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Magic™ Membrane Protein Human FZD9 (Frizzled class receptor 9) Full Length (CAT#: MPC0104K) Made to Order

This product is a 64.4 kDa Human FZD9 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
  • FZD9
  • Protein Length
  • Full length
  • Protein Class
  • GPCR
  • Molecular Weight
  • 64.4 kDa
  • TMD
  • 7
  • Sequence
  • MAVAPLRGALLLWQLLAAGGAALEIGRFDPERGRGAAPCQAVEIPMCRGI
    GYNLTRMPNLLGHTSQGEAAAELAEFAPLVQYGCHSHLRFFLCSLYAPMC
    TDQVSTPIPACRPMCEQARLRCAPIMEQFNFGWPDSLDCARLPTRNDPHA
    LCMEAPENATAGPAEPHKGLGMLPVAPRPARPPGDLGPGAGGSGTCENPE
    KFQYVEKSRSCAPRCGPGVEVFWSRRDKDFALVWMAVWSALCFFSTAFTV
    LTFLLEPHRFQYPERPIIFLSMCYNVYSLAFLIRAVAGAQSVACDQEAGA
    LYVIQEGLENTGCTLVFLLLYYFGMASSLWWVVLTLTWFLAAGKKWGHEA
    IEAHGSYFHMAAWGLPALKTIVILTLRKVAGDELTGLCYVASTDAAALTG
    FVLVPLSGYLVLGSSFLLTGFVALFHIRKIMKTGGTNTEKLEKLMVKIGV
    FSILYTVPATCVIVCYVYERLNMDFWRLRATEQPCAAAAGPGGRRDCSLP
    GGSVPTVAVFMLKIFMSLVVGITSGVWVWSSKTFQTWQSLCYRKIAAGRA
    RAKACRAPGSYGRGTHCHYKAPTVVLHMTKTDPSLENPTHL

Product Description

  • Expression Systems
  • HEK293
  • Tag
  • Flag-StrepII or based on specific requirements
  • Protein Format
  • Detergent or based on specific requirements

Target

  • Target Protein
  • FZD9
  • Full Name
  • Frizzled class receptor 9
  • Introduction
  • Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.
  • Alternative Names
  • frizzled 9, seven transmembrane spanning receptor; frizzled family receptor 9; frizzled homolog 9; fz-9; fzE6; hFz9; FZD3; CD349; frizzled-9; FZD9; Frizzled class receptor 9

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