SLC17A2 Knockout Huh-7 Cell Line
Cat.No.:
EDC08359
Species:
Human
Cell Name:
Huh-7
Gene:
SLC17A2
Gene ID:
10246
Size:
1×10⁶cells
SLC17A2 Knockout Huh-7 Cell Line is an exclusive upgraded CRISPR/Cas9 system-mediated gene knockout cell, with the advantages of Optimized Strategy Design, Efficient Cell Transfection, High-Performotion Cas9 Protein and Hassle-Free Cell Selection.
| Cat.No. | EDC08359 |
|---|---|
| Product Name | SLC17A2 Knockout Huh-7 Cell Line |
| Species | Human |
| Cell Line | Huh-7 |
| Cellosaurus ID | CVCL_0336 |
| Gene ID | |
| Cell Line Synonyms | HuH-7, HUH-7, HuH7, Huh7, HUH7, HUH7.0, JTC-39, Japanese Tissue Culture-39 |
| Gene | SLC17A2 |
| Summary |
Predicted to enable urate transmembrane transporter activity. Predicted to be involved in phosphate-containing compound metabolic process and sodium ion transport. Predicted to be located in plasma membrane. Predicted to be active in apical plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
|
| Digestion Time | 2 min |
| Morphology | Adherent |
| Passage Ratio | 1:3 |
| Complete Culture Medium | DMEM + 10% FBS |
| Freezing Medium | 70% Complete medium + 20% FBS + 10% DMSO |
* 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: Huh-7 | STR Info (Cell bank) Cell Line: Huh-7 | ||
| Allele1 | Allele2 | Allele1 | Allele2 | |
| Amelogenin | X | X | ||
| CSF1P0 | 11 | 11 | ||
| D2S1338 | 19 | 19 | ||
| D3S1358 | 15 | 15 | ||
| D5S818 | 12 | 12 | ||
| D7S820 | 11 | 11 | ||
| D8S1179 | 14 | 14 | 15 | |
| D13S317 | 10 | 11 | 10 | 11 |
| D16S539 | 10 | 10 | ||
| D18S51 | 15 | 15 | ||
| D19S433 | 13 | 14 | 13 | 14 |
| D21S11 | 30 | 30 | ||
| FGA | 22 | 23 | 22 | 23 |
| Penta D | 12 | 12 | ||
| Penta E | 11 | 11 | ||
| TH01 | 7 | 7 | ||
| TPOX | 8 | 11 | 8 | 11 |
| vWA | 16 | 18 | 16 | 18 |
| D6S1043 | 13 | 15 | 13 | 15 |
| D12S391 | 20 | 21 | 20 | 21 |
| D2S441 | 12 | 14 | 12 | 14 |
* 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 SLC17A2 function, SLC17A2 Knockout Huh-7 Cell Line or SLC17A2 overexpression Huh-7 Cell Line?
The choice depends on whether you are studying SLC17A2 (sodium-dependent phosphate transporter)'s role in phosphate handling or its characterization as one of the more poorly-defined SLC17 family members. The Knockout line is appropriate for asking whether SLC17A2 is required for predicted phosphate transport activities, with the caveat that SLC17A2 is less well characterized than other SLC17 family members. Overexpression is useful for substrate identification and transport activity characterization.
For SLC17 family research, the EDITGENE SLC17A2 Knockout in Huh-7 enables characterization of this transporter's substrate scope and tissue-relevant functions in hepatic context. Rescue with wild-type SLC17A2 enables initial functional characterization.
What are the application scenarios for this model?
Primary applications:
• Sodium-phosphate transport: ³²P-orthophosphate uptake assays under varied sodium conditions to characterize SLC17A2 activity.
• Substrate scope characterization: testing organic anion substrates given SLC17 family's vesicular organic anion transporter activities.
• Subcellular localization studies: imaging-based analysis of exogenous SLC17A2 trafficking in rescue cell lines.
• Family comparative studies: parallel analysis with other SLC17 family members for functional specialization.
EDITGENE recommends this model for researchers investigating SLC17 family transporter biology and hepatic phosphate/organic anion handling.
Is this SLC17A2 Knockout Huh-7 Cell Line compatible with overexpression rescue experiments?
Yes, and rescue experiments are particularly important for substrate characterization:
• Construct design: use a codon-modified SLC17A2 sequence with a small C-terminal tag (FLAG, HA). The 12-transmembrane SLC17 architecture should be preserved.
• Discovery-oriented rescue: parallel rescue with wild-type construct during phenotypic characterization helps distinguish SLC17A2-dependent phenotypes.
• Localization validation: confirm subcellular localization by imaging given limited prior characterization.
• Functional readout: rescue should restore phenotypes identified during knockout characterization; substrate-specific transport assays test predicted activities.
Huh-7 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.