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C21orf62 antibody (FITC)

C21orf62 Reactivity: Human, Rat, Mouse WB, IF (p) Host: Rabbit Polyclonal FITC
Catalog No. ABIN1405724
  • Target See all C21orf62 products
    C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))
    Reactivity
    Human, Rat, Mouse
    Host
    • 16
    • 2
    Rabbit
    Clonality
    • 16
    • 2
    Polyclonal
    Conjugate
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C21orf62 antibody is conjugated to FITC
    Application
    • 17
    • 12
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Cross-Reactivity
    Human, Mouse, Rat
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C21ORF62
    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
    C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))
    Alternative Name
    C21ORF62 (C21orf62 Products)
    Synonyms
    B37 antibody, PRED81 antibody, C21orf120 antibody, MGC88933 antibody, chromosome 21 open reading frame 62 antibody, chromosome 1 open reading frame, human C21orf62 antibody, chromosome 3 open reading frame, human C21orf62 antibody, C21orf62 antibody, C1H21ORF62 antibody, c21orf62 antibody, C3H21orf62 antibody
    Background

    Synonyms: B37, C21orf120, Chromosome 21 open reading frame 62, Hypothetical protein LOC56245, PRED81, Uncharacterized protein C21orf62, CU062_HUMAN.

    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 C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.

    Gene ID
    56245
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