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Magic™ Membrane Protein Human FAR1 (Fatty acyl-CoA reductase 1) Full Length (CAT#: MPC3054K) Made to Order

This product is a made-to-order Human FAR1 membrane protein expressed in HEK293. The protein is for research use only and is not approved for use in humans or in clinical diagnosis.

Product Specifications

  • Host Species
  • Human
  • Target Protein
  • FAR1
  • Protein Length
  • Full length
  • Protein Class
  • Oxidoreductase
  • TMD
  • 1
  • Sequence
  • MVSIPEYYEGKNVLLTGATGFLGKVLLEKLLRSCPKVNSVYVLVRQKAGQ
    TPQERVEEVLSGKLFDRLRDENPDFREKIIAINSELTQPKLALSEEDKEV
    IIDSTNIIFHCAATVRFNENLRDAVQLNVIATRQLILLAQQMKNLEVFMH
    VSTAYAYCNRKHIDEVVYPPPVDPKKLIDSLEWMDDGLVNDITPKLIGDR
    PNTYIYTKALAEYVVQQEGAKLNVAIVRPSIVGASWKEPFPGWIDNFNGP
    SGLFIAAGKGILRTIRASNNALADLVPVDVVVNMSLAAAWYSGVNRPRNI
    MVYNCTTGSTNPFHWGEVEYHVISTFKRNPLEQAFRRPNVNLTSNHLLYH
    YWIAVSHKAPAFLYDIYLRMTGRSPRMMKTITRLHKAMVFLEYFTSNSWV
    WNTENVNMLMNQLNPEDKKTFNIDVRQLHWAEYIENYCLGTKKYVLNEEM
    SGLPAARKHLNKLRNIRYGFNTILVILIWRIFIARSQMARNIWYFVVSLC
    YKFLSYFRASSTMRY

Product Description

  • Expression Systems
  • HEK293
  • Tag
  • Flag-StrepII or based on specific requirements
  • Protein Format
  • Detergent or based on specific requirements (Detergent, Liposome, Nanodisc, SMALPs, VLP)

Target

  • Target Protein
  • FAR1
  • Full Name
  • Fatty acyl-CoA reductase 1
  • Introduction
  • The protein encoded by this gene is required for the reduction of fatty acids to fatty alcohols, a process that is required for the synthesis of monoesters and ether lipids. NADPH is required as a cofactor in this reaction, and 16-18 carbon saturated and unsaturated fatty acids are the preferred substrate. This is a peroxisomal membrane protein, and studies suggest that the N-terminus contains a large catalytic domain located on the outside of the peroxisome, while the C-terminus is exposed to the matrix of the peroxisome. Studies indicate that the regulation of this protein is dependent on plasmalogen levels. Mutations in this gene have been associated with individuals affected by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity (PMID: 25439727). A pseudogene of this gene is located on chromosome 13.
  • Alternative Names
  • FAR1; CSPSD; PFCRD; MLSTD2; SDR10E1; male sterility domain-containing protein 2; short chain dehydrogenase/reductase family 10E, member 1; Fatty acyl-CoA reductase 1

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