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RBFA antibody

RBFA Reactivity: Human, Mouse, Rat WB, IF (p), IHC (p) Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1385454
  • Target See all RBFA Antibodies
    RBFA (Ribosome Binding Factor A (RBFA))
    Reactivity
    Human, Mouse, Rat
    Host
    • 10
    • 2
    Rabbit
    Clonality
    • 12
    Polyclonal
    Conjugate
    • 8
    • 2
    • 1
    • 1
    This RBFA antibody is un-conjugated
    Application
    • 8
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Cross-Reactivity
    Human, Mouse, Rat
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human RBFA
    Isotype
    IgG
    Top Product
    Discover our top product RBFA Primary Antibody
  • Application Notes
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
    4 °C,-20 °C
    Storage Comment
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Expiry Date
    12 months
  • Target
    RBFA (Ribosome Binding Factor A (RBFA))
    Alternative Name
    RBFA (RBFA Products)
    Synonyms
    C18orf22 antibody, HsT169 antibody, 1110032A13Rik antibody, AI595940 antibody, RGD1311910 antibody, zgc:162590 antibody, ribosome binding factor A antibody, RBFA antibody, Rbfa antibody, rbfa antibody
    Background

    Synonyms: mitochondrial, C18orf25, Chromosome 18 open reading frame 22, HsT169, Hypothetical protein LOC79863, Putative ribosome binding factor A, mitochondrial precursor, Putative ribosome-binding factor A, rbfA, RBFA_HUMAN.

    Background: C18orf22, also known as HsT169, is a 343 amino acid protein that localizes to the mitochondrion and is expressed as two alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

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