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C2orf55 Antikörper (Cy3)

C2orf55 Reaktivität: Human, Ratte, Maus WB, IF (p) Wirt: Kaninchen Polyclonal Cy3
Produktnummer ABIN1422707
  • Target Alle C2orf55 Produkte
    C2orf55 (Chromosome 2 Open Reading Frame 55 (C2orf55))
    Reaktivität
    • 17
    • 15
    • 14
    • 2
    • 2
    • 1
    Human, Ratte, Maus
    Wirt
    • 17
    Kaninchen
    Klonalität
    • 17
    Polyklonal
    Konjugat
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser C2orf55 Antikörper ist konjugiert mit Cy3
    Applikation
    • 17
    • 12
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Kreuzreaktivität
    Human, Maus, Ratte
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C2orf55
    Isotyp
    IgG
  • Applikationshinweise
    IF(IHC-P) 1:50-200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    C2orf55 (Chromosome 2 Open Reading Frame 55 (C2orf55))
    Andere Bezeichnung
    C2orf55 (C2orf55 Produkte)
    Synonyme
    C2orf55 antikoerper, KIAA1211 like antikoerper, KIAA1211L antikoerper
    Hintergrund

    Synonyms: Chromosome 2 open reading frame 55, Hypothetical protein LOC343990, K121L_HUMAN.

    Background: C2orf55, also known as MGC42367, is a 962 amino acid protein that is encoded by a gene located on human chromosome 2q11.2. The second largest human chromosome, chromosome 2 consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

    Gen-ID
    343990
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