CCNQ (NM_152274) Human Recombinant Protein

• Background:

  Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

• Synonyms:

  CycM; FAM58A

• Gene ID:

  92002

• UniProt:

  Q8N1B3

• Accession Number mRNA:

  NM_152274

• Chromosomal Location:

  Xq28

• Expression System:

  E. coli

• Tag:

  N-GST and C-His

• Concentration:

  >50 ug/mL as determined by microplate BCA method

• Purity:

  > 80% as determined by SDS-PAGE and Coomassie blue staining

• Form:

  Liquid

• Buffer:

  50mM Tris, pH8.0, 8M Urea.

• Molecular Weight:

  52.7 kDa

• Storage Conditions:

  Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.

• Symbol:

  CCNQ

• Species:

  Human

• Protein ID:

  NP_689487

• Overview:

  Purified recombinant protein of Human family with sequence similarity 58, member A (FAM58A), transcript variant 1, full length, with N-terminal GST and C-terminal His tag, expressed in E. coli, 50ug

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/92002

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q8N1B3

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_152274

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_689487