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C9ORF135 Antikörper (AA 151-229) (Biotin)

C9ORF135 Reaktivität: Human WB, IHC (fro), IHC (p), ELISA Wirt: Kaninchen Polyclonal Biotin
Produktnummer ABIN1700230
  • Target Alle C9ORF135 Produkte
    C9ORF135 (Chromosome 9 Open Reading Frame 135 (C9ORF135))
    Bindungsspezifität
    • 14
    • 1
    AA 151-229
    Reaktivität
    Human
    Wirt
    • 15
    Kaninchen
    Klonalität
    • 15
    Polyklonal
    Konjugat
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser C9ORF135 Antikörper ist konjugiert mit Biotin
    Applikation
    • 15
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
    Homologie
    Human,Mouse,Rat,Horse,Rabbit
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C9orf135
    Isotyp
    IgG
  • Applikationshinweise
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    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 for 12 months.
    Haltbarkeit
    12 months
  • Target
    C9ORF135 (Chromosome 9 Open Reading Frame 135 (C9ORF135))
    Andere Bezeichnung
    C9orf135 (C9ORF135 Produkte)
    Synonyme
    chromosome 9 open reading frame 135 antikoerper, C9orf135 antikoerper
    Hintergrund

    Synonyms: C9orf135, CI135_HUMAN, Uncharacterized protein C9orf135.

    Background: C9orf135 (chromosome 9 open reading frame 135) is a 229 amino acid single-pass membrane protein encoded by a gene that maps to human chromosome 9q21.11. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

    Gen-ID
    138724
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