WBSCR17 (GALNT17) (NM_022479) Human Tagged ORF Clone Lentiviral Particle

SKU RC212796L3V

Lenti ORF particles, WBSCR17 (Myc-DDK tagged) - Human Williams-Beuren syndrome chromosome region 17 (WBSCR17), 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Target Symbol: GALNT17
• Synonyms: GalNAc-T5L; GalNAc-T17; GalNAc-T19; GALNACT17; GALNT16; GALNT20; GALNTL3; WBSCR17
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• Mammalian Cell Selection: Puromycin
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC212796).
• ACCN: NM_022479
• ORF Size: 1794 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.
• Shipping: Dry Ice

Reference Data

• RefSeq: NM_022479.1
• RefSeq Size: 3298 bp
• RefSeq ORF: 1797 bp
• Locus ID: 64409
• UniProt ID: Q6IS24
• Cytogenetics: 7q11.22
• Domains: Glycos_transf_2, RICIN
• Protein Families: Transmembrane
• Protein Pathways: Metabolic pathways, O-Glycan biosynthesis
• MW: 67.6 kDa
• Summary: This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]