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SOX10 antibody

This Rabbit Monoclonal antibody specifically detects SOX10 in WB, IF and IP. It exhibits reactivity toward Human.
Catalog No. ABIN7270567
-15% Promotion 2026
$310.25
$365.00
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Quick Overview for SOX10 antibody (ABIN7270567)

Target

See all SOX10 Antibodies
SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))

Reactivity

  • 128
  • 80
  • 45
  • 8
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 102
  • 50
  • 2
Rabbit

Clonality

  • 96
  • 58
Monoclonal

Conjugate

  • 62
  • 14
  • 7
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SOX10 antibody is un-conjugated

Application

  • 116
  • 63
  • 48
  • 41
  • 39
  • 22
  • 16
  • 15
  • 15
  • 13
  • 12
  • 10
  • 4
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP)
  • Purpose

    SOX10 Rabbit mAb

    Cross-Reactivity

    Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human SOX10

    Isotype

    IgG
  • Application Notes

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

    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

    SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))

    Alternative Name

    SOX10

    Background

    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 activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008],DOM, PCWH, WS2E, WS4, WS4C,Cell Biology & Developmental Biology,Cell Type Marker,Cell Type Marker_Neural Stem Cell marker,Epigenetics & Nuclear Signaling,Neuroscience,Stem Cells,Transcription Factors,SOX10

    Molecular Weight

    60kDa

    Gene ID

    6663

    UniProt

    P56693

    Pathways

    Chromatin Binding
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