SLC52A3 Knockout HCT 116 Cell Line

SLC52A3 Knockout HCT 116 Cell Line
Cat.No.:

EDC07753

Species:

Human

Cell Name:

HCT 116

Gene:

SLC52A3

Gene ID:

113278

Size:

1×10⁶cells

SLC52A3 Knockout HCT116 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. EDC07753
Product Name SLC52A3 Knockout HCT116 Cell Line
Species Human
Cell Line HCT 116
Cellosaurus ID CVCL_0291
Cell Line Synonyms HCT-116, HCT.116, HCT_116, HCT116, HCT116wt, HCT-116/P, HCT-116/parental, CoCL2
Gene ID
Gene SLC52A3
Gene Synonyms BVVLS|BVVLS1|C20orf54|RFT2|RFVT3|bA371L19.1|hRFT2
Summary
This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]
Associated Diseases Colorectal Carcinoma
Digestion Time 3 min
Morphology Adherent
Passage Ratio 1:8~1:10
Complete Culture Medium mcCoy5A+10% FBS
Freezing Medium 90% FBS/complete culture medium+10% DMSO
* 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: HCT 116
STR Info (Cell bank)
Cell Line: HCT 116
Allele1Allele2Allele3Allele4Allele1Allele2Allele3Allele4
Amelogenin X X
CSF1PO 7 10 7 9 10 11
D2S1338 16 16
D3S1358 12 17 18 19 12 18 19
D5S818 10 11 10 11
D7S820 11 12 11 12
D8S1179 10 12 14 15 10 12 14 15
D13S317 10 12 10 12
D16S539 11 13 11 12 13 14
D18S51 16 17 16 17
D19S433 12 13 12
D21S11 29 30 29 30
FGA 18 23 18 23
Penta D 9 13 9 13
Penta E 12 13 14 12 13 14
TH01 8 9 8 9
TPOX 8 8
vWA 17 21 22 23 17 21 22 23
D6S1043 13
D12S391 17 21 22
D2S441 11 12
* 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 SLC52A3 (RFVT3)'s role in riboflavin (vitamin B2) transport or modeling Brown-Vialetto-Van Laere syndrome. The Knockout line is the standard tool for asking whether RFVT3 is required for cellular riboflavin uptake — RFVT3 is the principal apical riboflavin transporter in intestine. Overexpression is useful for transport kinetics studies and for testing therapeutic riboflavin supplementation strategies. For riboflavin biology research, the EDITGENE SLC52A3 Knockout in HCT 116 is particularly relevant for intestinal riboflavin absorption studies — HCT 116 has an intestinal epithelial origin. SLC52A3 mutations cause Brown-Vialetto-Van Laere syndrome type 2 (motor neuron disease responsive to riboflavin supplementation) — disease variant rescue enables genotype-function studies. Rescue with wild-type or transport-deficient RFVT3 is the standard specificity control.
Primary applications: • Riboflavin uptake: ³H-riboflavin uptake assays to quantify RFVT3-dependent cellular vitamin B2 acquisition. • Disease modeling: rescue with Brown-Vialetto-Van Laere syndrome type 2-associated SLC52A3 mutations for genotype-function studies. • Therapeutic riboflavin response: testing whether high-dose riboflavin can rescue functions in cells expressing specific BVVL mutants. • RFVT paralog studies: SLC52A1 (RFVT1) and SLC52A2 (RFVT2) expression analysis to interpret intestinal riboflavin transport network. EDITGENE recommends this model for researchers investigating riboflavin biology, Brown-Vialetto-Van Laere syndrome, and intestinal vitamin B2 absorption.
Yes. RFVT3 rescue experiments are well-established for riboflavin biology research: • Construct design: use a codon-modified SLC52A3 sequence with a small C-terminal tag (FLAG, HA). The 11 transmembrane SLC52 architecture must be preserved. • BVVL mutation rescue: introduction of patient-derived SLC52A3 mutations enables disease genotype-function correlation in a controlled background. • Therapeutic riboflavin testing: rescue with disease variants combined with high-dose riboflavin treatment models the clinical therapeutic response. • Functional readout: rescue should restore ³H-riboflavin uptake activity. HCT 116 transduces efficiently with lentivirus and is appropriate for intestinal riboflavin absorption studies.
* Research Use Disclaimer: Content is generated from publicly available research data, bioinformatic resources, and computational analyses for research reference only.

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