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FBXW4 anticorps (C-Term)

FBXW4 Reactivité: Humain WB Hôte: Lapin Polyclonal RB42400 unconjugated
N° du produit ABIN1881340
  • Antigène Voir toutes FBXW4 Anticorps
    FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
    Épitope
    • 13
    • 13
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 341-370, C-Term
    Reactivité
    • 32
    • 12
    • 10
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    Humain
    Hôte
    • 34
    • 2
    Lapin
    Clonalité
    • 36
    Polyclonal
    Conjugué
    • 17
    • 5
    • 4
    • 4
    • 3
    • 3
    Cet anticorp FBXW4 est non-conjugé
    Application
    • 29
    • 27
    • 9
    • 4
    • 3
    • 3
    Western Blotting (WB)
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogène
    This FBXW4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 341-370 amino acids from the C-terminal region of human FBXW4.
    Clone
    RB42400
    Isotype
    Ig Fraction
    Top Product
    Discover our top product FBXW4 Anticorps primaire
  • Indications d'application
    WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Date de péremption
    6 months
  • Everman, Morgan, Lyle, Laughridge, Bamshad, Clarkson, Colby, Gurrieri, Innes, Roberson, Schrander-Stumpel, van Bokhoven, Antonarakis, Schwartz: "Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation." dans: American journal of medical genetics. Part A, Vol. 140, Issue 13, pp. 1375-83, (2006) (PubMed).

    Deloukas, Earthrowl, Grafham, Rubenfield, French, Steward, Sims, Jones, Searle, Scott, Howe, Hunt, Andrews, Gilbert, Swarbreck, Ashurst, Taylor, Battles, Bird, Ainscough, Almeida, Ashwell, Ambrose et al.: "The DNA sequence and comparative analysis of human chromosome 10. ..." dans: Nature, Vol. 429, Issue 6990, pp. 375-81, (2004) (PubMed).

  • Antigène
    FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
    Autre désignation
    FBXW4 (FBXW4 Produits)
    Synonymes
    anticorps dac, anticorps hag, anticorps hagoromo, anticorps wu:fk63g06, anticorps FBXW4, anticorps DAC, anticorps FBW4, anticorps FBWD4, anticorps SHFM3, anticorps SHSF3, anticorps Dac, anticorps Fbw4, anticorps dactylin, anticorps dactylyn, anticorps F-box and WD repeat domain containing 4, anticorps F-box and WD-40 domain protein 4, anticorps fbxw4, anticorps FBXW4, anticorps Fbxw4
    Sujet
    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.
    Poids moléculaire
    46337
    NCBI Accession
    NP_071322
    UniProt
    P57775
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