SLC30A1 Knockout HEK293 Cell Line

SLC30A1 Knockout HEK293 Cell Line
Cat.No.:

EDC08069

Species:

Human

Cell Name:

HEK293

Gene:

SLC30A1

Gene ID:

7779

Size:

1×10⁶cells

SLC30A1 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. EDC08069
Product Name SLC30A1 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 SLC30A1
NCBI Gene ID
Gene Synonyms ZNT1|ZRC1
Summary
Predicted to enable calcium channel inhibitor activity and zinc:proton antiporter activity. Involved in defense response to bacterium; intracellular zinc ion homeostasis; and zinc ion import into organelle. Located in several cellular components, including Golgi apparatus; basolateral plasma membrane; and nuclear membrane. [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.
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 SLC30A1 (ZnT1)'s role as the principal plasma membrane zinc efflux transporter or its functions in cellular zinc homeostasis. The Knockout line is the standard tool for asking whether ZnT1 is required for cellular zinc export — ZnT1 is the major zinc extrusion transporter in most cell types and is essential for preventing intracellular zinc overload. Overexpression is useful for testing whether elevated ZnT1 enhances zinc efflux or for studying cancer-associated ZnT1 regulation. For zinc homeostasis research, the EDITGENE SLC30A1 Knockout in HEK293 enables study of cellular zinc efflux and tolerance to zinc challenge. Note that complete ZnT1 loss may sensitize cells to zinc toxicity — characterize zinc tolerance phenotypes before extended use. Rescue with wild-type or transport-deficient ZnT1 enables structure-function studies.
Primary applications: • Cellular zinc efflux: zinc-sensitive fluorescent probe (FluoZin-3) imaging following zinc challenge to quantify ZnT1 export activity. • Zinc tolerance assays: cell viability and growth assays under varied extracellular zinc concentrations to characterize zinc sensitivity in the absence of ZnT1. • ZnT family compensation: ZnT family member expression profiling to assess compensatory upregulation in ZnT1-null cells. • Cancer biology: zinc handling in cancer contexts where altered ZnT1 expression has been associated with tumor progression. EDITGENE recommends this model for researchers investigating cellular zinc efflux biology and zinc homeostasis under physiological and challenge conditions.
Yes. ZnT1 rescue experiments require attention to plasma membrane targeting: • Construct design: use a codon-modified SLC30A1 sequence with a small C-terminal tag (FLAG, HA). The 6 transmembrane ZnT family architecture must be preserved. • Transport-deficient rescue: histidine-rich loop mutations or transmembrane zinc-binding site mutations enable structure-function studies. • Surface localization validation: confirm plasma membrane localization by cell surface staining before zinc efflux assays. • Functional readout: rescue should restore cellular zinc efflux and zinc tolerance under challenge conditions. 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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