GPD1L (NM_015141) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206131L3V

Lenti ORF particles, GPD1L (Myc-DDK tagged) - Human glycerol-3-phosphate dehydrogenase 1-like (GPD1L), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: GPD1L
• Synonyms: GPD1-L
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• ACCN: NM_015141
• ORF Size: 1053 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC206131).
• 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_015141.2, NP_055956.1
• RefSeq Size: 4068 bp
• RefSeq ORF: 1056 bp
• Locus ID: 23171
• UniProt ID: Q8N335
• Cytogenetics: 3p22.3
• Domains: NAD_Gly3P_dh
• Protein Pathways: Glycerophospholipid metabolism
• MW: 38.4 kDa
• Gene Summary: The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010]