CCDC82 Knockout HEK293 Cell Line
Cat.No.:
EDC90431
Species:
Human
Cell Name:
HEK293
Gene:
CCDC82
Gene ID:
79780
Size:
1×10⁶cells
CCDC82 Knockout Cell Line (HEK293) is an exclusive upgraded CRISPR/Cas9 system-mediated gene knockout cell, with the advantages of Optimized Strategy Design, Efficient Cell Transfection, High-Performance Cas9 Protein and Hassle-Free Cell Selection.
| Cat.No. | EDC90431 |
|---|---|
| Product Name | CCDC82 Knockout Cell Line (HEK293) |
| Cell Line | HEK293 |
| Cellosaurus ID | CVCL_0045 |
| Cell Line Synonyms | Hek293, HEK-293, HEK/293, (HEK)293, HEK 293, HEK,293, 293, 293 HEK, 293 Ad5, Graham 293, Graham-293, Human Embryonic Kidney 293 |
| Gene | |
| NCBI Gene ID | |
| Gene Synonyms | HSPC048 |
| Summary |
Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
|
| Associated Diseases | Non-tumor |
| Morphology | Adherent |
| Passage Ratio | 1/5,2days |
| Complete Culture Medium | DMEM + 10% FBS |
| Freezing Medium | 95% Complete culture medium+ 5% DMSO |
| QC | Indels validated by Sanger sequencing; sterility confirmed via microbial testing. |
* For research use only. Not intended for use in humans or animals, including clinical, therapeutic, or diagnostic purposes.
| Loci | STR Info (Sample Cell) Sample Cell Line: HEK293 | STR Info (Cell bank) Cell Line: HEK293 | ||
| Allele1 | Allele2 | Allele1 | Allele2 | |
| Amelogenin | X | X | ||
| CSF1P0 | 12 | 11 | 12 | |
| D2S1338 | 19 | 19 | ||
| D3S1358 | 15 | 17 | 15 | 17 |
| D5S818 | 8 | 8 | 9 | |
| D7S820 | 11 | 12 | 11 | 12 |
| D8S1179 | 12 | 14 | 12 | 14 |
| D13S317 | 12 | 14 | 12 | 14 |
| D16S539 | 9 | 13 | 9 | 13 |
| D18S51 | 17 | 18 | 17 | 18 |
| D19S433 | 15 | 18 | 15 | 18 |
| D21S11 | 28 | 30.2 | 28 | 30.2 |
| FGA | 23 | 23 | ||
| Penta D | 9 | 10 | 9 | 10 |
| Penta E | 7 | 15 | 7 | 15 |
| TH01 | 7 | 9.3 | 7 | 9.3 |
| TPOX | 11 | 11 | ||
| vWA | 16 | 19 | 16 | 19 |
| D6S1043 | 11 | 11 | ||
| D12S391 | 19 | 21 | 11 | 15 |
| D2S441 | 11 | 15 | 11 | 15 |
* STR authentication data of this cell line matches with that of cell lines sourced from ATCC, DSMZ, JCRB, and RIKEN databases.
Conclusion: The STR identification of this cell is correct.
Conclusion: The STR identification of this cell is correct.
FAQ
Which is better for studying CCDC82 function, CCDC82 Knockout HEK293 Cell Line or CCDC82 overexpression HEK293 Cell Line?
The choice depends on the experimental question. CCDC82 (coiled-coil domain containing 82) is an emerging less-characterized gene with limited published functional data. The Knockout line is appropriate for asking whether CCDC82 is required for predicted activities — CCDC82 is a coiled-coil domain-containing protein with no established specific function in the current literature; CCDC family members have diverse roles including ciliary function, mitosis, and signaling. Overexpression is useful for studying CCDC82 in heterologous expression contexts.
For discovery research, the EDITGENE CCDC82 Knockout in HEK293 provides a clean genetic background for characterizing emerging CCDC82 biology. Rescue with wild-type CCDC82 is the standard specificity control. The knockout is valuable for CCDC family discovery research, interactome analysis, and emerging functional characterization of less-studied genes.
What are the application scenarios for this model?
Primary applications:
• Discovery proteomics: interactome analysis in CCDC82-null versus rescued cells to identify candidate binding partners.
• Phenotypic discovery: parallel wild-type rescue during phenotypic characterization distinguishes CCDC82-dependent phenotypes.
• Coiled-coil family comparative studies: comparison with other CCDC family members for emerging functional characterization.
• CCDC82 substrate identification: discovery-oriented studies in CCDC82-null versus rescued cells.
EDITGENE recommends this model for researchers investigating less-characterized CCDC family biology and CCDC82 function discovery.
Is this CCDC82 Knockout HEK293 Cell Line compatible with overexpression rescue experiments?
Yes. CCDC82 rescue experiments require attention to less-characterized protein architecture:
• Construct design: use a codon-modified CCDC82 sequence with a small C-terminal tag (FLAG, HA). CCDC82 has coiled-coil domain — preserve protein integrity.
• Discovery-oriented rescue: parallel wild-type rescue during phenotypic characterization distinguishes CCDC82-dependent phenotypes.
• Functional readout: rescue should restore CCDC82-dependent phenotypes identified during knockout characterization.
HEK293 transduces efficiently with lentivirus and supports stable rescue line generation.
* Research Use Disclaimer: Content is generated from publicly available research data, bioinformatic resources, and computational analyses for research reference only.
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