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AB5727 Anti-Sox10 Antibody

AB5727
100 µg  
Purchase on Sigma-Aldrich

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Tabela kluczowych gatunków

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
Numer katalogowy GTIN
AB5727 04053252401015

Documentation

Anti-Sox10 Antibody MSDS

Title

Safety Data Sheet (SDS) 

Anti-Sox10 Antibody Certificates of Analysis

TitleLot Number
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

References

Reference overviewSpeciesPub Med ID
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

Pokaż streszczenie
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

Technical Info

Title
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