IGFLR1 Knockout HEK293 Cell Line

IGFLR1 Knockout HEK293 Cell Line
Cat.No.:

EDC90018

Species:

Human

Cell Name:

HEK293

Gene:

IGFLR1

Gene ID:

79713

Size:

1×10⁶cells

IGFLR1 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. EDC90018
Product Name IGFLR1 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 IGFLR1
NCBI Gene ID
Gene Synonyms TMEM149
Summary
Located in nucleoplasm and plasma 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 the experimental question. IGFLR1 (IGF-like family receptor 1, TMEM149) is an emerging T cell costimulatory molecule with limited functional characterization. The Knockout line is appropriate for asking whether IGFLR1 is required for predicted activities — IGFLR1 has been characterized as a costimulatory molecule expressed on activated T cells and Treg cells, with TNFR-family-like structural features and emerging roles in T cell activation and tumor immunology. Overexpression is useful for studying IGFLR1 in heterologous expression contexts. For T cell costimulation research, the EDITGENE IGFLR1 Knockout in HEK293 provides a clean genetic background for IGFLR1 structure-function studies. Rescue with wild-type IGFLR1 is the standard specificity control. The knockout is valuable for studying IGFLR1-mediated T cell costimulation and emerging IGFLR1-targeted immunotherapy approaches — IGFLR1 is a less-characterized but emerging cancer immunotherapy target distinct from canonical checkpoint molecules.
Primary applications: • T cell costimulation studies: in heterologous T cell-relevant contexts, characterization of IGFLR1-mediated T cell activation. • Treg biology: in heterologous Treg-relevant contexts, IGFLR1's role in regulatory T cell function. • Surface expression characterization: IGFLR1 plasma membrane expression and ligand identification studies. • Discovery proteomics: interactome analysis in IGFLR1-null versus rescued cells. EDITGENE recommends this model for researchers investigating IGFLR1 biology and emerging T cell costimulation pathways distinct from canonical checkpoint molecules.
Yes. IGFLR1 rescue experiments require attention to membrane topology: • Construct design: use a codon-modified IGFLR1 sequence with a small intracellular C-terminal tag (FLAG, HA). IGFLR1 has the TNFR-family-like architecture (extracellular ligand-binding region, single transmembrane span, intracellular tail) — preserve all elements. • Surface localization validation: confirm plasma membrane localization by cell surface staining before functional assays. • Discovery-oriented rescue: parallel wild-type rescue during phenotypic characterization distinguishes IGFLR1-dependent phenotypes. • Functional readout: rescue should restore 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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