
Thermo Fisher Scientific SOX2 (Embryonic Stem Cell Marker) Recombinant Rabbit Monoclonal Antibody (SOX2/4267R)
SOX2 단백질을 표적으로 하는 재조합 토끼 단일클론 항체로, 배아줄기세포 마커 연구에 적합함. 인간 시료 반응성이 있으며, 핵 내 SOX2 발현 검출에 사용. Protein A/G 정제, 200 µg/mL 농도, 4°C 보관. 연구용으로만 사용 가능.
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Thermo Fisher Scientific SOX2 (Embryonic Stem Cell Marker) Recombinant Rabbit Monoclonal Antibody (SOX2/4267R)
Applications and Tested Dilution
- Immunohistochemistry (Paraffin) (IHC (P)): 1–2 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | SOX2/4267R |
| Immunogen | Recombinant fragment of human SOX2 protein (amino acids 1–50) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 200 µg/mL |
| Purification | Protein A/G |
| Storage Buffer | PBS with 0.05% BSA |
| Contains | 0.05% sodium azide |
| Storage Conditions | 4°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
- Antibody stability: 24 months
- Positive Control: MCF-7 cells, human lung or cervical carcinoma
- Cellular Localization: Nucleus
Specificity Comments:
SOX2 is required for stem cell maintenance in the central nervous system and regulates gene expression in the stomach. It stabilizes embryonic stem cells in a pluripotent state by maintaining Oct 3/4 expression levels. SOX2 is associated with aggressive phenotypes of various cancers, including breast, head and neck, gastric, colorectal, bladder, and small cell lung cancers. It is expressed in a high percentage of lung squamous cell carcinomas and is an independent favorable prognostic marker.
Target Information
SOX2 is an intronless gene encoding a member of the SRY-related HMG-box (SOX) family of transcription factors involved in embryonic development and cell fate determination. The SOX2 protein is essential for stem-cell maintenance in the central nervous system and regulates gene expression in the stomach. The gene lies within an intron of SOX2 overlapping transcript (SOX2OT). SOX2 may act as a transcriptional activator in complex with other proteins. Mutations in SOX2 are associated with bilateral anophthalmia, optic nerve hypoplasia, and syndromic microphthalmia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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