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Human Polyclonal GLUT1 Primary Antibody pour ELISA, ICC - ABIN152817
Minamishima, Moslehi, Bardeesy, Cullen, Bronson, Kaelin: Somatic inactivation of the PHD2 prolyl hydroxylase causes polycythemia and congestive heart failure. dans Blood 2008
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Human Polyclonal GLUT1 Primary Antibody pour ChIP, FACS - ABIN258123
Hergovich, Lisztwan, Thoma, Wirbelauer, Barry, Krek: Priming-dependent phosphorylation and regulation of the tumor suppressor pVHL by glycogen synthase kinase 3. dans Molecular and cellular biology 2006
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Human Monoclonal GLUT1 Primary Antibody pour CyTOF, FACS - ABIN4899145
Jain, Manuel, Khan, Ahuja, Quann, Wigdahl: DC-SIGN mediates cell-free infection and transmission of human T-cell lymphotropic virus type 1 by dendritic cells. dans Journal of virology 2009
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Human Polyclonal GLUT1 Primary Antibody pour IHC (p), WB - ABIN4886725
Xu, Bao, Zhou, Fan: Effect on the expression of MMP-2, MT-MMP in laryngeal carcinoma Hep-2 cell line by antisense glucose transporter-1. dans Archives of medical research 2012
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Human Monoclonal GLUT1 Primary Antibody pour FACS - ABIN4895661
Patsoukis, Bardhan, Chatterjee, Sari, Liu, Bell, Karoly, Freeman, Petkova, Seth, Li, Boussiotis: PD-1 alters T-cell metabolic reprogramming by inhibiting glycolysis and promoting lipolysis and fatty acid oxidation. dans Nature communications 2015
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Human Monoclonal GLUT1 Primary Antibody pour FACS - ABIN4895663
Prost, Relouzat, Spentchian, Ouzegdouh, Saliba, Massonnet, Beressi, Verhoeyen, Raggueneau, Maneglier, Castaigne, Chomienne, Chrétien, Rousselot, Leboulch: Erosion of the chronic myeloid leukaemia stem cell pool by PPARγ agonists. dans Nature 2015
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Human Polyclonal GLUT1 Primary Antibody pour FACS, ICC - ABIN5076961
Rodríguez-Espinosa, Rojas-Espinosa, Moreno-Altamirano, López-Villegas, Sánchez-García: Metabolic requirements for neutrophil extracellular traps formation. dans Immunology 2015
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Human Monoclonal GLUT1 Primary Antibody pour FACS - ABIN4895662
Feldhoff, Rueda, Moreno-Fernandez, Sauer, Jackson, Chougnet, Rupp: IL-1β induced HIF-1α inhibits the differentiation of human FOXP3+T cells. dans Scientific reports 2017
Human Monoclonal GLUT1 Primary Antibody pour FACS - ABIN4895659
Palmer, Ostrowski, Gouillou, Tsai, Yu, Zhou, Henstridge, Maisa, Hearps, Lewin, Landay, Jaworowski, McCune, Crowe: Increased glucose metabolic activity is associated with CD4+ T-cell activation and depletion during chronic HIV infection. dans AIDS 2014
Human Polyclonal GLUT1 Primary Antibody pour IHC, ELISA - ABIN1582249
Wang, Li, Gao, Lu, Zhang, Ma, Ye, Zhang: Cardiotrophin-1 (CTF1) ameliorates glucose-uptake defects and improves memory and learning deficits in a transgenic mouse model of Alzheimer's disease. dans Pharmacology, biochemistry, and behavior 2013
YAP1 (Montrer YAP1 Anticorps) interacted with TEAD1 (Montrer TEAD1 Anticorps), exerted their transcriptional control of the functional target, glucose transporter 1 (Glut1).
experiments mainly reveal that the CREB1 (Montrer CREB1 Anticorps) could affect glucose transport in glioma cells by regulating the expression of GLUT1, which controlled the metabolism of glioma and affected the progression of glioma.
These data provide new insights into the physiological relevance of GLUT1 multimerization as well as a new variant of bioluminescent Forster resonance energy transfer assay that is useful for measuring the interactions among other cell membrane proteins in live cells
Study demonstrated that the high mRNA level of both MCT1 (Montrer CMA1 Anticorps) and GLUT1 correlated with poor prognosis, high- Fuhrman grade clear-cell renal cell carcinoma (Montrer MOK Anticorps) and metabolic reprogramming.
GLUT1 and MCT1 (Montrer CMA1 Anticorps) membrane overexpression was significantly higher in Papillary Renal Cell carcinoma (Montrer MOK Anticorps)
HOTAIR promoted glycolysis by upregulating glucose transporter isoform 1 (GLUT1) and activating mammalian target of rapamycin (mTOR (Montrer FRAP1 Anticorps)) signaling.
In preeclampsia, placental GLUT1 expression and function are down-regulated at the apical plasma membrane of the syncytiotrophoblast.
High glut1 expression is associated with Pancreatic Cancer.
Study confirms the high expression of Glut-1 not only in endometrioid carcinomas but also in other carcinomas of endometrium including clear cell and serous types. Glut-1 expression can be used as a surrogate marker in differential diagnosis between hyperplasia with and without atypia.
This systematic review and meta-analysis indicated that the GLUT1 may serve as an ideal prognostic biomarker in various cancers.
Immunoreactivity of vGluT1 in continuous theta-burst stimulation (iTBS; cTBS (Montrer CTBS Anticorps)) repeated session (RS) decreased, while GLT-1 (Montrer SLC1A2 Anticorps) increased in cTBS (Montrer CTBS Anticorps) SS and cTBS (Montrer CTBS Anticorps) RS, compared to control
Expression of GLUT1 is stimulated by hyperglycemia and low oxygen supply, and this overexpression was associated with increased activity of GLUT1 in the cell membrane that contributes to the impairment of the RPE (Montrer RPE Anticorps) secretory function of PEDF (Montrer SERPINF1 Anticorps).
GLUT1 may play an important role in Prostate Cancer progression via mediating glycolysis and proliferation. There is potential crosstalk between GLUT1-mediated glycolysis and androgen sensitivity in Prostate Cancer.
ARAP2 (Montrer ARAP2 Anticorps) knockdown did not affect fatty acid uptake but reduced basal glucose uptake, total levels of the glucose transporter GLUT1, and GLUT1 levels in the plasma membrane and the lipid micro-domain fraction.
TBC1D5 (Montrer TBC1D5 Anticorps) shuttling to autophagosomes during metabolic stress facilitates retromer-dependent GLUT1 trafficking.
inhibition of GLUT1 activity and/or expression is shown to impair TGF-beta (Montrer TGFB1 Anticorps)-driven fibrogenic processes, including cell proliferation and production of profibrotic mediators
B cell leukemia-induced inhibition of T cell Akt (Montrer AKT1 Anticorps)/mTORC1 signaling and glucose metabolism drives T cell dysfunction; metabolic defects included reduced Akt (Montrer AKT1 Anticorps)/mammalian target of rapamycin (Montrer FRAP1 Anticorps) complex 1 (mTORC1) signaling, decreased expression of the glucose transporter Glut1 and hexokinase 2 (Montrer HK2 Anticorps), and reduced glucose uptake
This study demonstrates a strict requirement for GLUT1 in the early stages of mammary tumorigenesis in vitro and in vivo.
GLUT1-dependent glycolysis regulates fibrogenesis in aged lung.
Data (including data from studies using transgenic mice) suggest that Glut1 (glucose transporter type 1) is a critical downstream target of Hif1a (hypoxia-inducible factor 1 (Montrer HIF1A Anticorps), alpha subunit (Montrer POLG Anticorps)) mediating hyperglycemia-induced extracellular matrix accumulation in kidney via regulation of Nox4 (Montrer NOX4 Anticorps) (NADPH oxidase (Montrer NOX1 Anticorps) type 4) expression in nephropathy due to diabetes type 1.
pGlcT, together with MEX1, contributes significantly to the export of starch degradation products from chloroplasts in A. thaliana leaves and and that this starch-mediated pathway for photoassimilate export via pGlcT and MEX1 is essential for the growth and development of A. thaliana. [pGlcT]
Low GLUT1 and GLUT3 (Montrer SLC2A3 Anticorps) expression in nonclassical monocytes was unaltered during differentiation into macrophages. GLUT4 (Montrer SLC2A4 Anticorps) mRNA was only detectable in unstimulated macrophages. Neither monocytes nor macrophages were insulin (Montrer INS Anticorps) responsive.
the different conformations of the GLUT-1 transporter in luminal (blood facing) and abluminal (brain facing) membranes of bovine cerebral endothelial cells arise from differential phosphorylation of GLUT-1
Significant increases in GLUT1 gene expression were observed during early lactation.
Hyperthermia-induced Hsp90 (Montrer HSP90 Anticorps).eNOS (Montrer NOS3 Anticorps) preserves mitochondrial respiration in hyperglycemic endothelial cells by down-regulating Glut-1 and up-regulating G6PD (Montrer G6PD Anticorps) activity.
distinct domains of the glucose transporter GLUT1 mediate HTLV envelope binding and virus entry
Expression of GLUT1 was evaluated in LLC-PK1 cells grown on porous membranes for the development of an artificial kidney.
results suggest that glucose is transported to the axonal cleft intracytoplasmically and delivered to the cleft by GLUT1 transporters
This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia.
, glucose transporter type 1, erythrocyte/brain
, hepG2 glucose transporter
, human T-cell leukemia virus (I and II) receptor
, solute carrier family 2, facilitated glucose transporter member 1
, solute carrier family 2, member 1
, Solute carrier family 2 a 1 (facilitated glucose transporter) brain
, Solute carrier family 2, facilitated glucose transporter member 1
, solute carrier family 2 (facilitated glucose transporter), member 1
, solute carrier family 2 member 1
, glucose transporter protein
, glucose transporter type 1
, solute carrier family 2 (facilitated glucose transporter), member 1 L homeolog
, glucose transport protein