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- 爱必梦(abm)
- T0687
- 2025年07月15日
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- 保存条件：
详询
- 库存：
99
- 供应商：
广州市左克生物
- 规格：
1x10⁶ cells / 1.0 ml
| Cat. No. | T0687 |
| Name | Immortalized Canine Bone Marrow Mesenchymal Stromal Cells (DS1) |
| Description |
Mesenchymal stromal cells are observed to have immunosuppressive effects on lymphocytes. The Immortalized Canine Bone Marrow Mesenchymal Stromal Cells (DS1) cells were generated from mononuclear cells derived from canine bone marrow. The cells were immortalized via transduction of a retrovirus containing the human papilloma virus E6/E7 genes. Phenotypic characterization of the Immortalized Canine Bone Marrow Mesenchymal Stromal Cells (DS1) cells via RT-PCR found that the cell line was weakly positive for CD10, CD29, CD106, moderately positive for CD73 and CD105, and strongly positive for CD90. The Immortalized Canine Bone Marrow Mesenchymal Stromal Cells (DS1) cells are applicable studies to investigate their immunosuppressive effects, especially in inflammatory and immune disease models. |
| Organism | Dog (Canine) |
| Tissue | Bone Marrow |
| Growth Properties | Adherent, polygonal |
| Cell Type | Immortalized Cells |
| Storage Condition | Vapor phase of liquid nitrogen, or below -130°C. |
| Shipping Conditions | Ship with dry ice. |
| Product Format | Frozen |
| Intended 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. |
| BioSafety | II |
| Certificate of Analysis | For batch-specific test results, refer to the applicable certificate of analysis that can be found at www.abmgood.com. |
| Growth Conditions | Use of PriCoat™ T25 Flasks (G299) or Applied Cell Extracellular Matrix (G422) is required for cell adhesion to the culture vessels. PriGrow III (TM003) + 2 mM L-glutamine (G275) + 10% FBS + 1% Penicillin/Streptomycin Solution (G255), 37.0°C, 5% CO₂ |
| Unpacking and Storage Instructions |
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°C, 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°C or in liquid nitrogen vapor phase. Do not store at -70°C, as it will result in loss of viability. |
| Thawing Protocol |
1. Thaw cells quickly in a 37°C 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 80% confluent. 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°C, 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. |
| Cryopreservation | Cryopreservation Medium (TM024), or complete growth media with 10% DMSO. |
| Seeding Density (cells/cm2) | 20,000 |
| Population Doubling Time (h) | 15 - 20 |
| Immortalization Method | Transduction with retrovirus containing the HPV E6/E7 genes |
| Expression | Weakly positive for CD10, CD29, CD106, moderately positive for CD73 and CD105, and strongly positive for CD90 |
| Material Citation | If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. T0687. |
| Warranty | 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”. |
| Disclaimer |
1. All test parameters provided in the CoA are conducted using abm's standardized culture system and 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 μg, Cat.# C207, $450.00) or cell lysate (100 μg, 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 order placement. 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. 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 or any other non-RUO application(s). 4. abm makes no warranties or representations as to the accuracy of the information on this site. Citations from literature are 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".
|
| Depositor | Fred Hutchinson Cancer Research Center |
| Application | Research Use Only. |
| Material Citation | If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. T0687 |
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文献和实验「铲屎官」注意了！剑桥大学揭示这些基因的改变或让猫猫狗狗成为
的参考意义。图片来源：Cell Reports主要研究内容犬细胞中 caspase-1/-4 融合蛋白的活性相对较低相比于人类和小鼠，猫犬等肉食动物的炎症小体效应器即 caspase 家族蛋白存在较大差异。其中，caspase-1/-4 融合蛋白是肉食动物独有的 caspase 蛋白，能够切割消皮素 D（Gasdermin D），但对 IL-1β 和 IL-18 的作用较弱。首先，为了观察肉食动物中炎症小体的作用，研究者使用鼠伤寒沙门菌作为炎症小体的刺激因素，分别感染小鼠中永生化的骨髓来源的巨噬
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