SLC39A1 Knockout HEK293 Cell Line

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.
LociSTR Info (Sample Cell)
Sample Cell Line: HEK293
STR Info (Cell bank)
Cell Line: HEK293
Allele1Allele2Allele1Allele2
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.

FAQ

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.
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.
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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