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DUSP7 (NM_001947) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC211190L4V
- LentiORF®
-
Lenti ORF particles, DUSP7 (mGFP-tagged)-Human dual specificity phosphatase 7 (DUSP7), 200ul, >10^7 TU/mL
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CNY 10,165.00
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Specifications
| Product Data | |
| Product Name | DUSP7 (NM_001947) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | MKPX; PYST2 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001947 |
| ORF Size | 1104 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC211190).
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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_001947.2, NP_001938.1 |
| RefSeq Size | 3248 bp |
| RefSeq ORF | 1260 bp |
| Locus ID | 1849 |
| Protein Families | Druggable Genome, Phosphatase |
| Protein Pathways | MAPK signaling pathway |
| MW | 40.6 kDa |
| Gene Summary | Dual-specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine-based protein-tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine/threonine residues. DUSP7 belongs to a class of DUSPs, designated MKPs, that dephosphorylate MAPK (mitogen-activated protein kinase) proteins ERK (see MIM 601795), JNK (see MIM 601158), and p38 (see MIM 600289) with specificity distinct from that of individual MKP proteins. MKPs contain a highly conserved C-terminal catalytic domain and an N-terminal Cdc25 (see MIM 116947)-like (CH2) domain. MAPK activation cascades mediate various physiologic processes, including cellular proliferation, apoptosis, differentiation, and stress responses (summary by Patterson et al., 2009 [PubMed 19228121]).[supplied by OMIM, Dec 2009] |
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