SOX10 Protein (Myc-DYKDDDDK Tag)
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- Target See all SOX10 Proteins
- SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This SOX10 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human SOX10 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product SOX10 Protein
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))
- Alternative Name
- Sox10 (SOX10 Products)
- Synonyms
- DOM Protein, PCWH Protein, WS2E Protein, WS4 Protein, WS4C Protein, SOX-10 Protein, SOX10 Protein, dom Protein, ws4 Protein, Dom Protein, Sox21 Protein, SOX9 Protein, cls/sox10 Protein, zgc:100757 Protein, SRY-box 10 Protein, SRY box 10 Protein, SRY-box 10 L homeolog Protein, SRY (sex determining region Y)-box 10 Protein, SOX10 Protein, Sox10 Protein, sox10.L Protein, sox10 Protein
- 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.
- Molecular Weight
- 49.7 kDa
- NCBI Accession
- NP_008872
- Pathways
- Chromatin Binding
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