FOXI1 (NM_144769) Human Recombinant Protein

• Background:

  This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4. [provided by RefSeq, Jan 2017]

• Synonyms:

  FKH10; FKHL10; FREAC-6; FREAC6; HFH-3; HFH3

• Gene ID:

  2299

• UniProt:

  Q12951

• Accession Number mRNA:

  NM_144769

• Chromosomal Location:

  5q35.1

• 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

• Function:

  Transcription Factors

• Molecular Weight:

  30.6 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:

  FOXI1

• Species:

  Human

• Protein ID:

  NP_658982

• Overview:

  Recombinant protein of human forkhead box I1 (FOXI1), transcript variant 2

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/2299

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q12951

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_144769

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_658982