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p-ERK 1/2 (Thr 177 / Thr 160)-R Antibody: sc-23759-R |
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- rabbit polyclonal IgG, 200 µg/ml
- recommended for detection of Thr 177 and Thr 160 dually phosphorylated ERK 1 and ERK 2 of mouse, rat and human origin by WB, IP, IF and ELISA
- blocking peptide, sc-23759 P
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ERK 1/2 Background Information The activation of signal transduction pathways by growth factors, hormones and neurotransmitters is mediated through two closely related MAP kinases, p44 and p42, designated extracellular-signal related kinase 1 (ERK 1) and ERK 2, respectively. ERK proteins are regulated by dual phosphorylation at Tyrosine 204 and 187 and Threonine 177 and 160 residues mapping within a characteristic Thr-Glu-Tyr motif. Phosphorylation at both the Threonine 202 and Tyrosine 204 residues of ERK1 and Threonine 185 and Tyrosine 187 residues of ERK2 is required for full enzymatic activation. The structural consequences of dual-phosphorylation in the ERK2 include active site closure, alignment of key catalytic residues that interact with ATP, and remodeling of the activation loop. In response to activation, MAP kinases phosphorylate downstream components on serine and threonine. Upstream MAP kinase regulators include MAP kinase kinase (MEK), MEK kinase and Raf-1. The ERK family has three additional members: ERK 3, ERK 5 and ERK 6.
| p-ERK 1/2 (Thr 177 / Thr 160)-R Product Citations |
See how others have used p-ERK 1/2 (Thr 177 / Thr 160)-R: sc-23759-R antibody and or p-ERK 1/2 (Thr 177 / Thr 160)-R antibody conjugates.
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p-ERK 1/2 (Thr 177 / Thr 160)-R
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Western blot analysis of phosphorylated ERK 1/2 expression in untreated (A) and PDGF-treated (B,C) NIH/3T3 whole cell lysates. Blots were probed with p-ERK 1/2 (Thr 177 / Thr 160)-R: sc-23759-R (A,B) and p-ERK 1/2 (Thr 177 / Thr 160)-R: sc-23759-R preincubated with its cognate phosphorylated peptide (C).
p-ERK 1/2 (Thr 177/Thr 160)-R: sc-23759-R. Immunofluorescence staining of methanol-fixed NIH/3T3 cells showing nuclear localization.
p-ERK 1/2 (Thr 177/Thr 160)-R: sc-23759-R. Western blot analysis of ERK 1/2 phosphorylation in untreated (A), UV irradiated (B) and UV irradiated and lambda protein phosphatase treated (C) HeLa whole cell lysates.
Western blot analysis of ERK 1/2 phosphorylation in untreated (A, D), PMA treated (B, E) and PMA and lambda protein phosphatase treated (C, F) Jurkat whole cell lysates. Antibodies tested include p-ERK 1/2 (Thr 177/Thr 160)-R: sc-23759-R (A, B, C) and ERK 2 (K-23): sc-153 (D, E, F).
Western blot analysis of ERK 1/2 phosphorylation in untreated (A, C), and lambda protein phosphatase treated (B, D) HeLa whole cell lysates. Antibodies tested include p-ERK 1/2 (Thr 177/Thr 160)-R: sc-23759-R (A, B) and ERK 2 (K-23): sc-153 (C, D).
Western blot analysis of ERK 1/2 phosphorylation in untreated (A, D), UV irradiated (B, E) and UV irradiated and lambda protein phosphatase treated (C, F) HeLa whole cell lysates. Antibodies tested include p-ERK 1/2 (Thr 177/Thr 160)-R: sc-23759-R (A, B, C) and ERK 2 (K-23): sc-153 (D, E, F).
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