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Human Polyclonal SNAI1 Primary Antibody for IF, IHC (p) - ABIN498268
Feng, Di, Tao, Chang, Lu, Fan, Shan, Li, Yang: PDK1 regulates vascular remodeling and promotes epithelial-mesenchymal transition in cardiac development. in Molecular and cellular biology 2010
Show all 5 Pubmed References
Human Polyclonal SNAI1 Primary Antibody for FACS, ICC - ABIN4899437
Satelli, Mitra, Brownlee, Xia, Bellister, Overman, Kopetz, Ellis, Meng, Li: Epithelial-mesenchymal transitioned circulating tumor cells capture for detecting tumor progression. in Clinical cancer research : an official journal of the American Association for Cancer Research 2015
Show all 3 Pubmed References
Guinea Pig Polyclonal SNAI1 Primary Antibody for IHC, WB - ABIN2777858
Zhou, Deng, Xia, Xu, Li, Gunduz, Hung: Dual regulation of Snail by GSK-3beta-mediated phosphorylation in control of epithelial-mesenchymal transition. in Nature cell biology 2004
Show all 4 Pubmed References
Human Monoclonal SNAI1 Primary Antibody for ELISA, WB - ABIN969409
Wanami, Chen, Peiró, García de Herreros, Bachelder: Vascular endothelial growth factor-A stimulates Snail expression in breast tumor cells: implications for tumor progression. in Experimental cell research 2008
Show all 2 Pubmed References
Human Polyclonal SNAI1 Primary Antibody for ELISA, ICC - ABIN6265200
Li, Shen, Wang, Li, Wang, Jiang, Zhou, Feng: EGCG regulates the cross-talk between JWA and topoisomerase IIα in non-small-cell lung cancer (NSCLC) cells. in Scientific reports 2016
Show all 2 Pubmed References
Human Monoclonal SNAI1 Primary Antibody for IHC, WB - ABIN2668578
Rosivatz, Becker, Kremmer, Schott, Blechschmidt, Höfler, Sarbia: Expression and nuclear localization of Snail, an E-cadherin repressor, in adenocarcinomas of the upper gastrointestinal tract. in Virchows Archiv : an international journal of pathology 2006
Show all 2 Pubmed References
Human Monoclonal SNAI1 Primary Antibody for IF, ELISA - ABIN520326
Rath, Miller, Litofsky, Anthony, Feng, Franklin, Pei, Free, Liu, Ren, Kirk, Shi: Isolation and characterization of a population of stem-like progenitor cells from an atypical meningioma. in Experimental and molecular pathology 2011
Human Polyclonal SNAI1 Primary Antibody for WB - ABIN388812
Barbu, Zhang, Berenstein, Groves, Parks, Siraganian: The transcription factor Zeb2 regulates signaling in mast cells. in Journal of immunology (Baltimore, Md. : 1950) 2012
Human Monoclonal SNAI1 Primary Antibody for ELISA, WB - ABIN967055
Herranz, Pasini, Díaz, Francí, Gutierrez, Dave, Escrivà, Hernandez-Muñoz, Di Croce, Helin, García de Herreros, Peiró: Polycomb complex 2 is required for E-cadherin repression by the Snail1 transcription factor. in Molecular and cellular biology 2008
Show all 2 Pubmed References
Human Monoclonal SNAI1 Primary Antibody for IHC, WB - ABIN2732276
Qin, He, Tang, Ye, Dang, Lu, Wang, Li, Yan, Ma: MicroRNAs Provide Feedback Regulation of Epithelial-Mesenchymal Transition Induced by Growth Factors. in Journal of cellular physiology 2015
The authors identify SNAI1 as the key Epithelial-Mesenchymal Transition transcriptional factor required for the specification of definitive endoderm.
Snail functions as a metabolic switch between aerobic glycolysis and pentose phosphate pathway by repressing PFKP, a cancer-specific PFK-1, allowing cancer cell survival under metabolic stress.
At the molecular level, transcription of the adherens junction protein E (show CRISP1 Antibodies)-cadherin (show CDH1 Antibodies) is upregulated on nicotinic acid addition, leading to accumulation of E-cadherin (show CDH1 Antibodies) protein at the cell-cell boundary. This can be attributed to nicotinic acid's ability to facilitate the ubiquitination and degradation of Snail1, a transcription factor that represses E-cadherin (show CDH1 Antibodies) expression.
Dub3 (show USP17L2 Antibodies) is identified as a bona fide Snail1 deubiquitinase, which interacts with and stabilizes Snail1.
High SNAIL1 expression is associated with breast invasive ductal carcinoma.
The present study illustrated that downregulation of CDK10 (show CDK10 Antibodies) expression activated Snaildriven EMT (show ITK Antibodies) and consequently promoted glioma metastasis, suggesting that CDK10 (show CDK10 Antibodies) may serve as a potential molecular target for glioma therapy.
Binding of HIV1 Tat (show TAT Antibodies) to TIP30 (show HTATIP2 Antibodies) enhanced epithelial-to-mesenchymal transition and metastasis by regulating the nuclear translocation of Snail.
Chronic hypoxia-induced slug promotes invasive behavior of prostate cancer cells by activating the expression of ephrin-B1 (show EFNB1 Antibodies).
FBXW7 (show FBXW7 Antibodies) conduction of tumour suppression was partly through degrading Snai1 directly for ubiquitylating regulation in NSCLC.
It is concluded that epithelial-mesenchymal transition is involved in human diabetic cataract, and upregulation of miR (show MLXIP Antibodies)-30a can repress epithelial-mesenchymal transition through its targeting of SNAI1 in lens epithelial cells, which make miR (show MLXIP Antibodies)-30a a novel target of therapeutic intervention for human diabetic cataract.
CDK4 (show CDK4 Antibodies)/CDK6 (show CDK6 Antibodies)-dependent activation of DUB3 (show USP17L2 Antibodies) regulates cancer metastasis through SNAIL1.
Neutrophils and Snail orchestrate the establishment of a pro-tumor microenvironment in lung cancer.
Nrf2 (show NFE2L2 Antibodies) attenuates Epithelial-mesenchymal transition and fibrosis process by regulating the expression of snail in pulmonary fibrosis.
Pbx-dependent Epithelial-mesenchymal transition programs mediate murine upper lip/primary palate morphogenesis and fusion via regulation of Snail1.
a Snail1-ATGL (show PNPLA2 Antibodies) axis that regulates adipose lipolysis and fatty acid release, is reported.
A20 (show TNFAIP3 Antibodies) promotes metastasis of aggressive basal-like breast cancers through multi-monoubiquitylation of Snail1.
Metagenomic analysis revealed direct correlation between PPARGC1A, SNAI1, and metastatic lung disease.
both Snail and Slug are able to form binary complexes with either YAP (show YAP1 Antibodies) or TAZ (show TAZ Antibodies) that, together, control YAP (show YAP1 Antibodies)/TAZ (show TAZ Antibodies) transcriptional activity and function throughout mouse development.
results demonstrate that skeletal stem/stromal cell mobilize Snail/Slug-YAP (show YAP1 Antibodies)/TAZ (show TAZ Antibodies) complexes to control stem cell function
these results might suggest that calcineurin inhibitor (show RCAN1 Antibodies)-induced tubular SNAI1 protein cytoplasmic accumulation, possibly because of impaired SNAI1 proteasomal degradation and nuclear translocation, might be a sign of a diseased profibrotic epithelial phenotype.
While either Snail or Serpent induced a profound loss of epithelial polarity and tissue organisation, Serpent but not Snail also induced an increase in the size of wing discs. Furthermore, the Serpent-induced tumour-like tissues were able to grow extensively when transplanted into the abdomen of adult hosts.
Disruption of Snail expression in follicle stem cells compromises proliferation, but not maintenance. FSCs with excessive Snail expression had increased proliferation and lifespan, accompanied by a moderate decrease inE-cadherin expression (required for adhesion of FSCs to their niche) at the junction between their adjacent cells, indicating a conserved role of Snail in E-cadherin (show CDH1 Antibodies) inhibition.
during gastrulation of Drosophila embryos, Sna expression downregulates polarity protein Baz which in turn results in junction disassembly at protein levels.
evidence for mechanosensitivity of cell-cell junctions and implications that myosin-mediated tension can prevent Snail-driven Eepithelial-mesenchymal transitions
Snail can potentiate enhancer activation by collaborating with different activators, providing a new mechanism by which Snail regulates development.
Rapid transcription kinetics and negative autoregulation are responsible for the remarkable homogeneity of snail expression and the coordination of mesoderm invagination.
Study shows that Sna represses transcription of pbl in the mesoderm primordium of D. melanogaster via one or more Sna-binding sites, which are conserved among species of the Drosophila genus, but not in the mosquito, correlating with the different modes of gastrulation in the different genuses.
Complex interactions between cis (show CISH Antibodies)-regulatory modules in native conformation are critical for Drosophila snail expression.
The Snail repressor positions Notch (show NOTCH1 Antibodies) signaling in the Drosophila embryo.
results show that Sna has a positive regulatory function on sim (show SIM2 Antibodies) expression in the presumptive mesectoderm; this positive effect of Sna depends on the Su(H (show RBPJ Antibodies))-binding sites within the sim (show SIM2 Antibodies) promoter, suggesting that Sna regulates Notch (show NOTCH1 Antibodies) signaling
The transcription factor Snail1 is essential for tissue separation, enabling paraxial protocadherin (PAPC (show PCDH8 Antibodies)) to promote tissue separation through novel functions.
Interaction with Snail1/2, and Twist function more generally, is regulated by GSK-3-beta-mediated phosphorylation of conserved sites in the WR domain.
the same E3 ubiquitin ligase (show MUL1 Antibodies) known to regulate Snail family proteins, Partner of paired (Ppa (show FBXL14 Antibodies)), also controlled Twist stability and did so in a manner dependent on the Twist WR-rich domain
data support a Snail1-dependent mechanism of BBB (show ALMS1 Antibodies) disruption and penetration by meningeal pathogens.
Snail genes lie in regions of extensive paralogy, revealing their common origin through segmental or chromosomal duplication
data suggest that Nrz, in addition to its effect on apoptosis, contributes to cell movements during gastrulation by negatively regulating the expression of Snail-1, a transcription factor that controls cell adhesion
Snail genes not only act as inducers of epithelial-to-mesenchymal transition, but also as more general regulators of cell adhesion and movement.
NF-kappaB (show NFKB1 Antibodies) and Snail1a coordinate the cell cycle with gastrulation.
The Drosophila embryonic protein snail is a zinc finger transcriptional repressor which downregulates the expression of ectodermal genes within the mesoderm. The nuclear protein encoded by this gene is structurally similar to the Drosophila snail protein, and is also thought to be critical for mesoderm formation in the developing embryo. At least two variants of a similar processed pseudogene have been found on chromosome 2.
, protein snail homolog 1
, snail 1 homolog
, snail 1 zinc finger protein
, snail 1, zinc finger protein
, snail homolog 1
, zinc finger protein SNAI1
, snail like protein
, Protein snail-like protein 1
, snail homolog 1 (Drosophila)
, zinc-finger transcription factor Snail
, protein Xsnail
, protein snail homolog Sna
, protein xSna
, snail protein
, zinc finger protein with snail domain similar to escargot
, transcription factor protein
, snail zinc finger protein
, snail-like protein 1
, snail family zinc finger 1a