GCS1 (MOGS) (NM_006302) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206689L1V

  • LentiORF®

Lenti ORF particles, MOGS (Myc-DDK tagged) - Human mannosyl-oligosaccharide glucosidase (MOGS), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro


Biosafety Sheet

USD 1,316.00

2 Weeks*

Size
    • 200 ul

Product Images

Frequently bought together (2)
Lenti ORF control particles of pLenti-C-Myc-DDK, >10^7 TU/mL, 0.5 mL
    • 500 ul

USD 365.00


One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
    • 96 reactions

USD 671.00

Other products for "GCS1"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol GCS1
Synonyms CDG2B; CWH41; DER7; GCS1
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_006302
ORF Size 2511 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC206689).
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_006302.2
RefSeq Size 2910 bp
RefSeq ORF 2514 bp
Locus ID 7841
UniProt ID Q13724
Cytogenetics 2p13.1
Domains Glyco_hydro_63
Protein Families Druggable Genome, Transmembrane
Protein Pathways Metabolic pathways, N-Glycan biosynthesis
MW 91.9 kDa
Gene Summary This gene encodes the first enzyme in the N-linked oligosaccharide processing pathway. The enzyme cleaves the distal alpha-1,2-linked glucose residue from the Glc(3)-Man(9)-GlcNAc(2) oligosaccharide precursor. This protein is located in the lumen of the endoplasmic reticulum. Defects in this gene are a cause of type IIb congenital disorder of glycosylation (CDGIIb). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.