ALG3 (NM_005787) Human Tagged ORF Clone

CAT#: RC201101L3

  • LentiORF®

Lenti ORF clone of Human asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog (S. cerevisiae) (ALG3), transcript variant 1, Myc-DDK-tagged


  "NM_005787" in other vectors (6)

Reconstitution Protocol

USD 620.00

3 Weeks*

Size
    • 10 ug

Product Images

Other products for "ALG3"

Specifications

Product Data
Type Human Tagged ORF Clone
Tag Myc-DDK
Symbol ALG3
Synonyms CDG1D; CDGS4; CDGS6; D16Ertd36e; not; Not56; NOT56L
Vector pLenti-C-Myc-DDK-P2A-Puro
E. coli Selection Chloramphenicol (34 ug/mL)
Mammalian Cell Selection Puromycin
Sequence Data
The ORF insert of this clone is exactly the same as(RC201101).
Restriction Sites SgfI-MluI      Cloning Scheme for this gene     
ACCN NM_005787
ORF Size 1314 bp
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_005787.4, NP_005778.1
RefSeq Size 1550
RefSeq ORF 1317
Locus ID 10195
Domains ALG3
Protein Families Transmembrane
Protein Pathways Metabolic pathways, N-Glycan biosynthesis
MW 50.1 kDa
Gene Summary This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]

Other Versions

{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.