RFXDC1 (RFX6) (NM_173560) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206174L4V

Lenti ORF particles, RFX6 (mGFP-tagged) - Human regulatory factor X, 6 (RFX6), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: RFXDC1
• Synonyms: dJ955L16.1; MTCHRS; MTFS; RFXDC1
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_173560
• ORF Size: 2784 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC206174).
• 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_173560.1, NP_775831.1
• RefSeq Size: 3517 bp
• RefSeq ORF: 2787 bp
• Locus ID: 222546
• UniProt ID: Q8HWS3
• Cytogenetics: 6q22.1
• Protein Families: Transcription Factors
• MW: 102.4 kDa
• Gene Summary: The nuclear protein encoded by this gene is a member of the regulatory factor X (RFX) family of transcription factors. Studies in mice suggest that this gene is specifically required for the differentiation of islet cells for the production of insulin, but not for the differentiation of pancreatic polypeptide-producing cells. It regulates the transcription factors involved in beta-cell maturation and function, thus, restricting the expression of the beta-cell differentiation and specification genes. Mutations in this gene are associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis.[provided by RefSeq, Sep 2010]