SLC39A1 Knockout HEK293 Cell Line
Cat.No.:
EDC08027
Species:
Human
Cell Name:
HEK293
Gene:
SLC39A1
Gene ID:
27173
Size:
1×10⁶cells
SLC39A1 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. | EDC08027 |
|---|---|
| Product Name | SLC39A1 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 | SLC39A1 |
| NCBI Gene ID | |
| Gene Synonyms | ZIP1|ZIRTL |
| Summary |
This gene encodes a member of the zinc-iron permease family. The encoded protein is localized to the cell membrane and acts as a zinc uptake transporter. This gene has been linked to prostate cancer, breast cancer, and Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
|
| 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 SLC39A1 function, SLC39A1 Knockout HEK293 Cell Line or SLC39A1 overexpression HEK293 Cell Line?
The choice depends on whether you are studying SLC39A1 (ZIP1)'s role in zinc uptake or its specific contributions distinct from other plasma membrane ZIP family members. The Knockout line is appropriate for asking whether ZIP1 is required for cellular zinc influx — ZIP1 is broadly expressed and contributes to zinc uptake in many cell types. Overexpression is useful for testing transport activity and for studying ZIP1's reported tumor-suppressive role in prostate cancer.
For ZIP1 research, the EDITGENE Knockout in HEK293 is a standard mechanistic platform. ZIP family redundancy is important — ZIP2, ZIP3, ZIP4 expression should be assessed in parallel given functional overlap. Rescue with wild-type or transport-deficient ZIP1 enables structure-function studies.
What are the application scenarios for this model?
Primary applications:
• Zinc uptake kinetics: FluoZin-3 imaging or ⁶⁵Zn uptake assays under various external zinc concentrations.
• Prostate cancer biology: studies of ZIP1 tumor-suppressive function, given reported ZIP1 downregulation in prostate cancer.
• ZIP family redundancy: parallel ZIP2, ZIP3 expression analysis for paralog compensation assessment.
• Inhibitor specificity studies: genetic control for ZIP1-selective compounds.
EDITGENE recommends this model for researchers investigating zinc uptake biology, ZIP family functional specialization, and prostate cancer-relevant zinc biology.
Is this SLC39A1 Knockout HEK293 Cell Line compatible with overexpression rescue experiments?
Yes. ZIP1 rescue experiments require attention to plasma membrane targeting:
• Construct design: use a codon-modified SLC39A1 sequence with a small C-terminal tag (FLAG, HA). ZIP1 has 8 transmembrane domains in the canonical ZIP family architecture.
• Transport-deficient rescue: histidine-rich loop mutations enable mechanistic studies.
• Surface localization validation: confirm plasma membrane localization before functional zinc uptake assays.
• Functional readout: rescue should restore zinc uptake activity measured by zinc-sensitive fluorescent probes.
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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