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AB5727 Anti-Sox10 Antibody

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AB5727
100 µg  
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      Replacement Information

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      Tableau de caractéristiques principal

      Species ReactivityKey ApplicationsHostFormatAntibody Type
      MWBRbAffinity PurifiedPolyclonal Antibody
      Description
      Catalogue NumberAB5727
      ReplacesAB5774
      Brand Family Chemicon®
      Trade Name
      • Chemicon
      DescriptionAnti-Sox10 Antibody
      Background InformationSox 10 is part of a 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. Sox 10 is expressed in multipotent neural crest stem cells, and its expression is downregulated upon their differentiation. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease.
      References
      Product Information
      FormatAffinity Purified
      HS Code3002 15 90
      PresentationAffinity purified immunoglobulin. Liquid.
      Quality LevelMQ100
      Applications
      ApplicationAnti-Sox10 Antibody detects level of Sox10 & has been published & validated for use in WB.
      Key Applications
      • Western Blotting
      Application NotesWestern blot: 0.1-0.5 μg/mL using ECL on fetal mouse brain tissue lysate. The antibody reacts with proteins of ~60 kDa. An additional band of ~120 kDa may also be seen depending on sample used.

      Optimal working dilutions must be determined by the end user.
      Biological Information
      ImmunogenSynthetic peptide from Sox10.
      HostRabbit
      SpecificitySox10. The immunogen sequence is 70% conserved with Sox8 and Sox9 and therefore the antibody may show cross reactivity to these proteins.
      Species Reactivity
      • Mouse
      Antibody TypePolyclonal Antibody
      Entrez Gene Number
      Entrez Gene SummaryThis 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.
      Gene Symbol
      • SOX10
      • OTTHUMP00000028515
      • WS4
      • DOM
      • WS2E
      • MGC15649
      UniProt Number
      UniProt SummaryFUNCTION: SwissProt: P56693 # Transcription factor that seems to function synergistically with the POU domain protein TST-1/OCT6/SCIP. Could confer cell specificity to the function of other transcription factors in developing and mature glia (By similarity).
      SIZE: 466 amino acids; 49911 Da
      SUBCELLULAR LOCATION: Cytoplasm. Nucleus.
      TISSUE SPECIFICITY: Expressed in fetal brain and in adult brain, heart, small intestine and colon.
      DISEASE: SwissProt: P56693 # Defects in SOX10 are a cause of Waardenburg syndrome type IV (WS4) [MIM:277580]; also known as Waardenburg-Shah syndrome. WS4 is characterized by the association of Waardenburg features (depigmentation and deafness) and the absence of enteric ganglia in the distal part of the intestine (Hirschsprung disease). & Defects in SOX10 are a cause of Yemenite deaf-blind hypopigmentation syndrome [MIM:601706]. The disorder consists of cutaneous hypopigmented and hyperpigmented spots and patches, microcornea, coloboma and severe hearing loss. Another case observed in a girl with similar skin symptoms and hearing loss but without microcornea or coloboma is reported as a mild form of this syndrome. & Defects in SOX10 are the cause of peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease (PCWH) [MIM:609136]; also called neurologic variant of Waardenburg-Shah syndrome. PCWH is a rare, complex and more severe neurocristopathy that includes features of 4 distinct syndromes: peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease.
      SIMILARITY: SwissProt: P56693 ## Contains 1 HMG box DNA-binding domain.
      Molecular WeightApprox. 55 kDa
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Usage Statement
      • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
      Storage and Shipping Information
      Storage ConditionsMaintain at +2-8°C in undiluted aliquots for up to 6 months after date of receipt.
      Packaging Information
      Material Size100 µg
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Référence GTIN
      AB5727 04053252401015

      Documentation

      Anti-Sox10 Antibody FDS

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      Anti-Sox10 Antibody Certificats d'analyse

      TitreNuméro de lot
      Anti-Sox 10 - 2154069 2154069
      Anti-Sox 10 - 2373396 2373396
      Anti-Sox 10 - 2446933 2446933
      Anti-Sox 10 - 1973216 1973216
      Anti-Sox 10 - 2049223 2049223
      Anti-Sox 10 - 3261328 3261328
      Anti-Sox 10 - 3460332 3460332
      Anti-Sox 10 - 3946454 3946454
      Anti-Sox 10 - 4019796 4019796
      Anti-Sox 10 - 4045793 4045793

      Références bibliographiques

      Aperçu de la référence bibliographiqueEspèceNº PubMed
      Myelin gene regulatory factor is required for maintenance of myelin and mature oligodendrocyte identity in the adult CNS.
      Koenning, M; Jackson, S; Hay, CM; Faux, C; Kilpatrick, TJ; Willingham, M; Emery, B
      The Journal of neuroscience : the official journal of the Society for Neuroscience  32  12528-42  2011

      Afficher le résumé
      22956843 22956843
      Human embryonic stem cell-derived oligodendrocyte progenitor cell transplants remyelinate and restore locomotion after spinal cord injury.
      Keirstead, Hans S, et al.
      J. Neurosci., 25: 4694-705 (2005)  2004

      Human15888645 15888645
      Meteorin: a secreted protein that regulates glial cell differentiation and promotes axonal extension
      Nishino, J. et al.
      EMBO J. , 23(9):1998-2008 (2004)  2004

      15085178 15085178

      Informations techniques

      Titre
      Derivation of oligodendrocyte progenitor cells from a human neural stem cell line

      Newsletters / Publications

      Title
      Cellutions - The newsletter for Cell Biology Researchers Volume 3: 2011

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      Catégories

      Life Science Research > Antibodies and Assays > Primary Antibodies