SLC29A3 (NM_018344) Human Tagged ORF Clone Lentiviral Particle

SKU RC217319L2V

Lenti ORF particles, SLC29A3 (mGFP-tagged) - Human solute carrier family 29 (nucleoside transporters), member 3 (SLC29A3), transcript variant 1, 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Target Symbol: SLC29A3
• Synonyms: ENT3; HCLAP; HJCD; PHID
• Vector: pLenti-C-mGFP
• Mammalian Cell Selection: None
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC217319).
• ACCN: NM_018344
• ORF Size: 1425 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_018344.3
• RefSeq Size: 2277 bp
• RefSeq ORF: 1428 bp
• Locus ID: 55315
• UniProt ID: Q9BZD2
• Cytogenetics: 10q22.1
• Domains: Nucleoside_tran
• Protein Families: Transmembrane
• MW: 51.9 kDa
• Summary: This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2010]