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C19orf54 antibody (Cy5)

C19orf54 Reactivity: Human WB, IF (p) Host: Rabbit Polyclonal Cy5
Catalog No. ABIN1421940
  • Target See all C19orf54 products
    C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))
    Reactivity
    Human
    Host
    • 16
    Rabbit
    Clonality
    • 16
    Polyclonal
    Conjugate
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C19orf54 antibody is conjugated to Cy5
    Application
    • 16
    • 12
    • 3
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Cross-Reactivity
    Human
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C19orf54
    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
    C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))
    Alternative Name
    C19orf54 (C19orf54 Products)
    Synonyms
    C19H19orf54 antibody, chromosome 19 open reading frame 54 antibody, chromosome 19 open reading frame, human C19orf54 antibody, C19orf54 antibody, C19H19orf54 antibody, c19orf54 antibody
    Background

    Synonyms: Chromosome 19 open reading frame 54, FLJ17063, FLJ41131, Hypothetical protein LOC284325, MGC103014, UPF0692 protein C19orf54, CS054_HUMAN.

    Background: C19orf54 is a 351 amino acid protein that exists as two alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

    Gene ID
    284325
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