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FBXW4 Antikörper (C-Term)

FBXW4 Reaktivität: Human WB Wirt: Kaninchen Polyclonal RB42400 unconjugated
Produktnummer ABIN1881340
  • Target Alle FBXW4 Antikörper anzeigen
    FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
    Bindungsspezifität
    • 13
    • 13
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 341-370, C-Term
    Reaktivität
    • 32
    • 12
    • 10
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    Human
    Wirt
    • 34
    • 2
    Kaninchen
    Klonalität
    • 36
    Polyklonal
    Konjugat
    • 17
    • 5
    • 4
    • 4
    • 3
    • 3
    Dieser FBXW4 Antikörper ist unkonjugiert
    Applikation
    • 29
    • 27
    • 9
    • 4
    • 3
    • 3
    Western Blotting (WB)
    Aufreinigung
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    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.
    Klon
    RB42400
    Isotyp
    Ig Fraction
    Top Product
    Discover our top product FBXW4 Primärantikörper
  • Applikationshinweise
    WB: 1:1000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Haltbarkeit
    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." in: 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. ..." in: Nature, Vol. 429, Issue 6990, pp. 375-81, (2004) (PubMed).

  • Target
    FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
    Andere Bezeichnung
    FBXW4 (FBXW4 Produkte)
    Synonyme
    dac antikoerper, hag antikoerper, hagoromo antikoerper, wu:fk63g06 antikoerper, FBXW4 antikoerper, DAC antikoerper, FBW4 antikoerper, FBWD4 antikoerper, SHFM3 antikoerper, SHSF3 antikoerper, Dac antikoerper, Fbw4 antikoerper, dactylin antikoerper, dactylyn antikoerper, F-box and WD repeat domain containing 4 antikoerper, F-box and WD-40 domain protein 4 antikoerper, fbxw4 antikoerper, FBXW4 antikoerper, Fbxw4 antikoerper
    Hintergrund
    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.
    Molekulargewicht
    46337
    NCBI Accession
    NP_071322
    UniProt
    P57775
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