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PEX7 (NM_000288) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC202432L2V
- LentiORF®
-
Lenti ORF particles, PEX7 (mGFP-tagged) - Human peroxisomal biogenesis factor 7 (PEX7), 200ul, >10^7 TU/mL
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CNY 9,120.00
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规格
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Specifications
| Product Data | |
| Product Name | PEX7 (NM_000288) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | PBD9B; PTS2R; RCDP1; RD |
| Vector | pLenti-C-mGFP |
| ACCN | NM_000288 |
| ORF Size | 969 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC202432).
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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_000288.1 |
| RefSeq Size | 1451 bp |
| RefSeq ORF | 972 bp |
| Locus ID | 5191 |
| Domains | WD40 |
| Protein Families | Druggable Genome |
| MW | 35.7 kDa |
| Gene Summary | This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq, Oct 2008] |
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