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SOX10 antibody (AA 178-301)

This Rabbit Polyclonal antibody specifically detects SOX10 in WB, FACS, IF, ELISA and ICC. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7600305

Quick Overview for SOX10 antibody (AA 178-301) (ABIN7600305)

Target

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

Reactivity

  • 107
  • 70
  • 35
  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 76
  • 52
  • 2
Rabbit

Clonality

  • 81
  • 49
Polyclonal

Conjugate

  • 60
  • 10
  • 6
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SOX10 antibody is un-conjugated

Application

  • 107
  • 54
  • 38
  • 35
  • 29
  • 23
  • 17
  • 15
  • 13
  • 12
  • 10
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF), ELISA, Immunocytochemistry (ICC)
  • Binding Specificity

    • 58
    • 16
    • 8
    • 5
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 178-301

    Purpose

    Anti-SOX10 Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-SOX10 Antibody Picoband® (ABIN7600305). Tested in ELISA, IF, ICC, WB, Flow Cytometry applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human SOX10 recombinant protein (Position: R178-L301).

    Isotype

    IgG
  • Application Notes

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Bondurand N, Kuhlbrodt K, Pingault V, Enderich J, Sajus M, Tommerup N, Warburg M, Hennekam RC, Read AP, Wegner M, Goossens M (Sep 1999). "A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies". Human Molecular Genetics. 8 (9): 1785-9. 2. Huber WE, Price ER, Widlund HR, Du J, Davis IJ, Wegner M, Fisher DE (Nov 2003). "A tissue-restricted cAMP transcriptional response: SOX10 modulates alpha-melanocyte-stimulating hormone-triggered expression of microphthalmia-associated transcription factor in melanocytes". The Journal of Biological Chemistry.278 (46): 45224-30.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

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

    Alternative Name

    SOX10

    Background

    Synonyms: Transcription factor SOX-10, SOX10

    Tissue Specificity: Expressed in fetal brain and in adult brain, heart, small intestine and colon.

    Background: Transcription factor SOX-10 is a protein that in humans is encoded by the SOX10 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 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.

    Molecular Weight

    60-65 kDa

    Gene ID

    6663

    UniProt

    P56693

    Pathways

    Chromatin Binding
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