D2HGDH (NM_152783) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC207367L2V

Lenti ORF particles, D2HGDH (mGFP-tagged) - Human D-2-hydroxyglutarate dehydrogenase (D2HGDH), nuclear gene encoding mitochondrial protein, 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: D2HGDH
• Synonyms: D2HGD
• Mammalian Cell Selection: None
• Vector: pLenti-C-mGFP
• ACCN: NM_152783
• ORF Size: 1563 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC207367).
• 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_152783.3, NP_689996.3
• RefSeq Size: 2660 bp
• RefSeq ORF: 1566 bp
• Locus ID: 728294
• UniProt ID: Q8N465
• Cytogenetics: 2q37.3
• MW: 56.4 kDa
• Gene Summary: This gene encodes D-2hydroxyglutarate dehydrogenase, a mitochondrial enzyme belonging to the FAD-binding oxidoreductase/transferase type 4 family. This enzyme, which is most active in liver and kidney but also active in heart and brain, converts D-2-hydroxyglutarate to 2-ketoglutarate. Mutations in this gene are present in D-2-hydroxyglutaric aciduria, a rare recessive neurometabolic disorder causing developmental delay, epilepsy, hypotonia, and dysmorphic features. [provided by RefSeq, Jul 2008]