Solution (G255), 37.0?, 5% CO?.?ote: cells display contact inhibition and should be subcultured when 70% confuence to maintain characteristics.?or information regarding cell differentiation, please refer to the Differentiation Protocol PDF under the Documents Tab.
Tissue	Kidney
Notes	1. Visually examine the packaging containers for signs of leakage or breakage. 2. Immediately transfer frozen cells from dry ice packaging to a temperature below -130?, preferably in liquid nitrogen vapor phase storage, until ready for use. To ensure the highest level of viability, thaw the vial and initiate culture as soon as possible upon receipt. If continued storage is desired, the vial should only be stored below -130? or in liquid nitrogen vapor phase. Do not store at -70?, as it will result in loss of viability.
Organism	Human (H. sapiens)
Cryopreservation	Cryopreservation Medium (TM024), or complete growth media with 10% DMSO.

Applications Range	Research Use Only.

Shipping	Ship with dry ice.
Product Format	Frozen
Product Use	This product is intended for laboratory research use only. It is not intended for any animal or human therapeutic use, any human or animal consumption, or any diagnostic use.
Storage	Vapor phase of liquid nitrogen, or below -130?.

Thawing Protocol	1. Thaw cells quickly in a 37? water bath while agitating gently (maximum 2 minutes). The vial cap should be kept above the water level to minimize the risk of contamination. 2. Decontaminate the vial by spraying and wiping the exterior of the vial with 70% ethanol. From this point onwards, all operations should be strictly carried out inside a biological safety cabinet using aseptic conditions. 3. Transfer the cell suspension into a 15ml sterile conical tube containing 5ml of pre-warmed, complete growth media. Centrifuge cells at 125xg for 5-7 minutes. 4. Aspirate the supernatant without disturbing the cell pellet. Re-suspend the cell pellet in the recommended pre-warmed, complete growth media and dispense into a T25 culture flask. 5. Incubate the cells at the recommended conditions.
Subculture Protocol	Volumes given below are for a T75 flask; proportionally increase or decrease the volume as required per culture vessel size. Subculture cells once the culture vessel is 70% confluent. Cells display contact inhibition.?1. Aspirate the culture media, and add 2-3ml of pre-warmed 0.25% Trypsin-EDTA to the culture vessel. 2. Observe the cells under a microscope to confirm detachment (typically within 2-10 minutes). Cells that are difficult to detach can be put in 37?, for several minutes to facilitate detachment. 3. Neutralize Trypsin-EDTA by adding an equal volume of the complete growth media into the culture vessel. 4. Transfer the culture suspension into a sterile centrifuge tube, and centrifuge at 125xg for 5 minutes. The actual centrifuge duration and speed may vary depending on the cell type. 5. Aspirate the supernatant, and re-suspend the pellet with pre-warmed fresh complete growth media. Add appropriate aliquots of the cell suspension to new culture vessels, as desired. 6. Incubate the cells at the recommended conditions.

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SKU	Supplier No.	Size	Your price	Quantity
BHC10902205	T0208	1x10^6 cells / 1.0 ml	-		Add to Quote

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