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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
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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
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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 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
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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 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 IHC, WB - ABIN2452265
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
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 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
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
snail is required for Drosophila gastrulation and is not replaceable by Escargot or Worniu.
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 (show GSK3b Antibodies)-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
Study provides evidence that SNAI1 promotes renal cell carcinoma (show MOK Antibodies) migration and invasion. Its expression is regulated by miR (show MLXIP Antibodies)-211 which targets its 3'-UTR (show UTS2R Antibodies).
FLNA (show FLNA Antibodies) upregulation correlates with Snail-induced epithelial to mesenchymal transition in colorectal carcinoma.
Slug (show SNAI2 Antibodies) is a positive regulator, and Snail a negative regulator, of PLD2 (show PLD2 Antibodies) expression.
Metagenomic analysis revealed direct correlation between PPARGC1A (show PPARGC1A Antibodies), SNAI1, and metastatic lung disease.
Results indicate that HCV core induced epithelial-mesenchymal transition (EMT (show ITK Antibodies)) by interacting with the transcriptional repressor complex Snail/HDAC1 (show HDAC1 Antibodies)/2 at the E-cadherin (show CDH1 Antibodies) promoter, which led to E-cadherin (show CDH1 Antibodies) repression and increased invasiveness of hepatoma cells.
High SNAIL expression is associated with liver neoplasms.
Results demonstrated that over expression of Snail suppresses Cryptic expression and confirmed that Snail directly binds to Cryptic gene promoter and regulates its expression.
Data show that histone demethylase (show MBD2 Antibodies) JMJD3 (show Kdm6b Antibodies) was reduced and its target gene Snai1 expression was down-regulated after HOTAIR suppression.
This study demonstrates that hepatitis C virus NS4B protein induces epithelial to mesenchymal transition progression via the upregulation of Snail in hepatocellular carcinoma, which may be a novel underlying mechanism for hepatitis C virus-associated hepatocellular carcinoma development, invasion and metastasis.
The expression of the transcription factor Snail is strongly associated with longer disease-free and overall survival.
both Snail and Slug (show SNAI2 Antibodies) 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 (show SNAI2 Antibodies)-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.
Snail1 as a molecular bypass that suppresses the anti-proliferative and pro-apoptotic effects exerted by wild-type p53 (show TP53 Antibodies) in breast cancer
Snail1 deficiency modified the phenotype of pancreatic tumors .
miR (show MLXIP Antibodies)-200 promotes the mesenchymal to epithelial transition by suppressing multiple members of the Zeb2 (show ZEB2 Antibodies) and Snail1 transcriptional repressor complexes, such as Smad2 (show SMAD2 Antibodies) and Smad5 (show SMAD5 Antibodies).
show that Snail1-induced fibrosis can be reversed in vivo and that obstructive nephropathy can be therapeutically ameliorated in mice by targeting Snail1 expression
Results suggest that Snai1 is a key factor that triggers ESCs (show NR2E3 Antibodies) exit from the pluripotency state and initiate their differentiation processes.
During embryonic stem cell differentiation, an endogenous Wnt (show WNT2 Antibodies)-mediated burst in Snail1 expression regulates neuroectodermal fate while playing a role in epiblast stem cell exit and the consequent lineage fate decisions that define mesoderm commitment.
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.
snail homolog 1
, snail like protein
, Protein snail-like protein 1
, snail homolog 1 (Drosophila)
, snail 1 homolog
, 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
, protein sna
, protein snail homolog 1
, snail 1 zinc finger protein
, snail 1, zinc finger protein
, zinc finger protein SNAI1