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Human GLUT1 ELISA Kit for Sandwich ELISA - ABIN416906
Prabhulkar, de la Zerda, Paranjape, Awdeh: Single step nanoplasmonic immunoassay for the measurement of protein biomarkers. in Biosensors 2015
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UCP2 stimulates hnRNPA2/B1, GLUT1 and PKM2 expression and sensitizes pancreatic cancer cells to glycolysis inhibition.
ablation of Glut1 attenuated apoptosis and increased drug resistance via upregulation of p-Akt (show AKT1 ELISA Kits)/p-GSK-3beta (show GSK3b ELISA Kits) (Ser9)/beta-catenin (show CTNNB1 ELISA Kits)/survivin (show BIRC5 ELISA Kits).
Data show that SALL4 (show SALL4 ELISA Kits) promotes the expression of Glut1 and open chromatin through a HP1alpha (show CBX5 ELISA Kits)-dependent mechanism.
Results show that PPARalpha (show PPARA ELISA Kits) directly targeted the consensus PPRE motif of Glut1 promoter region resulting in Glut1 transcription repression leding to decreased influx of glucose in cancer cells.
Strong GLUT1 staining was inversely associated with circulating levels of fasting glucose in high grade serous ovarian cancer.
Results show that resistin (show RETN ELISA Kits) down-regulates the transcription of GLUT1 by suppressing the expression of PPARG (show PPARG ELISA Kits), thus causing impaired glucose transportation in endothelial cell layers.
Metabolically active CD4 (show CD4 ELISA Kits)+ T cells expressing Glut1 and OX40 (show TNFRSF4 ELISA Kits) preferentially harbor HIV during in vitro infection.
we found that PPARdelta (show PPARD ELISA Kits) directly regulated neutral amino acid transporter (show SLC6A19 ELISA Kits) SLC1 (show MCHR1 ELISA Kits)-A5 (solute carrier family 1 member 5 (show SLC1A5 ELISA Kits)) and glucose transporter-1 (Glut1) gene transcription, leading to uptake of glucose and amino acid, activation of mTOR (show FRAP1 ELISA Kits) signaling, and tumor progression. In contrast, silence of PPARdelta (show PPARD ELISA Kits) or its antagonist inhibited this event.
SLC2A1/GLUT1 is expressed late in the adenoma-carcinoma sequence during carcinogenesis in intraductal papillary mucinous neoplasms of the pancreas.
Paraoxonase 2 (show PON2 ELISA Kits) facilitates pancreatic ductal cancer growth and metastasis by stimulating GLUT1-mediated glucose transport.
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 (show ARAP2 ELISA Kits) 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 shuttling to autophagosomes during metabolic stress facilitates retromer-dependent GLUT1 trafficking.
inhibition of GLUT1 activity and/or expression is shown to impair TGF-beta (show TGFB1 ELISA Kits)-driven fibrogenic processes, including cell proliferation and production of profibrotic mediators
B cell leukemia-induced inhibition of T cell Akt (show AKT1 ELISA Kits)/mTORC1 signaling and glucose metabolism drives T cell dysfunction; metabolic defects included reduced Akt (show AKT1 ELISA Kits)/mammalian target of rapamycin (show FRAP1 ELISA Kits) complex 1 (mTORC1) signaling, decreased expression of the glucose transporter Glut1 and hexokinase 2 (show HK2 ELISA Kits), 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 (show HIF1A ELISA Kits), alpha subunit (show POLG ELISA Kits)) mediating hyperglycemia-induced extracellular matrix accumulation in kidney via regulation of Nox4 (show NOX4 ELISA Kits) (NADPH oxidase (show NOX1 ELISA Kits) type 4) expression in nephropathy due to diabetes type 1.
CRISPR/Cas9-mediated disruption of the Hdac2 gene increased Slc2a1 expression, suggesting that it is one of the responsible histone deacetylases (HDACs). These results confirm that b-OHB is a HDAC inhibitor and show that b-OHB plays an important role in fasting-induced epigenetic activation of a glucose transporter gene in the brain.
Taken together, the data suggest that curcumin binds directly to GLUT1 at a site that overlaps with the cytochalasin B binding site and thereby inhibits glucose transport.
Glut-1 expression globally depended on histological subtypes and the staining patterns (diffuse or zonal) were different between thymic carcinomas and type B3 thymomas
Glut-1 glucose transporter expression in esophageal squamous cell carcinoma is associated with tumor aggressiveness.
Glucose transporter 1 transcript levels were higher in the right ventricle than the left ventricle.
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 (show SLC2A3 ELISA Kits) expression in nonclassical monocytes was unaltered during differentiation into macrophages. GLUT4 (show SLC2A4 ELISA Kits) mRNA was only detectable in unstimulated macrophages. Neither monocytes nor macrophages were insulin (show INS ELISA Kits) 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 (show HSP90 ELISA Kits).eNOS (show NOS3 ELISA Kits) preserves mitochondrial respiration in hyperglycemic endothelial cells by down-regulating Glut-1 and up-regulating G6PD (show G6PD ELISA Kits) 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
, glucose transporter
, glucose transporter 1
, lethal (3) S007412
, solute carrier family 2 (facilitated glucose transporter), member 1
, solute carrier family 2 member 1
, excitatory amino acid transporter 1
, glial glutamate transporter
, glutamate transporter
, glutamate/aspartate transporter
, sodium-dependent glutamate/aspartate transporter 1
, solute carrier family 1, member 3
, glucose transporter protein
, glucose transporter type 1
, solute carrier family 2 (facilitated glucose transporter), member 1 L homeolog
, glucose transport protein