HNRNPF(p.K224R, c.671A>G)Point Mutation in HT-29 Cell Line
Cat.No.:
EDC90377
Species:
Human
Cell Name:
HT-29
Gene:
HNRNPF
Gene ID:
3185
The HNRNPF(p.K224R, c.671A>G)Point Mutation in HT-29 Cell Line is based on the newly developed Bingo™ platform, which utilizes an optimized and upgraded version of the Prime Editing(PE)gene point mutation system-currently the most efficient and safest technology available. This platform enables precise and efficient gene point mutation, resulting in a highly active and stable cell line.
| Cat.No. | EDC90377 |
|---|---|
| Product Name | HNRNPF(p.K224R, c.671A>G)Point Mutation in HT-29 Cell Line |
| Cell Line | HT-29 |
| Gene ID | |
| Cellosaurus ID | CVCL_0320 |
| Mutation Site | p.K224R, c.671A>G |
| Cell Line Synonyms | HT 29, HT29 |
| Gene | HNRNPF |
| Summary |
This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and regulate alternative splicing, polyadenylation, and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has three repeats of quasi-RRM domains that bind to RNAs which have guanosine-rich sequences. This protein is very similar to the family member hnRPH. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
|
| Morphology | Adherent |
| Passage Ratio | 1:2 |
| Complete Culture Medium | McCoy's 5A + 10% FBS |
| Freezing Medium | 95% Complete medium + 5% 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: HT-29 | STR Info (Cell bank) Cell Line: HT-29 | ||
| Allele1 | Allele2 | Allele1 | Allele2 | |
| Amelogenin | X | X | ||
| CSF1PO | 11 | 12 | 11 | 12 |
| D5S818 | 11 | 12 | 11 | 12 |
| D7S820 | 10 | 10 | ||
| D13S317 | 11 | 12 | 11 | 12 |
| D16S539 | 11 | 12 | 11 | 12 |
| TPOX | 8 | 9 | 8 | 9 |
| vWA | 17 | 19 | 17 | 19 |
* 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.
* Research Use Disclaimer: Content is generated from publicly available research data, bioinformatic resources, and computational analyses for research reference only.
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