CCDC22 (NM_014008) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC201585L2V

Lenti ORF particles, CCDC22 (mGFP-tagged) - Human coiled-coil domain containing 22 (CCDC22), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: CCDC22
• Synonyms: CXorf37; JM1; RTSC2
• Mammalian Cell Selection: None
• Vector: pLenti-C-mGFP
• ACCN: NM_014008
• ORF Size: 1881 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC201585).
• 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_014008.2
• RefSeq Size: 2333 bp
• RefSeq ORF: 1884 bp
• Locus ID: 28952
• UniProt ID: O60826
• Cytogenetics: Xp11.23
• MW: 70.8 kDa
• Gene Summary: This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]