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RFT1 (NM_052859) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC208160L3V
- LentiORF®
-
Lenti ORF particles, RFT1 (Myc-DDK tagged) - Human RFT1 homolog (S. cerevisiae) (RFT1), 200ul, >10^7 TU/mL
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CNY 8,930.00
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规格
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Specifications
| Product Data | |
| Product Name | RFT1 (NM_052859) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CDG1N |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_052859 |
| ORF Size | 1623 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC208160).
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| OTI Disclaimer | Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. 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_052859.2 |
| RefSeq Size | 5112 bp |
| RefSeq ORF | 1626 bp |
| Locus ID | 91869 |
| Domains | Rft-1 |
| Protein Families | Transmembrane |
| Protein Pathways | N-Glycan biosynthesis |
| MW | 60.3 kDa |
| Gene Summary | This gene encodes an enzyme which catalyzes the translocation of the Man(5)GlcNAc (2)-PP-Dol intermediate from the cytoplasmic to the luminal side of the endoplasmic reticulum membrane in the pathway for the N-glycosylation of proteins. Mutations in this gene are associated with congenital disorder of glycosylation type In.[provided by RefSeq, Dec 2008] |
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