GCS1 (MOGS) (NM_006302) Human 3' UTR Clone
CAT#: SC202793
3' UTR clone of mannosyl-oligosaccharide glucosidase (MOGS) transcript variant 1 for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | MOGS |
Synonyms | CDG2B; CWH41; DER7; GCS1 |
ACCN | NM_006302 |
Insert Size | 248 bp |
Sequence Data |
>SC202793 3’UTR clone of NM_006302
The sequence shown below is from the reference sequence of NM_006302. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTCTTACTGGCCATGGCTGAAGACTACTGAAGGGAGGGAGAGGAGGGGAGCCAAGACACTCATGCCACT CTGGCTCTGAAGGGACAAAGGCTTCTGGCTTTTGCCCCCAGCCCCTTGGATACCAGTAATTCAAACCTT CCTCATTTCATCTCAGGTGTCTCCTTGCTGTCATCCCACATAGCCCTGGGGTGAATGTGAATCCAGAGT CTATTTTTCTAAATAAATTGGAAAAAACATTTTGAACTCTA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Product Components | The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. |
Reference Data | |
RefSeq | NM_006302.3 |
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] |
Locus ID | 7841 |
MW | 9.1 |
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