SP100 Stable Knockout HEp-2 Cell Line
Cat. No.
T6135
Unit
1x10⁶ cells / 1 ml
Price
Inquiry
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Sale of this item is subjected to the completion of a Material Transfer Agreement (MTA) by the purchasing institution.
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Specifications
| Description |
Nuclear domain 10 (ND10) bodies are membrane-less cellular components found in the nucleus that affect transcription and are implicated in some immune functions. ND10 bodies are able to detect and respond to viruses that infect cells although many viruses have evolved to degrade or evade these ND 10 bodies. HSV-1 virus has the ability to degrade both the SP100 and PML ND10 bodies. Other viruses even have the ability to repurpose ND10 bodies to use in their replication. The SP100 Stable Knockout HEp-2 Cell Line has been previously used in research to better understand the role of ND10 bodies (SP100) host defences against viral infection. The cell line is ideal for virology research and studies pertaining to innate immune defences at the cellular level. |
| Cat. No. | T6135 |
| Name | SP100 Stable Knockout HEp-2 Cell Line |
| Unit | 1x10⁶ cells / 1 ml |
| Price | Inquiry |
| Category | CRISPR Stable Knockout Cell Line |
| Cell Type | CRISPR Knockout Cell Line |
| Organism | Human (H. sapiens) |
| Tissue | Cervix |
| Donor History | Female, 50, African American, Human papillomavirus-related endocervical adenocarcinoma |
| Cell Morphology | Epithelial |
| Growth Properties | Adherent, epithelial |
| 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) +5% FBS + 1% Penicillin/Streptomycin Solution (G255), 37.0°C, 5% CO₂. Selection with 2 µg/ml Puromycin (G264) |
| 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. |
| Application | Research Use Only. |
| Storage Condition | Vapor phase of liquid nitrogen, or below -130°C. |
| BioSafety | II |
| Disclaimer |
1. Sale of this item is subjected to the completion of a Material Transfer Agreement (MTA) by the purchasing individual/institution for each cell line. If you have any questions regarding this, please contact us at licensing@abmgood.com. 2. 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. 3. 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. 4. 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). 5. 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. 6. 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 | University of Chicago |
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