SOX5 Antibody

說明書

中文名稱：

SOX5兔多克隆抗體
貨號：

CSB-PA022432GA01HU
規(guī)格：

￥3,900
其他：

產(chǎn)品詳情
產(chǎn)品評價
相關(guān)產(chǎn)品
靶點詳情

產(chǎn)品詳情

Uniprot No.：

P35711
基因名：

SOX5
別名：

L SOX5 antibody; MGC35153 antibody; Sex determining region Y box 5 antibody; SOX 5 antibody; SOX 5 protein antibody; Sox5 antibody; SOX5 protein antibody; SOX5_HUMAN antibody; SRY (sex determining region Y) box 5 antibody; SRY box 5 antibody; Transcription factor SOX 5 antibody; Transcription factor SOX-5 antibody; Transcription factor SOX5 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human,Mouse,Rat
免疫原：

Human SOX5
免疫原種屬：

Homo sapiens (Human)
抗體亞型：

IgG
純化方式：

Antigen Affinity Purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
產(chǎn)品提供形式：

Liquid
應(yīng)用范圍：

ELISA,WB
Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評價

靶點詳情

功能：

Transcription factor involved in chondrocytes differentiation and cartilage formation. Specifically binds the 5'-AACAAT-3' DNA motif present in enhancers and super-enhancers and promotes expression of genes important for chondrogenesis, including cartilage matrix protein-coding genes, such as COL2A1 and AGC1. Required for overt chondrogenesis when condensed prechondrocytes differentiate into early stage chondrocytes: SOX5 and SOX6 cooperatively bind with SOX9 on active enhancers and super-enhancers associated with cartilage-specific genes, and thereby potentiate SOX9's ability to transactivate. Not involved in precartilaginous condensation, the first step in chondrogenesis, during which skeletal progenitors differentiate into prechondrocytes. Together with SOX6, required to form and maintain a pool of highly proliferating chondroblasts between epiphyses and metaphyses, to form columnar chondroblasts, delay chondrocyte prehypertrophy but promote hypertrophy, and to delay terminal differentiation of chondrocytes on contact with ossification fronts. Binds to the proximal promoter region of the myelin protein MPZ gene.
基因功能參考文獻：
1. Sox5 is a previously unrecognized regulator of beta-cell gene expression and secretory function PMID: 28585545
2. SOX5 overexpression increased Kruppel-like factor 4 (KLF4) gene expression, which was decreased by SOX5 silencing. KLF4 knockdown abrogated the suppressive effect of SOX5 overexpression on osteogenic differentiation of hMSCs. PMID: 29890823
3. Results show that SOX5 expression levels is increased in the synovium of patients with rheumatoid arthritis (RA). Its overexpression regulates the expression of RANKL in RA synovial fibroblasts. PMID: 27550416
4. SOX5, candidate gene, associated with clinical features of Depression (e.g., earlier age at onset and recurrent and more severe forms of Depression). Gene expression patterns in the prefrontal and anterior cingulate cortex most closely matched the genetic findings. PMID: 28969442
5. SOX5 promoted epithelial-mesenchymal transition (EMT) by regulation of Snail. PMID: 28365963
6. Short-SOX5 regulates transcription of human SPAG16L gene via directly binding to the promoter of SPAG16L. PMID: 28137312
7. results suggest that lnc-Sox5, which was stabilized by HuR, could regulate carcinogenesis of tongue cancer and may serve as a predicted target for tongue carcinoma therapies PMID: 28371600
8. 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. PMID: 28186563
9. The results of the present study suggest a role for SOX5 in the molecular pathogenesis of FL. PMID: 26115875
10. SOX5 has a strong inhibitory effect on MITF expression and seems to have a decisive clinical impact on melanoma during tumor progression. PMID: 26927636
11. Our results indicate for the first time that SOX5 is a novel regulator of epithelial-mesenchymal transition in hepatocellular carcinoma PMID: 25572815
12. Sox5-PAX5 fusion transcript is associated with B-cell precursor acute lymphoblastic leukemia. PMID: 25304615
13. These findings describe for the first time a functional role of SOX5 during late B cell development reducing the proliferative capacity and thus potentially affecting the differentiation of B cells. PMID: 24945754
14. High Sox5 expression is associated with pituitary tumor. PMID: 25305447
15. detection of SOX5 polymorphism in nonobstructive azoospermia contributing to predicting males at high risk of disease in Han Chinese population PMID: 24648396
16. Sox5 and Sox9 cause a significant increase in transactivation of the Catsper1 promoter. PMID: 25101494
17. 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. PMID: 24945754
18. depletion of Sox5 in breast cancer cells caused a dramatic decrease in Twist1 and chromosome immunoprecipitation assay showed that Sox5 can bind directly to the Twist1 promoter, suggesting that Sox5 transactivates Twist1 expression PMID: 24607904
19. Sox5 regulates the proliferation of malignant B cells. PMID: 24418753
20. Two cases of 12p12.1 deletion involving SOX5 present with dysmorphic features and developmental delay. PMID: 23498568
21. Our findings indicate that haploinsufficiency of SOX5 is a cause of intellectual disability without any striking physical anomalies. PMID: 23220431
22. L-Sox5 and Sox6 proteins enhance chondrogenic miR-140 microRNA expression by strengthening dimeric Sox9 activity PMID: 22547066
23. MiR-194 regulates chondrogenic differentiation of adipose-derived stem cells by targeting Sox5 PMID: 22396742
24. Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features PMID: 22290657
25. SOX trio gene and protein decreased with advancement of osteoarthritis in human articular cartilage. PMID: 21728837
26. Genetic variation in the transcription factor SOX5 is associated with COPD susceptibility PMID: 21330457
27. identified SOX5 and SOX6 as the first two SHOX-interacting proteins and have shown that this interaction regulates aggrecan expression, an essential factor in chondrogenesis and skeletal development. PMID: 21262861
28. SPAG6 is a S-SOX5 target gene, indicating a key role for S-SOX5 in the formation and function of motile cilia. PMID: 20668334
29. Observational study, meta-analysis, and genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 20639392
30. Clinical trial and genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 20195266
31. DAD-R, SOX5, and EKI1 map within region of chromosome 12p whose duplication is related to reduced apoptosis in human testicular seminomas. PMID: 11912161
32. SOX5 is aberrantly expressed in glioma PMID: 17230535
33. SOX5 is upregulated by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma PMID: 17554380
34. studies of SOX5 in cell lines, xenografts and human prostate specimens, at both the RNA and protein levels, found overexpression of the gene in tumors. This overexpression was then subsequently found by FISH to be caused by amplification of the region PMID: 19173284
35. Sox5 may suppress the oncogenic effects of PDGFB signaling during glioma development by regulating p27(Kip1) in a p19(Arf)-dependent manner, leading to acute cellular senescence. PMID: 19219070
36. Meta-analysis and genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 20062060
37. Clinical trial and genome-wide association study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) PMID: 18519826
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相關(guān)疾病：

Lamb-Shaffer syndrome (LAMSHF)
亞細胞定位：

Nucleus.
數(shù)據(jù)庫鏈接：

HGNC: 11201

OMIM: 604975

KEGG: hsa:6660

STRING: 9606.ENSP00000398273

UniGene: Hs.434948

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