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The TAS1R3 gene encodes the human homolog of mouse Sac, a major determinant of differences between sweet-sensitive and -insensitive mouse strains in their responsiveness to sucrose, saccharine, and other sweeteners (Max et al., 2001. Zusätzlich bieten wir Ihnen Taste Receptor, Type 1, Member 3 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal TAS1R3 Primary Antibody für IHC (p), WB - ABIN271134
Raliou, Grauso, Hoffmann, Schlegel-Le-Poupon, Nespoulous, Débat, Belloir, Wiencis, Sigoillot, Bano, Trotier, Pernollet, Montmayeur, Faurion, Briand: Human genetic polymorphisms in T1R1 and T1R3 taste receptor subunits affect their function. in Chemical senses 2011
Medaka T1R1 (zeige TAS1R1 Antikörper) and T1R3 show the highest degrees of identity to mammalian T1R1 (zeige TAS1R1 Antikörper) and T1R3, respectively.
discovery of a gene regulatory network related to the porcine umami taste receptor TAS1R1 (zeige TAS1R1 Antikörper)/TAS1R3
The gene was shown to reside on swine chromosome 6q22-->q23, from which three types of mRNAs were generated. High expressions of TAS1R3 were revealed in tongue, kidney, and testis
We observe that binding of agonists to VFD2 of TAS1R2 (zeige TAS1R2 Antikörper) leads to major conformational changes to form a TM6/TM6 interface between TMDs of TAS1R2 (zeige TAS1R2 Antikörper) and TAS1R3, which is consistent with the activation process observed biophysically on the metabotropic glutamate receptor 2 (zeige GRM2 Antikörper) homodimer.
Regarding "consumption of carbohydrates (% energy) and higher amount of sweet foods, respectively...no associations were found for the TAS1R3 alleles."
The molecular anatomy of sweet taste receptor dimers T1R2 (zeige TAS1R2 Antikörper)-T1R3 has been presented.
TAS1R3 gene rs307355 polymorphism found independent risk factor for dental caries experience by logistic regression & increased risk of caries. Moderate caries (4-7 caries) found to be associated w/TAS1R3 rs307355 heterozygous genotype
T1R3 gene expression in the tongue is suppressed by chemotherapy.
The transcripts of TAS1R3 and UCN2 (zeige UTS2 Antikörper) in peripheral blood cells may be considered potential biomarkers of consumption of sugary and fatty food, respectively, to complement data of food-intake questionnaires.
human and mouse membrane trafficking systems for sweet taste receptors T1r2 (zeige TAS1R2 Antikörper) and T1r3
A complex molecular mechanism involving changes in the properties of both the orthosteric and non-orthosteric sites of T1R1 (zeige TAS1R1 Antikörper) underlies the determination of ligand specificity in mammalian T1R1 (zeige TAS1R1 Antikörper)/T1R3.
effects of artificial sweeteners on adipose tissue may be largely independent of the classical sweet taste receptors, T1R2 (zeige TAS1R2 Antikörper) and T1R3
Five amino acid residues in cysteine-rich domain of human T1R3 were involved in the response for sweet-tasting protein, thaumatin
T1R1 (zeige TAS1R1 Antikörper)/T1R3 modulates the mTOR (zeige FRAP1 Antikörper) pathway to regulate milk protein synthesis in the mouse mammary gland in vivo.
Data, including data from studies with mutant and knockout mice, suggest that Tas1R3 and Tas1R2 (zeige TAS1R2 Antikörper) are expressed endogenously in osteoclast stem cells; their expression levels parallel robust increase in osteoclast biomarker Ctsk (zeige CTSK Antikörper) during osteoclast differentiation. Tas1R3 is expressed in undifferentiated bone marrow stromal cells and its expression is maintained during osteogenic differentiation. (Ctsk (zeige CTSK Antikörper) = cathepsin K (zeige CTSK Antikörper))
results suggest that the T1R3 homomeric sweet taste receptor negatively regulates adipogenesis through Galphas (zeige GNAS Antikörper)-mediated microtubule disassembly and consequent activation of the Rho/ROCK pathway.
results implicate each subunit of the T1R2 (zeige TAS1R2 Antikörper)+T1R3 dimer in the behavioral response to P-containing taste compounds
T1r3 was upregulated in the adipose tissue of wild type mice in response to high fat/low carbohydrate diet, and their expression positively correlated with fat mass and glucose intolerance.
T1R3 and alpha-gustducin (zeige GNAT3 Antikörper) exhibited a stage-dependent expression pattern during mouse development, and a cell-specific pattern during the spermatogenic cycle.
Low concentration of endogenous GC is necessary and sufficient for induction of T1R3 expression. Higher concentrations may inhibit such induction. This inhibitory effect may be due, at least in part, to a direct action of GC on taste cells.
T1R1/T1R3 have roles in regulating ERK1/2 and mTORC1 in MIN6 cells
Mice possess two taste transduction pathways for sugars. One mediates behavioral attraction to sugars and requires an intact T1r2 (zeige TAS1R2 Antikörper)+T1r3. The other mediates cephalic phase insulin (zeige INS Antikörper) release but does not require an intact T1r2 (zeige TAS1R2 Antikörper)+T1r3.
Taken together, our study raises the possibility that MyoD (zeige MYOD1 Antikörper) and Myogenin (zeige MYOG Antikörper) might control skeletal muscle metabolism and homeostasis through the regulation of T1R3 promoter activity.
The TAS1R3 gene encodes the human homolog of mouse Sac, a major determinant of differences between sweet-sensitive and -insensitive mouse strains in their responsiveness to sucrose, saccharine, and other sweeteners (Max et al., 2001
taste receptor type 1 member 3
, taste receptor, type 1, member 3
, sweet taste receptor T1R3
, saccharin preference protein
, taste receptor T1R3