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SOX18 antibody (AA 63-362)

The Rabbit Polyclonal anti-SOX18 antibody is suitable to detect SOX18 in samples from Human, Mouse and Rat. It has been validated for WB, ELISA, IF and FACS.
Catalog No. ABIN7876236
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SOX18 antibody (AA 63-362) (ABIN7876236)

Target

See all SOX18 Antibodies
SOX18 (SRY (Sex Determining Region Y)-Box 18 (SOX18))

Reactivity

  • 48
  • 21
  • 17
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 44
  • 7
Rabbit

Clonality

  • 28
  • 23
Polyclonal

Conjugate

  • 23
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SOX18 antibody is un-conjugated

Application

  • 32
  • 16
  • 13
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Binding Specificity

    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 63-362

    Purpose

    SOX18 Antibody

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids E63-E362) was used as the immunogen for the SOX18 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the SOX18 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the SOX18 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    SOX18 (SRY (Sex Determining Region Y)-Box 18 (SOX18))

    Alternative Name

    SOX18

    Background

    Transcription factor SOX-18 is a protein that in humans is encoded by the SOX18 gene. This 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. This protein plays a role in hair, blood vessel, and lymphatic vessel development. Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.

    UniProt

    P35713
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