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VSX2 antibody

VSX2 Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7271331
  • Target See all VSX2 Antibodies
    VSX2 (Visual System Homeobox 2 (VSX2))
    Reactivity
    • 35
    • 17
    • 7
    • 1
    Human
    Host
    • 38
    • 5
    • 1
    Rabbit
    Clonality
    • 44
    Monoclonal
    Conjugate
    • 21
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This VSX2 antibody is un-conjugated
    Application
    • 37
    • 16
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    CHX10 Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human CHX10
    Isotype
    IgG
    Top Product
    Discover our top product VSX2 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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
    VSX2 (Visual System Homeobox 2 (VSX2))
    Alternative Name
    VSX2 (VSX2 Products)
    Synonyms
    CHX10 antibody, HOX10 antibody, MCOP2 antibody, MCOPCB3 antibody, RET1 antibody, Chx10 antibody, Hox-10 antibody, Hox10 antibody, or antibody, VSX2 antibody, Vsx-2 antibody, alx antibody, chx10 antibody, c-ret antibody, cret antibody, etID315074.13 antibody, ret1 antibody, wu:fd13h01 antibody, visual system homeobox 2 antibody, ret proto-oncogene receptor tyrosine kinase antibody, Vsx2 transcription factor antibody, VSX2 antibody, Vsx2 antibody, vsx2 antibody, ret antibody
    Background
    This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities. [provided by RefSeq, Oct 2009],CHX10, HOX10, MCOP2, MCOPCB3, RET1,Epigenetics & Nuclear Signaling,Neuroscience,Transcription Factors,VSX2
    Molecular Weight
    50kDa
    Gene ID
    338917
    UniProt
    P58304
    Pathways
    Dopaminergic Neurogenesis
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