GALNT17 (NM_022479) Human Tagged ORF Clone

CAT#: RC212796L4

Lenti ORF clone of Human Williams-Beuren syndrome chromosome region 17 (WBSCR17), mGFP tagged

Specifications

Product Data

• Type: Human Tagged ORF Clone
• Tag: mGFP
• Symbol: GALNT17
• Synonyms: GalNAc-T5L; GalNAc-T17; GalNAc-T19; GALNACT17; GALNT16; GALNT20; GALNTL3; WBSCR17
• Vector: pLenti-C-mGFP-P2A-Puro
• E. coli Selection: Chloramphenicol (34 ug/mL)
• Mammalian Cell Selection: Puromycin
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC212796).
• Restriction Sites: SgfI-MluI Cloning Scheme for this gene
• 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.

Reference Data

• RefSeq: NM_022479.1, NP_071924.1
• RefSeq Size: 3298
• RefSeq ORF: 1797
• Locus ID: 64409
• Domains: RICIN, Glycos_transf_2
• Protein Families: Transmembrane
• Protein Pathways: Metabolic pathways, O-Glycan biosynthesis
• MW: 67.6 kDa
• Gene 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]