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PEX19 (NM_001193644) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC231120L3V
- LentiORF®
-
Lenti ORF particles, PEX19 (Myc-DDK tagged) - Human peroxisomal biogenesis factor 19 (PEX19), transcript variant 4, 200ul, >10^7 TU/mL
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CNY 8,170.00
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Specifications
| Product Data | |
| Product Name | PEX19 (NM_001193644) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | D1S2223E; HK33; PBD12A; PMP1; PMPI; PXF; PXMP1 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001193644 |
| ORF Size | 837 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC231120).
|
| 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_001193644.1, NP_001180573.1 |
| RefSeq ORF | 840 bp |
| Locus ID | 5824 |
| Protein Families | Druggable Genome |
| MW | 31.2 kDa |
| Gene Summary | This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some 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 are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010] |
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