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C19orf21 antibody (Cy3)

MISP Reactivity: Human, Mouse, Rat WB, IF (p) Host: Rabbit Polyclonal Cy3
Catalog No. ABIN1421903
  • Target See all C19orf21 (MISP) products
    C19orf21 (MISP) (Mitotic Spindle Positioning (MISP))
    Reactivity
    • 32
    • 16
    • 16
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 32
    Rabbit
    Clonality
    • 32
    Polyclonal
    Conjugate
    • 8
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C19orf21 antibody is conjugated to Cy3
    Application
    • 32
    • 13
    • 13
    • 13
    • 12
    • 5
    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 C19orf21
    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
    C19orf21 (MISP) (Mitotic Spindle Positioning (MISP))
    Alternative Name
    C19orf21 (MISP Products)
    Synonyms
    C19orf21 antibody, 9130017N09Rik antibody, mitotic spindle positioning antibody, MISP antibody, Misp antibody
    Background

    Synonyms: chromosome 19 open reading frame 21, hypothetical protein LOC126353, Uncharacterized protein C19orf21, CS021_HUMAN.

    Background: C19orf21 is a 679 amino acid protein that is 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
    126353
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