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C6orf168 anticorps (AA 221-320) (Cy3)

FAXC Reactivité: Humain WB, IF (cc), IF (p) Hôte: Lapin Polyclonal Cy3
N° du produit ABIN1703006
  • Antigène Voir toutes C6orf168 (FAXC) Anticorps
    C6orf168 (FAXC) (Failed Axon Connections Homolog (Drosophila) (FAXC))
    Épitope
    • 14
    • 1
    AA 221-320
    Reactivité
    • 16
    • 1
    • 1
    Humain
    Hôte
    • 16
    Lapin
    Clonalité
    • 16
    Polyclonal
    Conjugué
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp C6orf168 est conjugé à/à la Cy3
    Application
    • 15
    • 12
    • 12
    • 4
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Homologie
    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human C6orf168
    Isotype
    IgG
    Top Product
    Discover our top product FAXC Anticorps primaire
  • Indications d'application
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Date de péremption
    12 months
  • Antigène
    C6orf168 (FAXC) (Failed Axon Connections Homolog (Drosophila) (FAXC))
    Autre désignation
    C6orf168 (FAXC Produits)
    Synonymes
    anticorps C6orf168, anticorps dJ273F20, anticorps failed axon connections homolog, anticorps FAXC
    Sujet

    Synonyms: C6orf168, CF168_HUMAN, Chromosome 6 open reading frame 168, dJ273F20, Uncharacterized protein C6orf168.

    Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf168 gene product has been provisionally designated C6orf168 pending further characterization.

    ID gène
    84553
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