Human IFI16 knockout A549 cell line
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IFI16 KO cell line available to order. KO validated by. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon 2 and 1 bp insertion in exon 2.
View Alternative Names
Gamma interferon inducible protein 16, Gamma-interferon-inducible protein Ifi16, IF16_HUMAN, IFNGIP1, Ifi-204, Interferon gamma induced protein IFI 16, Interferon gamma inducible protein 16, Interferon-inducible myeloid differentiation transcriptional activator, PYHIN2, interferon activated gene 204, p204
- Sanger seq
Unknown
Sanger Sequencing - Human IFI16 knockout A549 cell line (AB267143)
Allele-2 : 1 bp insertion in exon 2.
- Cell Culture
Unknown
Cell Culture - Human IFI16 knockout A549 cell line (AB267143)
Representative images of IFI16 knockout A549 cells, low and high confluency examples (top left and right respectively) and wild-type A549 cells, low and high confluency (bottom left and right respectively) showing typical adherent, epithelial-like morphology. Images were captured at 10X magnification using an EVOS M5000 microscope.
- Sanger seq
Unknown
Sanger Sequencing - Human IFI16 knockout A549 cell line (AB267143)
Allele-1 : 1 bp deletion in exon2
Product details
Recommended control: Human wild-type A549 cell line (ab255450). Please note a wild-type cell line is not automatically included with a knockout cell line order, if required please add recommended wild-type cell line at no additional cost using the code WILDTYPE-TMTK1.
We will provide viable cells that proliferate on revival.
This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.
What's included?
Properties and storage information
Gene name
Gene editing type
Gene editing method
Knockout validation
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Handling procedures
Initial handling guidelines
Upon arrival, the vial should be stored in liquid nitrogen vapor phase and not at -80°C. Storage at -80°C may result in loss of viability.
1. Thaw the vial in 37°C water bath for approximately 1-2 minutes.
2. Transfer the cell suspension (0.8 mL) to a 15 mL/50 mL conical sterile polypropylene centrifuge tube containing 8.4 mL pre-warmed culture medium, wash vial with an additional 0.8 mL culture medium (total volume 10 mL) to collect remaining cells, and centrifuge at 201 x g (rcf) for 5 minutes at room temperature. 10 mL represents minimum recommended dilution. 20 mL represents maximum recommended dilution.
3. Resuspend the cell pellet in 5 mL pre-warmed culture medium and count using a haemocytometer or alternative cell counting method seed all remaining cells into a T25.
4. Incubate the culture at 37°C incubator with 5% CO2. Check the culture one day after revival and continue to check until 80% confluent. Media change can be given if needed.
5. Once confluent passage into an appropriate flask at a density of 2x104 cells/cm2. Seeding density is given as a guide only and should be scaled to align with individual lab schedules. Cultures should be monitored daily.
Subculture guidelines
- All seeding densities should be based on cell counts gained by established methods.
- A guide seeding density of 2x104 cells/cm2 is recommended.
- Cells should be passaged when they have achieved 80-90% confluence.
- Do not allow the cell density to exceed 7x104 cells/cm2.
Culture medium
F-12K + 10% FBS
Cryopreservation medium
Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
IFI16 protein participates in the innate immune response by recognizing viral and bacterial double-stranded DNA. It forms part of a signaling complex that activates pathogen recognition receptors and induces the production of type I interferons. IFI16 can interact with various DNA sensors and is known for its ability to bind DNA directly providing a defense mechanism against infection. The protein also plays a role in the regulation of transcription which contributes to cell growth and differentiation.
Pathways
IFI16 protein has significant roles in the cGAS-STING and BRCA1 pathways. It interacts with cGAS to regulate the production of cyclic GMP-AMP activating STING and promoting antiviral responses. Additionally IFI16 aligns with BRCA1 dysfunction impacting DNA repair processes. This interaction underlines its involvement in maintaining genomic integrity and modulating the immune responses along with cGAS STING and BRCA1 proteins which are critical in these pathways.
Quality control
STR analysis
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
Biosafety level
EU: 1 US: 1
Adherent/suspension
Adherent
Gender
Male
Target data
Complementary Products
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com