FBXW4 polyclonal antibody (A01)

Catalog # H00006468-A01

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Size:50 uL
Price: USD $ 243.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Western Blot detection against Immunogen (37.11 KDa) .

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a partial recombinant FBXW4.

    Immunogen

    FBXW4 (NP_071322, 41 a.a. ~ 140 a.a) partial recombinant protein with GST tag.

    Sequence

    SYLDMRALGRLAQVCRWLRRFTSCDLLWRRIARASLNSGFTRLGTDLMTSVPVKERVKVSQNWRLGRCREGILLKWRCSQMPWMQLEDDSLYISQANFIL

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (87); Rat (92)

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (37.11 KDa) .

    Storage Buffer

    50 % glycerol

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — FBXW4

    Entrez GeneID

    6468

    GeneBank Accession#

    NM_022039

    Protein Accession#

    NP_071322

    Gene Name

    FBXW4

    Gene Alias

    DAC, FBW4, FBWD4, SHFM3, SHSF3

    Gene Description

    F-box and WD repeat domain containing 4

    Omim ID

    600095 608071

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the F-box/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein binding domains for ubiquitin mediated degradation. In mouse, a highly similar protein is thought to be responsible for maintaining the apical ectodermal ridge of developing limb buds; disruption of the mouse gene results in the absence of central digits, underdeveloped or absent metacarpal/metatarsal bones and syndactyly. This phenotype is remarkably similar to split hand-split foot malformation in humans, a clinically heterogeneous condition with a variety of modes of transmission. An autosomal recessive form has been mapped to the chromosomal region where this gene is located, and complex rearrangements involving duplications of this gene and others have been associated with the condition. A pseudogene of this locus has been mapped to one of the introns of the BCR gene on chromosome 22. [provided by RefSeq

    Other Designations

    F-box and WD-40 domain protein 4|F-box/WD repeat protein 4|OTTHUMP00000059175|dactylin

  • Interactome
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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