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FAM13B antibody

FAM13B Reactivity: Human, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7243301
  • Target See all FAM13B products
    FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
    Reactivity
    Human, Mouse
    Host
    • 36
    • 1
    Rabbit
    Clonality
    • 37
    Polyclonal
    Conjugate
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM13B antibody is un-conjugated
    Application
    • 30
    • 15
    • 13
    • 13
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human FAM13B
    Isotype
    IgG
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
    Alternative Name
    FAM13B (FAM13B Products)
    Synonyms
    ARHGAP49 antibody, C5orf5 antibody, FAM13B1 antibody, KHCHP antibody, N61 antibody, 2610024E20Rik antibody, AW060714 antibody, AW546153 antibody, family with sequence similarity 13 member B antibody, family with sequence similarity 13, member B antibody, FAM13B antibody, Fam13b antibody
    Background
    FAM13B is a 915 amino acid protein that is encoded by a gene that maps to human chromosome 5. 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.
    NCBI Accession
    NP_057687
    UniProt
    Q9NYF5
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