English
Phosphoserine Antibody: ATTO 390
Rabbit Anti-Phosphoserine Polyclonal
Artikelnummer
STRSPC-149F-A390
Verpackungseinheit
400 µl
Hersteller
Stressmarq Biosciences
Verfügbarkeit:
wird geladen...
Preis wird geladen...
Target: Phosphoserine
Conjugate: ATTO 390
Product Type: Polyclonal
Immunogen: Phosphoserine conjugated to KLH, and phosvitin mixture
Purification: Peptide Affinity Purified
Storage Buffer: PBS, 50% glycerol, 0.01% sodium azide *Storage buffer may change when conjugated
Concentration: 0.25 mg/ml
Specificity: Detects proteins phosphorylated on serine residues. Does not cross-react with phosphotyrosine.
Scientific Background: Protein phosphorylation is an important posttranslational modification that serves many key functions to regulate a protein's activity, localization, and protein-protein interactions. Phosphorylation is catalyzed by various specific protein kinases, which involves removing a phosphate group from ATP and covalently attaching it to to a recipient protein that acts as a substrate. Most kinases act on both serine and threonine; others act on tyrosine, and a number (dual specificity kinases) act on all three. Because phosphorylation can occur at multiple sites on any given protein, it can therefore change the function or localization of that protein at any time (1). Changing the function of these proteins has been linked to a number of diseases, including cancer, diabetes, heart disease, inflammation and neurological disorders (2-4).
References: 1. Goto H. et al. (2005) Nature Cell Biology 8: 180-187.2. Blume-Jensen P. and Hunter T. (2001) Nature 411: 355-365.3. Downward J. (2001) Nature 411: 759-762.4. Pawson T. and Saxton T.M. (1999) Cell 97: 675-678.5. Ostrovsky P.C. (1995) Genes Dev. 9(16): 2034-2041.
Field of Use: Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
Conjugate: ATTO 390
Product Type: Polyclonal
Immunogen: Phosphoserine conjugated to KLH, and phosvitin mixture
Purification: Peptide Affinity Purified
Storage Buffer: PBS, 50% glycerol, 0.01% sodium azide *Storage buffer may change when conjugated
Concentration: 0.25 mg/ml
Specificity: Detects proteins phosphorylated on serine residues. Does not cross-react with phosphotyrosine.
Scientific Background: Protein phosphorylation is an important posttranslational modification that serves many key functions to regulate a protein's activity, localization, and protein-protein interactions. Phosphorylation is catalyzed by various specific protein kinases, which involves removing a phosphate group from ATP and covalently attaching it to to a recipient protein that acts as a substrate. Most kinases act on both serine and threonine; others act on tyrosine, and a number (dual specificity kinases) act on all three. Because phosphorylation can occur at multiple sites on any given protein, it can therefore change the function or localization of that protein at any time (1). Changing the function of these proteins has been linked to a number of diseases, including cancer, diabetes, heart disease, inflammation and neurological disorders (2-4).
References: 1. Goto H. et al. (2005) Nature Cell Biology 8: 180-187.2. Blume-Jensen P. and Hunter T. (2001) Nature 411: 355-365.3. Downward J. (2001) Nature 411: 759-762.4. Pawson T. and Saxton T.M. (1999) Cell 97: 675-678.5. Ostrovsky P.C. (1995) Genes Dev. 9(16): 2034-2041.
Field of Use: Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
| Artikelnummer | STRSPC-149F-A390 |
|---|---|
| Hersteller | Stressmarq Biosciences |
| Hersteller Artikelnummer | SPC-149F-A390 |
| Green Labware | Nein |
| Verpackungseinheit | 400 µl |
| Mengeneinheit | STK |
| Reaktivität | Various species |
| Klonalität | Polyclonal |
| Methode | Immunofluorescence, Immunoprecipitation, Western Blotting, ELISA, Immunohistochemistry, Immunocytochemistry |
| Wirt | Rabbit |
| Produktinformation (PDF) | Download |
| MSDS (PDF) | Download |
Verwandte Artikel
Markieren Sie die Artikel, um Sie dem Warenkorb hinzuzufügen oder
Immer für Sie da
Gernot Ensinger, M.Sc.
Laurent Haze
