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PTRH2 (NM_016077) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC201462L1V
- LentiORF®
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Lenti ORF particles, PTRH2 (Myc-DDK tagged) - Human peptidyl-tRNA hydrolase 2 (PTRH2), nuclear gene encoding mitochondrial protein, 200ul, >10^7 TU/mL
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CNY 7,410.00
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Specifications
| Product Data | |
| Product Name | PTRH2 (NM_016077) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BIT1; CFAP37; CGI-147; IMNEPD; PTH; PTH 2; PTH2 |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_016077 |
| ORF Size | 537 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC201462).
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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_016077.3 |
| RefSeq Size | 804 bp |
| RefSeq ORF | 540 bp |
| Locus ID | 51651 |
| Protein Families | Transmembrane |
| MW | 19.2 kDa |
| Gene Summary | The protein encoded by this gene is a mitochondrial protein with two putative domains, an N-terminal mitochondrial localization sequence, and a UPF0099 domain. In vitro assays suggest that this protein possesses peptidyl-tRNA hydrolase activity, to release the peptidyl moiety from tRNA, thereby preventing the accumulation of dissociated peptidyl-tRNA that could reduce the efficiency of translation. This protein also plays a role regulating cell survival and death. It promotes survival as part of an integrin-signaling pathway for cells attached to the extracellular matrix (ECM), but also promotes apoptosis in cells that have lost their attachment to the ECM, a process called anoikos. After loss of cell attachment to the ECM, this protein is phosphorylated, is released from the mitochondria into the cytosol, and promotes caspase-independent apoptosis through interactions with transcriptional regulators. This gene has been implicated in the development and progression of tumors, and mutations in this gene have been associated with an infantile multisystem neurologic, endocrine, and pancreatic disease (INMEPD) characterized by intellectual disability, postnatal microcephaly, progressive cerebellar atrophy, hearing impairment, polyneuropathy, failure to thrive, and organ fibrosis with exocrine pancreas insufficiency (PMID: 25574476). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015] |
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