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SOX5 encodes 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. Additionally we are shipping SOX5 Antibodies (44) and SOX5 Proteins (5) and many more products for this protein.
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SOX5 promoted epithelial-mesenchymal transition (EMT (show ITK ELISA Kits)) by regulation of Snail (show SNAI1 ELISA Kits).
Short-SOX5 regulates transcription of human SPAG16L gene via directly binding to the promoter of SPAG16L.
results suggest that lnc-Sox5, which was stabilized by HuR (show ELAVL1 ELISA Kits), could regulate carcinogenesis of tongue cancer and may serve as a predicted target for tongue carcinoma therapies
Collectively, these findings indicate that SOX5 is a novel candidate gene for Alzheimer's disease(AD) with an important role in neuronal function. The genetic findings warrant further studies to identify and characterize SOX5 variants that confer risk for AD, amyotrophic lateral sclerosis and intellectual disability.
The results of the present study suggest a role for SOX5 in the molecular pathogenesis of FL.
SOX5 has a strong inhibitory effect on MITF (show MITF ELISA Kits) expression and seems to have a decisive clinical impact on melanoma during tumor progression.
Our results indicate for the first time that SOX5 is a novel regulator of epithelial-mesenchymal transition in hepatocellular carcinoma
Sox5-PAX5 (show PAX5 ELISA Kits) fusion transcript is associated with B-cell precursor acute lymphoblastic leukemia.
Identified two new splice variants of SOX5 in human B cells, encoding the known L-SOX5B isoform and a new shorter isoform L-SOX5F. SOX5 limits the proliferative capacity of human primary B lymphocytes and potentially affects the differentiation of human B cells during the germinal center responses.
High Sox5 expression is associated with pituitary tumor.
These results demonstrate that C/T missense mutation within the SOX5 gene is involved in bull sperm quality.
show that Sox5 is essential for activation of BMP target genes in embryos and explants, that it physically interacts with BMP R-Smads
Study revealed that Sox5 and Sox6 prevent oligodendroglial differentiation, thus ensuring that the progenitor cells first reach their proper destination and only then lose their migratory capacity
This study demonstrated that Sox13 functionally complements the related Sox5 and Sox6 as important developmental modulators in mouse spinal cord oligodendrocytes.
Results show that Sox9 (show SOX9 ELISA Kits), Sox5, and Sox13 (show SOX13 ELISA Kits) transcription factors are expressed in postnatal testis and may regulate multiple functions such as steroidogenesis and spermatogenesis.
Results suggest that L-Sox5 protein expression may diminish along with the progress of chondrogenic differentiation. L-Sox5 may act as a negative regulator if expressed aberrantly at least in part by regulating the critical fate of chondrogenesis.
T cell-specific Sox5-deficient mice exhibit impaired Th17 cell differentiation and are resistant to experimental autoimmune encephalomyelitis and delayed-type hypersensitivity.
Sox5 regulates the proliferation of malignant B cells.
L-Sox5 and Sox6 proteins enhance chondrogenic miR (show MLXIP ELISA Kits)-140 microRNA expression by strengthening dimeric Sox9 (show SOX9 ELISA Kits) activity
MiR (show MLXIP ELISA Kits)-194 regulates chondrogenic differentiation of adipose-derived stem cells by targeting Sox5
Genetic variation in the transcription factor SOX5 is associated with COPD (show ARCN1 ELISA Kits) susceptibility
SPAG6 (show SPAG6 ELISA Kits) is a S-SOX5 target gene, indicating a key role for S-SOX5 in the formation and function of motile cilia.
This gene encodes 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. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The encoded protein may play a role in chondrogenesis. A pseudogene of this gene is located on chromosome 8. Multiple transcript variants encoding distinct isoforms have been identified for this gene.
transcription factor SOX-5
, SRY (sex determining region Y)-box 5
, Transcription factor Sox-5
, transcription factor LSox5-I
, SRY-box containing gene 5
, SRY-box containing gene 5-like 1
, SRY-box 5