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SOX10 antibody (AA 200-300)

The Rabbit Polyclonal anti-SOX10 antibody has been validated for WB, IF and IHC. It is suitable to detect SOX10 in samples from Human.
Catalog No. ABIN7270568

Quick Overview for SOX10 antibody (AA 200-300) (ABIN7270568)

Target

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

Reactivity

  • 102
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Human

Host

  • 72
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Rabbit

Clonality

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  • 48
Polyclonal

Conjugate

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This SOX10 antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
  • Binding Specificity

    • 56
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    AA 200-300

    Purpose

    SOX10 Rabbit pAb

    Sequence

    TAAIQAHYKS AHLDHRHPGE GSPMSDGNPE HPSGQSHGPP TPPTTPKTEL QSGKADPKRD GRSMGEGGKP HIDFGNVDIG EISHEVMSNM ETFDVAELDQ Y

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic peptide corresponding to a sequence within amino acids 200-300 of human SOX10 (NP_008872.1).

    Isotype

    IgG
  • Application Notes

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

    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.,SOX10,DOM,PCWH,WS2E,WS4,WS4C,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,Neuroscience,Cell Type Marker,Stem Cells,Neural Stem Cell marker,SOX10

    Molecular Weight

    31kDa/49kDa

    Gene ID

    6663

    UniProt

    P56693

    Pathways

    Chromatin Binding
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