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POU4F3 antibody

POU4F3 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7263711
  • Target See all POU4F3 Antibodies
    POU4F3 (POU Domain, Class 4, Transcription Factor 3 (POU4F3))
    Reactivity
    • 29
    • 12
    • 8
    • 5
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human
    Host
    • 22
    • 6
    • 1
    Rabbit
    Clonality
    • 26
    • 3
    Polyclonal
    Conjugate
    • 22
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This POU4F3 antibody is un-conjugated
    Application
    • 20
    • 11
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human POU4F3 (NP_002691.1).
    Isotype
    IgG
    Top Product
    Discover our top product POU4F3 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    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
    POU4F3 (POU Domain, Class 4, Transcription Factor 3 (POU4F3))
    Alternative Name
    POU4F3 (POU4F3 Products)
    Synonyms
    POU4F3 antibody, BRN-3 antibody, BRN3 antibody, BRN3C antibody, DFNA15 antibody, BRN-3.1 antibody, brn-3c antibody, brn3.1 antibody, brn3c antibody, Brn3.1 antibody, Brn3c antibody, ddl antibody, dreidel antibody, POU class 4 homeobox 3 antibody, POU domain, class 4, transcription factor 3 antibody, POU4F3 antibody, Pou4f3 antibody, pou4f3 antibody
    Background
    This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15.
    Molecular Weight

    Observed_MW: 37 kDa

    Calculated_MW: 37 kDa

    Gene ID
    5459
    UniProt
    Q15319
    Pathways
    Sensory Perception of Sound
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