PARP12 KO cell line available to order. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 3.
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Key facts
- Cell type
- A549
- Species or organism
- Human
- Tissue
- Lung
- Form
- Liquid
- Knockout validation
- Sanger Sequencing
- Mutation description
- Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 3
Alternative names
9930021O16, AA409132, AA536654, FLJ22693, HGNC:21919, MST109, MSTP109, OTTMUSP00000026964, PAR12_HUMAN, Poly (ADP ribose) polymerase family member 12, Poly [ADP-ribose] polymerase 12, ZC3HDC1, Zinc finger CCCH domain-containing protein 1, Zinc finger CCCH type domain containing 1
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PARP12 KO cell line available to order. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 3.
Key facts
- Cell type
- A549
- Species or organism
- Human
- Tissue
- Lung
- Form
- Liquid
- Knockout validation
- Sanger Sequencing
- Mutation description
- Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 3
- Disease
- Carcinoma
- Concentration
Properties
- Gene name
- PARP12
- Gene editing type
- Knockout
- Gene editing method
- CRISPR technology
- Knockout validation
- Sanger Sequencing
- Zygosity
- Homozygous
Quality control
- STR analysis
- CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
- Biosafety level
- EU: 1 US: 1
- Adherent/suspension
- Adherent
- Gender
- Male
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.
Storage
- Shipped at conditions
- Dry Ice
- Appropriate short-term storage conditions
- -196°C
- Appropriate long-term storage conditions
- -196°C
Notes
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.
Supplementary info
- This supplementary information is collated from multiple sources and compiled automatically.
- Activity summary
PARP12 or poly (ADP-ribose) polymerase family member 12 plays a role in post-translational modifications within cells. It functions in mono-ADP-ribosylation a process which affects various proteins' activities by adding ADP-ribose to them. This protein has a calculated mass of approximately 78 kDa. It expresses in various tissues including the liver and immune cells contributing to cellular responses and defense mechanisms.
- Biological function summary
Mono-ADP-ribosylation modulates cellular activities affecting processes like viral response and inflammation. PARP12 is part of the broader PARP protein family known for roles in DNA repair and cellular stress responses though PARP12 focuses more on antiviral and stress-related pathways. It does not typically engage in large multi-protein complexes but interacts closely with other molecules within its signaling network to execute its functions.
- Pathways
Interactions within antiviral defense mechanisms and inflammation regulation highlight the role of PARP12. It contributes to pathways like the Interferon signaling response enhancing the cell's ability to combat viral infections. Interactions with other PARP family members such as PARP1 and PARP5 further integrate its function into broader cellular immune pathways ensuring a coordinated response to external stressors.
- Associated diseases and disorders
PARP12's involvement predominantly impacts viral infections and inflammatory conditions. It relates to viral response pathways such as those engaged in HIV replication repression highlighting its significance in infectious disease contexts. Furthermore PARP12 connects with proteins like PARP13 in modulating processes involved in immune responses offering insights into managing inflammation-related diseases.
Product promise
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Terms & Conditions.
1 product image
Sanger Sequencing - Human PARP12 knockout A549 cell line (ab267220)
Homozygous: 1 bp insertion in exon3
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