| Reactivity | HuSpecies Glossary |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Host | Sheep |
| Conjugate | Alexa Fluor 405 |
| Immunogen | E. coli-derived recombinant human RGS8 Asn10-Thr76 Accession # P57771 |
| Specificity | Detects human RGS8 in direct ELISAs and Western blots. In direct ELISAs, less than 1% cross-reactivity with recombinant human RGS4 is observed. |
| Isotype | IgG |
| Clonality | Polyclonal |
| Host | Sheep |
| Purity Statement | Antigen Affinity-purified |
| Innovator's Reward | Test in a species/application not listed above to receive a full credit towards a future purchase. |
| Storage | Protect from light. Do not freeze. 12 months from date of receipt, 2 to 8 °C as supplied |
| Buffer | Supplied 0.2mg/ml in 1X PBS with RDF1 and 0.09% Sodium Azide |
RGS8 (Regulator of G-protein signaling 8) is a 22-23 kDa (predicted) member of the B/R4 subfamily, RGS family of proteins. It is expressed in NK cells and neurons, particularly cerebellar Purkinje cells, and is known to regulate GPCR signaling. When GPCRs are activated, a GPCR cytoplasmic domain associated G alpha beta gamma heterotrimer dissociates in response to GTP binding. This generates G alpha :GTP and G beta gamma dimers that initiate downstream signaling. G alpha has GTPase activity, and when GTP is hydrolyzed, the G alpha beta gamma trimer reforms and stops signaling. RGS8 potentiates G alpha GTP hydrolase activity, particularly when associated with M1 muscarinic acetylcholine receptors. Human RGS8 is 180 amino acids (aa) in length, and is characterized by the presence of one RGS domain (aa 56-171), and an N-terminal GPCR binding motif (aa 6-9). There is one splice variant that shows a 27 aa substitution for aa 1-9. Expression of this variant may negatively impact its regulation of G alpha -coupled responses. Over aa 10-76, human RGS8 shares 98% aa identity with mouse RGS8.
Secondary Antibodies |
Isotype Controls |
|
RNA-binding protein Staufen1 conspires with Atxn2 in stress granules to cause neurodegeneration by dysregulating RNA metabolism By Jamshed Arslan Pharm.D. Spinocerebellar ataxia type 2 (SCA2) is a movement disorder characterized by neurodegeneration. The cause of this autosomal dominant disease is a mutation in the RNA processing gene Atxn2,... Read full blog post. |
The concentration calculator allows you to quickly calculate the volume, mass or concentration of your vial. Simply enter your mass, volume, or concentration values for your reagent and the calculator will determine the rest.