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FAM207A antibody (AA 95-120) (AbBy Fluor® 350)

FAM207A Reactivity: Human IF (p) Host: Rabbit Polyclonal AbBy Fluor® 350
Catalog No. ABIN1405743
  • Target See all FAM207A products
    FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))
    Binding Specificity
    • 14
    • 7
    • 1
    AA 95-120
    Reactivity
    • 22
    • 8
    • 1
    • 1
    • 1
    Human
    Host
    • 22
    Rabbit
    Clonality
    • 22
    Polyclonal
    Conjugate
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM207A antibody is conjugated to AbBy Fluor® 350
    Application
    • 12
    • 8
    • 7
    • 6
    • 4
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Cross-Reactivity
    Human
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C21orf70
    Isotype
    IgG
  • Application Notes
    IF(IHC-P) 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.
    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Expiry Date
    12 months
  • Target
    FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))
    Alternative Name
    C21orf70 (FAM207A Products)
    Synonyms
    C21orf70 antibody, 1810008A18Rik antibody, AI303072 antibody, family with sequence similarity 207 member A antibody, family with sequence similarity 207, member A antibody, FAM207A antibody, Fam207a antibody
    Background

    Synonyms: Chromosome 21 open reading frame 70, CU070_HUMAN, Hypothetical protein LOC85395, PRED56, Uncharacterized protein C21orf70.

    Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.

    Gene ID
    85395
    UniProt
    Q9NSI2
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