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MTH1 (NUDT1) (NM_198948) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC212655L4V
- LentiORF®
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Lenti ORF particles, NUDT1 (mGFP-tagged) - Human nudix (nucleoside diphosphate linked moiety X)-type motif 1 (NUDT1), transcript variant 2A, 200ul, >10^7 TU/mL
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CNY 8,360.00
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| Product Data | |
| Product Name | MTH1 (NUDT1) (NM_198948) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | MTH1 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_198948 |
| ORF Size | 468 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC212655).
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| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_198948.1, NP_945186.1 |
| RefSeq Size | 743 bp |
| RefSeq ORF | 471 bp |
| Locus ID | 4521 |
| Protein Families | Stem cell - Pluripotency |
| MW | 18 kDa |
| Gene Summary | Misincorporation of oxidized nucleoside triphosphates into DNA/RNA during replication and transcription can cause mutations that may result in carcinogenesis or neurodegeneration. The protein encoded by this gene is an enzyme that hydrolyzes oxidized purine nucleoside triphosphates, such as 8-oxo-dGTP, 8-oxo-dATP, 2-hydroxy-dATP, and 2-hydroxy rATP, to monophosphates, thereby preventing misincorporation. The encoded protein is localized mainly in the cytoplasm, with some in the mitochondria, suggesting that it is involved in the sanitization of nucleotide pools both for nuclear and mitochondrial genomes. Several alternatively spliced transcript variants, some of which encode distinct isoforms, have been identified. Additional variants have been observed, but their full-length natures have not been determined. A rare single-nucleotide polymorphism that results in the production of an additional, longer isoform (p26) has been described. [provided by RefSeq, Dec 2018] |
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