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C5ORF49 antibody (AA 1-100) (Biotin)

C5ORF49 Reactivity: Human WB, IHC (fro), IHC (p), ELISA Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1701475
  • Target See all C5ORF49 products
    C5ORF49 (Chromosome 5 Open Reading Frame 49 (C5ORF49))
    Binding Specificity
    AA 1-100
    Reactivity
    Human
    Host
    • 14
    Rabbit
    Clonality
    • 14
    Polyclonal
    Conjugate
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C5ORF49 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
    Predicted Reactivity
    Human,Mouse,Rat,Cow,Sheep,Pig,Horse
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C5orf49
    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
    C5ORF49 (Chromosome 5 Open Reading Frame 49 (C5ORF49))
    Alternative Name
    C5orf49 (C5ORF49 Products)
    Synonyms
    chromosome 5 open reading frame 49 antibody, C5orf49 antibody
    Background

    Synonyms: C5orf49, CE049_HUMAN, Chromosome 5 open reading frame 49, Uncharacterized protein C5orf49.

    Background: C5orf49 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf49 gene product has been provisionally designated C5orf49 pending further characterization.

    Gene ID
    134121
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