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anti-Human E-cadherin Antibodies:
anti-Rat (Rattus) E-cadherin Antibodies:
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Human Polyclonal E-cadherin Primary Antibody for CyTOF, FACS - ABIN4899267
Ihermann-Hella, Lume, Miinalainen, Pirttiniemi, Gui, Peränen, Charron, Saarma, Costantini, Kuure: Mitogen-activated protein kinase (MAPK) pathway regulates branching by remodeling epithelial cell adhesion. in PLoS genetics 2014
Show all 14 Pubmed References
Human Polyclonal E-cadherin Primary Antibody for WB - ABIN3042914
Duan, Lin, Li, Ding, Qian, Zhang, Ge, Fan, Li: Effects of inhibition of hedgehog signaling on cell growth and migration of uveal melanoma cells. in Cancer biology & therapy 2014
Show all 12 Pubmed References
Human Polyclonal E-cadherin Primary Antibody for IHC (fro), IHC (p) - ABIN3043808
Li, Lv, Wu, Zhang, Liu, Liu: Dexamethasone prevents monocyte-induced tubular epithelial-mesenchymal transition in HK-2 cells. in Journal of cellular biochemistry 2013
Show all 12 Pubmed References
Human Monoclonal E-cadherin Primary Antibody for ICC, IHC (fro) - ABIN335399
Frixen, Behrens, Sachs, Eberle, Voss, Warda, Löchner, Birchmeier: E-cadherin-mediated cell-cell adhesion prevents invasiveness of human carcinoma cells. in The Journal of cell biology 1991
Show all 8 Pubmed References
Human Monoclonal E-cadherin Primary Antibody for FACS, ICC - ABIN807921
Armeanu, Bühring, Reuss-Borst, Müller, Klein: E-cadherin is functionally involved in the maturation of the erythroid lineage. in The Journal of cell biology 1995
Show all 12 Pubmed References
Human Monoclonal E-cadherin Primary Antibody for FACS, ICC - ABIN457413
Pece, Gutkind: Signaling from E-cadherins to the MAPK pathway by the recruitment and activation of epidermal growth factor receptors upon cell-cell contact formation. in The Journal of biological chemistry 2001
Show all 10 Pubmed References
Human Monoclonal E-cadherin Primary Antibody for FACS, ICC - ABIN457304
Pece, Chiariello, Murga, Gutkind et al.: Activation of the protein kinase Akt/PKB by the formation of E-cadherin-mediated cell-cell junctions. Evidence for the association of phosphatidylinositol 3-kinase with the E-cadherin adhesion ... in The Journal of biological chemistry 1999
Show all 10 Pubmed References
Human Monoclonal E-cadherin Primary Antibody for FACS, ICC - ABIN457335
Takeichi: Cadherin cell adhesion receptors as a morphogenetic regulator. in Science (New York, N.Y.) 1991
Show all 10 Pubmed References
Human Polyclonal E-cadherin Primary Antibody for CyTOF, FACS - ABIN4899263
Gaballah, Costea, Hills, Gollin, Harrison, Partridge: Tissue engineering of oral dysplasia. in The Journal of pathology 2008
Show all 7 Pubmed References
Human Monoclonal E-cadherin Primary Antibody for ELISA, FACS - ABIN4306576
Saulnier, Piscaglia, Puglisi, Barba, Arena, Pani, Alfieri, Gasbarrini: Molecular mechanisms underlying human adipose tissue-derived stromal cells differentiation into a hepatocyte-like phenotype. in Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2010
Show all 6 Pubmed References
Amla extract (Emblica officinalis, AE) decreases the gene and protein expression of IGF1R (show IGF1R Antibodies), a target of miR (show MLXIP Antibodies)-375, and SNAIL1 (show SNAI1 Antibodies), a transcription factor that represses E-cadherin expression.
Results show that CDH1 expression is significantly downregulated in human hepatocellular carcinoma (HCC (show FAM126A Antibodies)) tissues and inversely correlates with RARgamma expression. Also, the study shows that CDH1 expression is under the regulation of RARgamma.
patients with both abnormal expression of p0071 (show PKP4 Antibodies) and E-cadherin (cytoplasmic expression) had a statistically significant shorter survival than the patients without both abnormal expression (P < 0.05).
The levels of CDC20 (show CDC20 Antibodies) and CylinB1 increased and the levels of Ku70 (show XRCC6 Antibodies) and APC3 decreased after irradiation. APC (show APC Antibodies)/C(Cdh1) is involved in regulation of radiosensitivity in human NPC (show NPC1 Antibodies) CNE-1 cells.
human pluripotent stem cells are subject to matrix metalloproteinase-dependent E-cadherin ectodomain shedding.
Study shows that the protein level of E-CAD is indirectly regulated by MIR (show MLXIP Antibodies)-193a in non-small cell lung cancers through downregulation of WT1 (show WT1 Antibodies).
EZH2 (show EZH2 Antibodies) is recruited to the E-cadherin promoter by the long non-coding RNA, MALAT-1 (metastasis associated in lung adenocarcinoma transcript 1), where it represses E-cadherin expression
Data indicate that E-cadherin and caspase-3 (show CASP3 Antibodies) were targets of miR (show MLXIP Antibodies)-421, which was up-regulated by HIF-1alpha (show HIF1A Antibodies).
Neutrophil elastase has the capacity to cleave E-cad and interfere with its cell-cell adhesion function in acutely injured lung epithelium.
ANP (show NPPA Antibodies) inhibits TGF-beta1 (show TGFB1 Antibodies)-induced EMT (show ITK Antibodies) in 16HBE-14o and A549 cells through cGMP/PKG (show PRKG1 Antibodies) signaling, by which it targets TGF-beta1 (show TGFB1 Antibodies)/Smad3 (show SMAD3 Antibodies) via attenuating phosphorylation of Smad3 (show SMAD3 Antibodies). These findings suggest the potential of ANP (show NPPA Antibodies) in the treatment on pulmonary diseases with airway remodeling.
These collective findings indicate that loss of Bit1 (show PTRH2 Antibodies) expression contributes to the acquisition of malignant phenotype of human lung epithelial cells via Erk (show MAPK1 Antibodies) activation-induced suppression of E-cadherin expression.
In zebrafish, E-cadherin is expressed in lens epithelium, whereas N-cadherin (show CDH2 Antibodies) is required for lens fiber growth
These data indicate that emi1 (show FBXO5 Antibodies) deficiency-induced defects in vivo are due to the dysregulation of an APC/C-Cdh1 molecular axis.
without Chp (show CHP Antibodies) signaling, E-cadh shifts to intracellular vesicles rather than the adhesive contacts needed for directed cell movement during epiboly
Downregulation of E-cadherin gene may cause omphalocele in the Cd chick model by disrupting CRT (show CALR Antibodies)-mediated Ca(2 (show CA2 Antibodies)+) signaling and AJs.
analyzed expression patterns of three zebrafish classical (type I) cadherins (cadherin-1, -2, and -4) in the embryonic zebrafish cranial ganglia and lateral line system
cadherin-1 is detected in the epidermis of the embryonic limb buds and the larval pectoral fins of zebrafish
hab/E-cadherin is necessary for the cell rearrangements that spread the teleost blastoderm over the yolk
Lgl2 (show LLGL2 Antibodies) and E-cadherin act antagonistically to control the localisation of integrin alpha 6 (show ITGA6 Antibodies) during the formation of hemidesmosomes in the developing epidermis
Galpha12/13 regulate epiboly by inhibiting E-cadherin activity and modulating the actin cytoskeleton.
E-cadherin mRNA/protein were up-regulated in all flutamide-treated corpus luteum of mid- and late pregnancy.
In pig kidney, strong E-cadherin expression was observed in the basolateral plasma membrane of the tubular epithelial cells. E-cadherin immunolabeling was not detected in glomeruli or blood vessels of pig kidney.
Localisation of NANOG (show NANOG Antibodies), OCT4 (show POU5F1 Antibodies), and E-CADHERIN in porcine pre- and peri (show PLIN1 Antibodies)-implantation embryos.
The epiblast expressed epithelial markers, MUC1 (show MUC1 Antibodies) and E-CADHERIN, and the pluripotency markers, DNMT3B (show DNMT3B Antibodies) and CRIPTO (show TDGF1 Antibodies).
E-cadherin has a role in cranial neural crest migration in Xenopus laevis
the switch from E- to N-cadherin (show CDH2 Antibodies) during epithelial-mesenchymal transition is essential for acquisition of Contact inhibition of locomotion behavior.
Moderate attenuation of C-cadherin function affects cell adhesion but not gastrulation.
Because paraxial protocadherin and C-cadherin do not directly interact nor form a joint complex with Fz7, Wnt-11 triggers formation of two distinct complexes that act in parallel to reduce cell adhesion by hampering clustering of C-cadherin.
The functional and physical relationships between PAPC, FLRT3, and C-cadherin, was investigated.
PAPC mediates these functions by down-regulating the adhesion activity of C-cadherin.
Results suggest that the basis for cell segregation during morphogenesis does not map exclusively to protein-level differences in E-, N-, or C-cadherin adhesion.
G-protein-coupled receptors control cortical actin assembly by controlling the amount of cadherin expressed on the cell surface.
Two stage cadherin kinetics require multiple extracellular domains but not the cytoplasmic region
Data show that the intracellular domain of PAPC (Protocadherin) interacts with Sprouty (Spry), and upon binding to PAPC, Spry function is inhibited and PCP signaling is enhanced.
Study shows that over time, epithelial tumor cells undergo epithelial state to a mesenchymal-like state changes (including loss of E-cadherin expression) during primary tumor growth and E-cadherin is re-expressed in metastatic tumor cells.
This study reveals a novel role for Cdh1 in craniofacial development through promoting APC (show APC Antibodies)-dependent non-proteolytic ubiquitination and activation of Gsc (show GSC Antibodies).
We describe a mouse model in which inducible deletion of E-cadherin in prostate luminal cells results in their apoptotic cell death by anoikis, in the absence of phenotypic effects in the surrounding stroma
Our results provide a mechanistic explanation for the spontaneous emergence of pluripotent cells from GSC (show GSC Antibodies) cultures; namely, rare GSCs upregulate CDH1 and initiate MET, processes normally kept in check by ZEB1 (show ZEB1 Antibodies) and TGF-beta (show TGFB1 Antibodies) signaling, thereby ensuring germ cells are protected from aberrant acquisition of pluripotency.
PTEN (show PTEN Antibodies) loss in E-cadherin-deficient mouse mammary epithelial cells rescues apoptosis and results in development of classical invasive lobular carcinoma.
Low CDH1 expression is associated with Gastric Tumorigenesis.
These observations highlight the relevance of APC (show APC Antibodies)/C cofactor Cdh1 activity during G1 to ensure an adequate supply of deoxynucleoside triphosphates to the replisome, prevent replication stress and the resulting chromosomal breaks and, ultimately, suppress tumorigenesis.
Ilk (show ILK Antibodies) and ELMO2 (show ELMO2 Antibodies) modulate recycling endosomes in keratinocytes undergoing intercellular adhesion mediated through cell-cell contacts, including E-cadherin-based adherens junctions.
JNK (show MAPK8 Antibodies) signaling, which is inversely correlated with WNT4 (show WNT4 Antibodies), plays an important role in perinatal germline cyst breakdown and primordial follicle formation by regulating E-cadherin junctions between oocytes in mouse ovaries.
Transfection of zygotes with 100 and 200 nM E-cadherin siRNA led to a 72 and 38% reduction, respectively, in E-cadherin mRNA relative abundance in Day 7 blastocysts compared with controls.
E-cadherin and beta-catenin (show CTNNB1 Antibodies) were distributed not only at the cell to cell boundary but throughout the cytoplasm in binucleate trophoblast cells
Results describe the effect of suppression of connexin 43 (show GJA1 Antibodies) and E-cadherin on the development, mRNA and protein expression of bovine blastocysts cultured in vitro or in vivo.
This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium dependent cell-cell adhesion glycoprotein comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Mutations in this gene are correlated with gastric, breast, colorectal, thyroid and ovarian cancer. Loss of function is thought to contribute to progression in cancer by increasing proliferation, invasion, and/or metastasis. The ectodomain of this protein mediates bacterial adhesion to mammalian cells and the cytoplasmic domain is required for internalization. Identified transcript variants arise from mutation at consensus splice sites.
, cadherin 1, E-cadherin (epithelial)
, calcium-dependent adhesion protein, epithelial
, cell-CAM 120/80
, epithelial cadherin
, hypothetical protein LOC368517
, cadherin 1, epithelial
, half baked
, hypothetical protein LOC368516
, cadherin 1, type 1, E-cadherin (epithelial)
, C-cadherin (EP-cadherin)
, liver cell adhesion molecule
, liver cell adhesion protein
, Epithelial cadherin