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SOX14 antibody

SOX14 Reactivity: Human, Mouse, Rat WB, IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6292418
  • Target See all SOX14 Antibodies
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    Reactivity
    • 31
    • 8
    • 7
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    Human, Mouse, Rat
    Host
    • 31
    Rabbit
    Clonality
    • 31
    Polyclonal
    Conjugate
    • 13
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SOX14 antibody is un-conjugated
    Application
    • 25
    • 13
    • 13
    • 10
    • 4
    • 3
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human SOX14
    Isotype
    IgG
    Top Product
    Discover our top product SOX14 Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    IHC 1:50 - 1:200
    IF 1:50 - 1:200
    Restrictions
    For Research Use only
  • 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 -20C. Avoid freeze / thaw cycles.
  • Target
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    Alternative Name
    SOX14 (SOX14 Products)
    Synonyms
    SOX28 antibody, zgc:123197 antibody, SRY-box 14 antibody, SRY-box 14 S homeolog antibody, SRY box 14 antibody, SRY (sex determining region Y)-box 14 antibody, SOX14 antibody, sox14.S antibody, Sox14 antibody, sox14 antibody
    Background
    This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.
    Molecular Weight
    26.485 kDa
    Gene ID
    8403
    UniProt
    O95416
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