POLDIP3 KO cell line available to order. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 14 bp deletion in exon 1 and 1 bp insertion in exon 1.
Images
Key facts
- Cell type
- HeLa
- Species or organism
- Human
- Tissue
- Cervix
- Form
- Liquid
- Knockout validation
- Sanger Sequencing
- Mutation description
- Knockout achieved by using CRISPR/Cas9, 14 bp deletion in exon 1 and 1 bp insertion in exon 1
Alternative names
46 kDa DNA polymerase delta interaction protein, DNA polymerase delta interacting protein 3, KIAA1649, PDIP3_HUMAN, PDIP46, POLDIP3, Polymerase (DNA-directed), delta interacting protein 3, Polymerase delta interacting protein 46, Polymerase delta-interacting protein 3, RNA-binding protein P46, S6K1 Aly/REF-like target, SKAR
Recommended products
POLDIP3 KO cell line available to order. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 14 bp deletion in exon 1 and 1 bp insertion in exon 1.
Key facts
- Cell type
- HeLa
- Species or organism
- Human
- Tissue
- Cervix
- Form
- Liquid
- Knockout validation
- Sanger Sequencing
- Mutation description
- Knockout achieved by using CRISPR/Cas9, 14 bp deletion in exon 1 and 1 bp insertion in exon 1
- Disease
- Adenocarcinoma
- Concentration
Properties
- Gene name
- POLDIP3
- Gene editing type
- Knockout
- Gene editing method
- CRISPR technology
- Knockout validation
- Sanger Sequencing
Quality control
- STR analysis
- CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
- Biosafety level
- EU: 2 US: 2
- Adherent/suspension
- Adherent
- Gender
- Female
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.
- Culture medium
- DMEM (High Glucose) + 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
P46 also known as heat shock protein 46 (HSP46) is a molecular chaperone within the heat shock protein family. It maintains a mass of approximately 46 kDa and is ubiquitously expressed in various tissues. The protein assists in protein folding and prevents the aggregation of misfolded proteins. It acts in cellular stress responses aiding cells in coping with conditions like heat or oxidative stress. Researchers recognize its important role in maintaining cellular protein homeostasis.
- Biological function summary
Heat shock protein 46 is integral in cellular protection during stress conditions. It participates in forming complexes with other heat shock proteins enhancing its function in assisting proteins during synthesis and repair. This protein acts in maintaining the stability and function of other proteins preserving cellular health under stress. Its involvement in cellular processes signifies its importance in both cellular functioning and stress response mechanisms.
- Pathways
P46 plays a critical role in the heat shock response and protein quality control pathways. It interacts with proteins such as HSP70 and HSP90 which participate in similar pathways ensuring proper folding and stability of newly synthesized proteins. These pathways protect cells from damage during stress connecting p46 to broader physiological responses. Its presence in these pathways emphasizes its significance in cellular recovery and adaptation processes.
- Associated diseases and disorders
P46 connects to neurodegenerative diseases and cancer. In neurodegenerative diseases such as Alzheimer's its function becomes important due to the accumulation of misfolded proteins sharing pathways with proteins like HSP70 which also counteracts protein misfolding. In cancer the overexpression of p46 has been observed linking it to tumor progression where it may stabilize proteins required for tumor growth and survival. These connections highlight how alterations in p46 levels may contribute to disease development and progression.
Product promise
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
2 product images
Sanger Sequencing - Human POLDIP3 (p46) knockout HeLa cell line (ab265843)
Allele-2: 1 bp insertion in exon 1.
Sanger Sequencing - Human POLDIP3 (p46) knockout HeLa cell line (ab265843)
Allele-1: 14 bp deletion in exon 1.
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