SRY (Sex Determining Region Y)-Box 2 (SOX2) antibody
| Antigen | SRY (Sex Determining Region Y)-Box 2 (SOX2) |
| Synonyms | ANOP3, MCOPS3, MGC2413, RGD1565646, SOX2, MGC148683, lcc, ysb, Sox-2 |
| Clonality | Monoclonal (57CT23-3-4) |
| Host |
Alternatives Mouse |
| Reactivity |
Alternatives Human |
| Conjugate |
Alternatives Un-conjugated |
| Application |
Alternatives Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS), ELISA |
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5 references available |
| Certificates | ISO 9001:2008 |
| Catalog no. | ABIN387799 |
| Quantity | 50 ul mg (Ascites) (Variants) |
| Price | 280.50 $ Plus shipping costs $45.00 |
| Shipping to |
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| Availability | Will be delivered in 2 to 3 Business Days |
Additional Information
| Alternative name | SOX2 |
| Gene ID | 6657 |
| UniProt | P48431 |
| Immunogen | Human SOX2 recombinant protein is used to produce this monoclonal antibody. |
| Isotype | IgG1 |
| Clone | 57CT23-3-4 |
| Description | Other names: Transcription factor SOX-2 |
| Characteristics | Mouse Monoclonal Antibody (Mab) |
| Specificity | Human SOX2 recombinant protein is used to produce this monoclonal antibody. |
| Molecular Weight | 34310 DA |
| Comments |
Background: This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). |
Application Details
| Application Notes | The suggested dilution is: ELISA ~~ 1:10000 Western blotting~~ 1:200~2000 Immunohistochemistry ~~ 1:50~100 Flow cytometric~~1:50~100 |
| Concentration | Ascites |
| Buffer | Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide. |
| Storage | Maintain refrigerated at 2-8 deg C for up to 6 months. For long term storage store at -20 deg C in small aliquots to prevent freeze-thaw cycles |
| Research Area | Stem Cells, Transcription Factors, Signaling |
| Restrictions | For Research Use only |
Images
Publications
| Product |
Reis, Tyler, Schneider et al.: "Examination of SOX2 in variable ocular conditions identifies a recurrent deletion in microphthalmia and lack of mutations in other phenotypes." in: Molecular vision, Vol. 16, pp. 768-73, 2010 (PubMed).
Gonzalez-Rodriguez, Pelcastre, Tovilla-Canales et al.: "Mutational screening of CHX10, GDF6, OTX2, RAX and SOX2 genes in 50 unrelated microphthalmia-anophthalmia-coloboma (MAC) spectrum cases." in: The British journal of ophthalmology, Vol. 94, Issue 8, pp. 1100-4, 2010 (PubMed). Ge, Zhou, Chen et al.: "Sox2 is translationally activated by eukaryotic initiation factor 4E in human glioma-initiating cells." in: Biochemical and biophysical research communications, Vol. 397, Issue 4, pp. 711-7, 2010 (PubMed). Sholl, Barletta, Yeap et al.: "Sox2 protein expression is an independent poor prognostic indicator in stage I lung adenocarcinoma." in: The American journal of surgical pathology, Vol. 34, Issue 8, pp. 1193-8, 2010 (PubMed). Zhang, Efendic, Brismar et al.: "Effects of MCF2L2, ADIPOQ and SOX2 genetic polymorphisms on the development of nephropathy in type 1 Diabetes Mellitus." in: BMC medical genetics, Vol. 11, pp. 116, 2010 (PubMed). |
Alternatives
Alternatives for antigen "SRY (Sex Determining Region Y)-Box 2 (SOX2)", type "Antibodies"




Alternatives