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HARS2 (NM_012208) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC204925L3V
- LentiORF®
-
Lenti ORF particles, HARS2 (Myc-DDK tagged) - Human histidyl-tRNA synthetase 2, mitochondrial (putative) (HARS2), nuclear gene encoding mitochondrial protein, 200ul, >10^7 TU/mL
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Specifications
| Product Data | |
| Product Name | HARS2 (NM_012208) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | HARSL; HARSR; HisRS; HO3; PRLTS2 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_012208 |
| ORF Size | 1518 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC204925).
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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_012208.2 |
| RefSeq Size | 2515 bp |
| RefSeq ORF | 1521 bp |
| Locus ID | 23438 |
| Domains | tRNA-synt_2b, HGTP_anticodon |
| Protein Pathways | Aminoacyl-tRNA biosynthesis |
| MW | 56.9 kDa |
| Gene Summary | Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013] |
Documents
| Product Manuals |
| FAQs |
| SDS |
