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DPCD antibody

DPCD Reactivity: Human, Mouse, Rat ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7248540
  • Target See all DPCD Antibodies
    DPCD (Deleted in Primary Ciliary Dyskinesia Homolog (DPCD))
    Reactivity
    • 23
    • 14
    • 6
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human, Mouse, Rat
    Host
    • 21
    • 2
    Rabbit
    Clonality
    • 21
    • 2
    Polyclonal
    Conjugate
    • 13
    • 2
    • 2
    • 2
    • 2
    • 2
    This DPCD antibody is un-conjugated
    Application
    • 22
    • 14
    • 4
    • 2
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human DPCD
    Isotype
    IgG
    Top Product
    Discover our top product DPCD Primary Antibody
  • Application Notes
    IHC 1:50-1:100, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.5 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
    DPCD (Deleted in Primary Ciliary Dyskinesia Homolog (DPCD))
    Alternative Name
    DPCD (DPCD Products)
    Synonyms
    RP11-529I10.4 antibody, zgc:153412 antibody, rp11-529i10.4 antibody, 5330431N19Rik antibody, Ndac antibody, RGD1307648 antibody, deleted in primary ciliary dyskinesia homolog (mouse) antibody, deleted in a mouse model of primary ciliary dyskinesia S homeolog antibody, deleted in primary ciliary dyskinesia antibody, DPCD antibody, dpcd antibody, dpcd.S antibody, Dpcd antibody
    Background
    This gene in mouse encodes a protein that may be involved in the generation and maintenance of ciliated cells. In mouse, expression of this gene increases during ciliated cell differentiation, and disruption of this gene has been linked to primary ciliary dyskinesia.
    UniProt
    Q9BVM2
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