SOX10 Monoclonal Antibody (1-11), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA544626-Each-of-1 | In Stock | ₹ 42,720.00 |
PIMA544626 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 42,720.00
GST (18%): ₹ 7,689.60
Total Price: ₹ 50,409.60
Antigen
SOX10
Classification
Monoclonal
Concentration
2 mg/mL
Formulation
PBS with 0.2% BSA, 40% glycerol and 0.05% sodium azide; pH 7.4
Gene Accession No.
Q04888
Gene Symbols
SOX10
Immunogen
Recombinant protein within human SOX10 aa 80-310.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Mouse
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Clone
1-11
Conjugate
Unconjugated
Gene
SOX10
Gene Alias
cls; cls/sox10; colorless; colourless; colourless/sox10; DOM; dominant megacolon; dominant megacolon, mouse, human homolog of; golas; gos; HMG-box transcription factor Sox10; MGC15649; PCWH; Protein SOX-21; SOX10; Sox-10; sox10 protein; sox10b; Sox21; SOX9; SRY; SRY (sex determining region Y)-box 10; SRY (sex determining region Y)-box 9 (campomelic dysplasia, autosomal sex-reversal); SRY box 10; SRY-box 10; SRY-box containing gene 10; SRY-box containing protein 10; SRY-box transcription factor 10; SRY-related HMG-box gene 10; transcription factor SOX-10; Transcription factor SOX-M; WS2E; WS4; WS4C; zgc:100757
Host Species
Mouse
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
20665
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Isotype
IgG1
Related Products
Description
- 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.