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DGCR6L antibody

DGCR6L Reactivity: Human WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7246901
  • Target See all DGCR6L Antibodies
    DGCR6L (DiGeorge Syndrome Critical Region Gene 6-Like (DGCR6L))
    Reactivity
    • 40
    • 19
    • 18
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human
    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
    • 17
    • 13
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human DGCR6L
    Isotype
    IgG
  • Application Notes
    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.14 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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)
    Background
    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: Refer to figures

    Calculated_MW: 25 kDa

    UniProt
    Q9BY27
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