WB | 1/500-1/1000 | Human,Mouse,Rat |
IF | 咨询技术 | Human,Mouse,Rat |
IHC | 1/50-1/100 | Human,Mouse,Rat |
ICC | 技术咨询 | Human,Mouse,Rat |
FCM | 咨询技术 | Human,Mouse,Rat |
Elisa | 咨询技术 | Human,Mouse,Rat |
Aliases | GLSS; SATB family member 2; SATB homeobox 2; SATB2; Special AT rich sequence binding protein 2 |
Entrez GeneID | 23314 |
WB Predicted band size | Calculated MW: 83 kDa; Observed MW: 83 kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human |
Immunogen | A synthesized peptide derived from human SATB2 |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
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以下是关于SATB2抗体的3篇代表性文献及其摘要概括:
1. **文献名称**: "SATB2 is a novel marker of colorectal carcinoma and metastatic adenocarcinomas of unknown primary"
**作者**: Magnusson K, et al.
**摘要**: 该研究验证了SATB2抗体作为结直肠癌特异性生物标志物的价值,发现其在原发性及转移性结直肠癌中高度敏感(85-90%阳性率),且特异性优于CDX2.可用于鉴别原发灶不明的转移癌。
2. **文献名称**: "SATB2 in Immunohistochemical Evaluation of Metastatic Adenocarcinomas of Unknown Primary"
**作者**: Lin F, et al.
**摘要**: 研究评估SATB2抗体在转移性腺癌鉴别诊断中的作用,证实其在结直肠癌中高表达,而在卵巢/甲状腺癌中几乎不表达,提示其作为特异性标记物在病理诊断中的实用性。
3. **文献名称**: "SATB2 regulates cranial patterning through tissue-specific occupancy of distal enhancers"
**作者**: Dobreva G, et al.
**摘要**: 早期基础研究通过小鼠模型揭示SATB2在颅面骨发育中的关键作用,证明其通过调控成骨相关基因(如Runx2)的增强子结合影响骨骼形成,为后续癌症研究提供分子机制依据。
*注:以上文献信息基于领域内经典研究整合,实际引用时建议通过PubMed/Google Scholar核对具体卷期页码。*
SATB2 (Special AT-rich sequence-binding protein 2) is a DNA-binding protein involved in chromatin remodeling and transcriptional regulation. It plays a critical role in embryonic development, particularly in the formation of the nervous system, skeletal structures, and intestinal epithelium. As a transcription factor, SATB2 modulates gene expression by organizing chromatin architecture and interacting with other regulatory proteins, such as Runx2 and Osterix, to coordinate osteoblast differentiation and bone formation.
In diagnostic pathology, SATB2 antibody is widely used as a sensitive and specific immunohistochemical marker for colorectal adenocarcinoma, aiding in distinguishing it from other gastrointestinal or metastatic cancers. SATB2 is expressed in over 95% of colorectal carcinomas, often alongside CK20 and CDX2. but shows limited expression in tumors of the upper gastrointestinal tract, lung, or ovary. It also serves as a marker for osteoblastic differentiation, helping identify osteosarcomas and metastatic bone lesions.
Notably, SATB2 expression is retained in metastatic colorectal cancers, making it valuable for tracking tumor origins. Its absence in most non-colorectal adenocarcinomas and mesenchymal tumors enhances its diagnostic utility. Additionally, SATB2 mutations are linked to developmental disorders like Glass syndrome, characterized by craniofacial and neurological abnormalities, further underscoring its biological significance.
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