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SOX14 antibody (AA 91-240)

This Rabbit Polyclonal antibody specifically detects SOX14 in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN6148290

Quick Overview for SOX14 antibody (AA 91-240) (ABIN6148290)

Target

See all SOX14 Antibodies
SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))

Reactivity

  • 30
  • 7
  • 6
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
Human

Host

  • 30
Rabbit

Clonality

  • 30
Polyclonal

Conjugate

  • 12
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SOX14 antibody is un-conjugated

Application

  • 24
  • 13
  • 13
  • 11
  • 4
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 15
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 91-240

    Sequence

    RYVFPLPYLG DTDPLKAAGL PVGASDGLLS APEKARAFLP PASAPYSLLD PAQFSSSAIQ KMGEVPHTLA TGALPYASTL GYQNGAFGSL SCPSQHTHTH PSPTNPGYVV PCNCTAWSAS TLQPPVAYIL FPGMTKTGID PYSSAHATAM

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 91-240 of human SOX14 (NP_004180.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))

    Alternative Name

    SOX14

    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.,SOX14,SOX28,Epigenetics & Nuclear Signaling,Transcription Factors,Signal Transduction,Neuroscience,SOX14

    Molecular Weight

    26 kDa

    Gene ID

    8403

    UniProt

    O95416
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