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C6ORF132 antibody (AA 1001-1188) (Biotin)

C6ORF132 Reactivity: Human WB, IHC (fro), IHC (p), ELISA Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1700842
  • Target See all C6ORF132 products
    C6ORF132 (Chromosome 6 Open Reading Frame 132 (C6ORF132))
    Binding Specificity
    AA 1001-1188
    Reactivity
    Human
    Host
    • 14
    Rabbit
    Clonality
    • 14
    Polyclonal
    Conjugate
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C6ORF132 antibody is conjugated to Biotin
    Application
    • 14
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
    Cross-Reactivity
    Human
    Predicted Reactivity
    Mouse,Rat,Cow,Sheep,Rabbit
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C6orf132
    Isotype
    IgG
  • Application Notes
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    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.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C for 12 months.
    Expiry Date
    12 months
  • Target
    C6ORF132 (Chromosome 6 Open Reading Frame 132 (C6ORF132))
    Alternative Name
    C6orf132 (C6ORF132 Products)
    Synonyms
    bA7K24.2 antibody, chromosome 6 open reading frame 132 antibody, C6orf132 antibody
    Background

    Synonyms: bA7K24.2, C6orf132, CF132_HUMAN, Chromosome 6 open reading frame 132, Uncharacterized protein C6orf132.

    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 C6orf132 gene product has been provisionally designated C6orf132 pending further characterization.

    Gene ID
    647024
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