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GNS (NM_002076) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC204458L4V
- LentiORF®
-
Lenti ORF particles, GNS (mGFP-tagged) - Human glucosamine (N-acetyl)-6-sulfatase (GNS), 200ul, >10^7 TU/mL
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CNY 9,975.00
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规格
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Specifications
| Product Data | |
| Product Name | GNS (NM_002076) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | G6S |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_002076 |
| ORF Size | 1656 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC204458).
|
| 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_002076.2 |
| RefSeq Size | 5144 bp |
| RefSeq ORF | 1659 bp |
| Locus ID | 2799 |
| Domains | Sulfatase |
| Protein Families | Druggable Genome, Transmembrane |
| Protein Pathways | Glycosaminoglycan degradation, Lysosome, Metabolic pathways |
| MW | 62.1 kDa |
| Gene Summary | The product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome. [provided by RefSeq, Jul 2008] |
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