CCDC22 (NM_014008) Human Recombinant Protein

CAT#: TP762464

Purified recombinant protein of Human coiled-coil domain containing 22 (CCDC22), full length, with N-terminal His tag, expressed in E.coli, 50ug

Product Images

Purified recombinant protein CCDC22 was analyzed by SDS-PAGE gel and Coomossie Blue Staining.

Specifications

Product Data

• Species: Human
• Expression Host: E. coli
• Expression cDNA Clone or AA Sequence:
  Protein Sequence

  A DNA sequence encoding the region full length of CCDC22
• Tag: N-His
• Predicted MW: 70.8 kDa
• Concentration: >0.05 µg/µL as determined by microplate BCA method
• Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining
• Buffer: 50 mM Tris-HCl, pH 8.0, 8 M urea
• Note: For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process.
• Storage: Store at -80°C after receiving vials.
• Stability: Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.

Reference Data

• RefSeq: NP_054727
• Locus ID: 28952
• UniProt ID: O60826, A0A024QZ03
• Cytogenetics: Xp11.23
• Refseq Size: 2333
• Refseq ORF: 1881
• Synonyms: CXorf37; JM1; RTSC2
• 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]