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- rabbit polyclonal IgG, 200 µg/ml
- epitope mapping with in a highly divergent domain of Gα i-1 of rat origin
- recommended for detection of Gα i-1 and, to a lesser extent, Gα i-2 and Gα i-3 of mouse, rat, human and cow origin by WB, IF and ELISA; also reactive with additional species, including equine, canine, bovine, porcine and avian
- blocking peptide, sc-391 P
- agarose conjugate for IP studies, sc-391 AC, 500 µg/0.25 ml agarose
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Gα i-1 Background Information Heterotrimeric G proteins function to relay information from cell surface receptors to intracellular effectors. Each of a very broad range of receptors specifically detects an extracellular stimulus (a photon, pheromone, odorant, hormone or neurotransmitter), whereas the effectors (i.e. adenyl cyclase), which act to generate one or more intracellular messengers, are less numerous. In mammals, G protein a, b and g subunits are encoded by at least sixteen, four and seven different genes, respectively. The a subunits bind to and hydrolyze GTP. G protein complexes expressed in different tissues contain distinct a, b and g subunits. Preferential associations between members of subunit families increase G protein functional diversity. 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 Gå subunits have been identified; these include Gs, Gi, Gq and Ga 12/13. 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. Of these, the three Ga i subtypes function to open atrial potassium channels.
| Gα i-1 (I-20) Product Citations |
See how others have used Gα i-1 (I-20): sc-391 antibody and or Gα i-1 (I-20) antibody conjugates.
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Gα i-1 (I-20)
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G α i-1 (I-20): sc-391. Western blot analysis of G α i-1 expression in bovine brain extract (A) and analysis of rat recombinant G α i-1: sc-4232 WB (B).
Gα i-1 (I-20): sc-391. Western blot analysis of Gα i-1 expression in SK-N-SH whole cell lysate.
Gα i-1 (I-20): sc-391. Western blot analysis of Gα i-1 expression in mouse brain tissue extract.
Gα i-1 (I-20): sc-391. Immunofluorescence staining of methanol-fixed HeLa cells showing cytoplasmic and nuclear localization.
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