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- rabbit polyclonal IgG, 200 µg/ml
- epitope mapping within a highly divergent domain of Gαt1(Gαrod transducin) of human origin
- recommended for detection of Gα t1 of mouse, rat, human and cow origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine, bovine and porcine
- blocking peptide, sc-389 P
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Gα t1 Background Information Heterotrimeric G proteins function to relay information from cell surface receptors to intracellular effectors (1). Each of a very broad range of receptors specifically detects an extracellular stimulus (a photon, pheromone, odorant, hormone or neurotransmitter) while the effectors (i.e., adenyl cyclase), which act to generate one or more intracellular messengers, are less numerous. In mammals, G protein å, ∫ and © polypeptides are encoded by at least 16, 4 and 7 genes, respectively (2-5). Most interest in G proteins has been focused on their å subunits, since these proteins bind and hydrolyze GTP and most obviously regulate the activity of the best studied effectors. Four distinct classes of Ga subunits have been identified; these include Gs, Gi, Gq and Gå 12/13 (3,4). The Gi class comprises all the known a subunits that are susceptible to pertussis toxin modifications, including Gå i-1, Gå i-2, Gå i-3, Gå o, Gå t1, Gå t2, Gå z and Gå gust (4). In the well characterized visual system, photorhodopsin catalyzes the exchange of guanine nucleotides bound to the visual transducin Gå subunits (Gå ti in rod cells and Gå t2 in cone cells) (6).
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See how others have used Gα t1 (K-20): sc-389 antibody and or Gα t1 (K-20) antibody conjugates.
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Gα t1 (K-20)
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Gα t1 (K-20): sc-389. Western blot analysis of Gα t1 expression in rat (A) and cow (B) brain extracts.
Gα t1 (K-20): sc-389. Western blot analysis of Gα t1 expression in rat brain tissue extract.
G α t1 (K-20): sc-389. Western blot analysis of G α t1 expression in non-transfected: sc-117752 (A) and mouse G α t1 transfected: sc-120374 (B) 293T whole cell lysates.
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