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Members of the SOX family of transcription factors are characterized by the presence of a DNA-binding high mobility group (HMG) domain, homologous to the HMG box of sex-determining region Y (SRY). Additionally we are shipping SOX12 Antibodies (54) and SOX12 Proteins (5) and many more products for this protein.
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SOX12 can increase the expression of CDK4 (show CDK4 ELISA Kits) and IGF2BP1 (show IGF2BP1 ELISA Kits), which confer malignant phenotypes to HepatocellularCarcinoma.
Data found that, in hepatocellular carcinoma (HCC) cell lines, Sox12+ HCC cells generated significantly more tumor spheres in culture, were more chemo-resistant to cisplatin, were detected in circulation more frequently, and formed distal tumor more frequently compared to Sox12- HCC cells. Moreover, Sox12 appeared to functionally contribute to the stemness of HCC cells.
SOX12 may be involved in leukemia progression by regulating the expression of beta-catenin (show CTNNB1 ELISA Kits) and then interfering with TCF (show HNF4A ELISA Kits)/Wnt (show WNT2 ELISA Kits) pathway, which may be a target for AML (show RUNX1 ELISA Kits).
In this study we screened the transcriptional profiles of 70 MCL patients for SOXC cluster and miR17, miR18a, miR19b and miR92a, from the miR-17-92 cluster. Gene expression analysis showed higher SOX11 and SOX12 levels compared to SOX4 (P = 0.0026). Moreover we found a negative correlation between the expression of SOX11 and SOX4
Up-regulated Sox12 induced by FoxQ1 (show FOXQ1 ELISA Kits) promotes hepatocellular carcinoma invasion and metastasis by transactivating Twist1 (show TWIST1 ELISA Kits) and FGFBP1 (show FGFBP1 ELISA Kits) expression.
This genome-wide screen has identified two novel metastatic suppressors: TMED3 and SOX12, the knockdown of which increases metastatic growth after direct seeding.
SOX12 and NRSN2 were identified as candidate genes that may be involved in the developmental defects in 20p13 microdeletion.
SOXC proteins act cell- and non-cell-autonomously in perichondrocytes and chondrocytes to establish noncanonical WNT (show WNT2 ELISA Kits) signaling crosstalk essential for growth plate induction and control
Study show that the survival of neural and mesenchymal progenitor cells critically relies on the redundantly acting SoxC transcription factors Sox4, Sox11 and Sox12.
Sox4 and Sox11 function redundantly with Sox12 and can compensate its loss during mouse development.
Members of the SOX family of transcription factors are characterized by the presence of a DNA-binding high mobility group (HMG) domain, homologous to the HMG box of sex-determining region Y (SRY). Forming a subgroup of the HMG domain superfamily, SOX proteins have been implicated in cell fate decisions in a diverse range of developmental processes. SOX transcription factors have diverse tissue-specific expression patterns during early development and have been proposed to act as target-specific transcription factors and/or as chromatin structure regulatory elements. The protein encoded by this gene was identified as a SOX family member based on conserved domains, and its expression in various tissues suggests a role in both differentiation and maintenance of several cell types.
, SRY-related HMG-box gene 22
, transcription factor SOX-12
, SRY-box containing gene 12
, Transcription factor Sox-33
, transcription factor Sox-12