RAI2 (NM_021785) Human Recombinant Protein

• Background:

  Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]

• Synonyms:

  OTTHUMP00000022997; OTTHUMP00000022998; retinoic acid induced 2

• Gene ID:

  10742

• UniProt:

  Q9Y5P3, A0A024RBZ8, B3KPD7, B2RBE9

• Accession Number mRNA:

  NM_021785

• Chromosomal Location:

  Xp22.13

• Expression System:

  HEK293T

• Tag:

  C-Myc/DDK

• Concentration:

  >50 ug/mL as determined by microplate BCA method

• Purity:

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

• Form:

  Liquid

• Buffer:

  25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

• Molecular Weight:

  57 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:

  RAI2

• Species:

  Human

• Protein ID:

  NP_068557

• Overview:

  Recombinant protein of human retinoic acid induced 2 (RAI2)

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/10742

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q9Y5P3

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_021785

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_068557