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Gα i-1/2/3 (N-20) Antibody: sc-26761 |
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- goat polyclonal IgG, 200 µg/ml
- epitope mapping near the N-terminus of Gα i-1 of human origin
- recommended for detection of Guanine nucleotide binding proteins Gα i-1,Gα i-2 and Gα i-3 of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine, bovine, porcine and avian
- blocking peptide, sc-26761 P
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Gα i-1/2/3 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-1/2/3 (N-20) Product Citations |
See how others have used Gα i-1/2/3 (N-20): sc-26761 antibody and or Gα i-1/2/3 (N-20) antibody conjugates.
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Gα i-1/2/3 (N-20)
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Gα i-1/2/3 (N-20): sc-26761. Western blot analysis of Gα i expression in rat brain (A) and mouse brain (B) tissue extracts.
Gα i-1/2/3 (N-20): sc-26761. Immunofluorescence staining of methanol-fixed KNRK cells showing membrane localization.
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