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DGCR6L antibody

DGCR6L Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7384056
  • Target See all DGCR6L Antibodies
    DGCR6L (DiGeorge Syndrome Critical Region Gene 6-Like (DGCR6L))
    Reactivity
    • 40
    • 18
    • 17
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 39
    • 1
    Rabbit
    Clonality
    • 40
    Polyclonal
    Conjugate
    • 12
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DGCR6L antibody is un-conjugated
    Application
    • 36
    • 18
    • 13
    • 3
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human DGCR6L (NP_150282.2).
    Isotype
    IgG
    Top Product
    Discover our top product DGCR6L Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    DGCR6L (DiGeorge Syndrome Critical Region Gene 6-Like (DGCR6L))
    Alternative Name
    DGCR6L (DGCR6L Products)
    Synonyms
    DGCR6L antibody, DiGeorge syndrome critical region gene 6-like antibody, DiGeorge syndrome critical region gene 6 like antibody, DGCR6L antibody
    Background
    DGCR6L,DGCR6,This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns. The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration. This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome.
    Molecular Weight

    Observed_MW: 25 kDa

    Calculated_MW: 24 kDa

    Gene ID
    85359
    UniProt
    Q9BY27
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