SOX10 Mouse anti-Human, Mouse, Rat, Clone: 20B7, eBioscience
Mouse Monoclonal Antibody
Manufacturer: Invitrogen 14592382
Description: The monoclonal antibody 20B7 recognizes Sox10, is a member of the Sox superfamily (SRY-related HMG-box) that contain a DNA binding domain (high-mobility group domain) and functions as a transcription factor. Initially, Sox10 expression is localized to the developing neural crest and peripheral nervous system, but later is expressed in glial progenitors and mature oligodendrocytes. Sox10 is involved in stem cell maintece, melanocyte differentiation, as well as central and peripheral gliogenesis and neurogenesis. Sox10 regulation of downstream proteins such as MASH1, PHOX2B, PDGF-alpha, and MITF is dependent on expression level. Sox10 is also expressed in multipotent vascular stem cells, melanomas, and gliomas. The 20B7 antibody is reported to recognize human and rat Sox 10, and based on homology should recognize mouse Sox10. Applications Reported: This 20B7 antibody has been reported for use in immunohistochemical staining of frozen tissue sections, immunohistochemical staining of formalin-fixed paraffin embedded tissue sections, microscopy, and immunocytochemistry. Applications Tested: This 20B7 antibody has been tested by immunocytochemistry of formaldehyde fixed and permeabilized rat cells. This 20B7 antibody has also been tested by immunohistochemistry of human formalin-fixed paraffin embedded tissue sections using low pH antigen retreival and can be used at less than or equal to 10 µg/mL for both applications.It is recommended that the antibody be carefully titrated for optimal performance in the assay of interest. Purity: Greater than 90%, as determined by SDS-PAGE. Aggregation: Less than 10%, as determined by HPLC. Filtration: 0.2 µm post-manufacturing filtered. SOX10 is 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. This protein may act as a transcriptional activator after forming a protein complex with other proteins. It 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.
|PBS with 0.09% sodium azide; pH 7.2|
|O55170, Q04888, P56693|
|SRY, sex determining region Y-box 10 , DOM, MGC15649, WS4, SRY-related HMG-box gene 10|
|Human, Mouse, Rat|
|Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Frozen), Immunohistochemistry (Paraffin)|
|20665, 29361, 6663|
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