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recombinant akt1 protein  (MedChemExpress)


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    MedChemExpress recombinant akt1 protein
    Recombinant Akt1 Protein, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/recombinant akt1 protein/product/MedChemExpress
    Average 93 stars, based on 9 article reviews
    recombinant akt1 protein - by Bioz Stars, 2026-03
    93/100 stars

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    Image Search Results


    ( A ) In silico screening of database(s) predicting kinase recognition motif in Su(H) S269 ; see . ( B ) In vitro assay screening 245 human Ser/Thr kinases for their ability to phosphorylate the beta-trefoil domain (BTD) domain of Su(H); see . ( C ) In vivo screen of 44 different Drosophila kinase mutants for crystal cell occurrence in third instar larvae; see , , and . ( D ) NanoLC/ESI mass spectrometry with active human kinases monitoring their ability to phosphorylate the given Su(H) peptide. PKCα phosphorylates S269, whereas AKT1, CAMK2D, and S6 kinase prefer T271. Spectra are shown in .

    Journal: eLife

    Article Title: Inhibition of the Notch signal transducer CSL by Pkc53E-mediated phosphorylation to fend off parasitic immune challenge in Drosophila

    doi: 10.7554/eLife.89582

    Figure Lengend Snippet: ( A ) In silico screening of database(s) predicting kinase recognition motif in Su(H) S269 ; see . ( B ) In vitro assay screening 245 human Ser/Thr kinases for their ability to phosphorylate the beta-trefoil domain (BTD) domain of Su(H); see . ( C ) In vivo screen of 44 different Drosophila kinase mutants for crystal cell occurrence in third instar larvae; see , , and . ( D ) NanoLC/ESI mass spectrometry with active human kinases monitoring their ability to phosphorylate the given Su(H) peptide. PKCα phosphorylates S269, whereas AKT1, CAMK2D, and S6 kinase prefer T271. Spectra are shown in .

    Article Snippet: Peptide, recombinant protein , Activated Akt1 , ProQinase , Cat# 1379-0000-2 , .

    Techniques: In Silico, In Vitro, In Vivo, Mass Spectrometry

    ( A ) MS/MS spectrum on the Su(H) phosphopeptide 262-ALFNRLRpSQTVSTRY-276 after treatment with activated human kinases PKC⍺. ( B–D ) MS/MS spectra of the Su(H) phosphopeptide 262-ALFNRLRSQpTVSTRY-276 after incubation with activated human AKT1 ( B ), CAMK2D ( C ), and S6 kinase ( D ), respectively. The phosphorylation at S8, corresponding to S269 and at T10, corresponding to T271 in Su(H) was confirmed by b- and y-ion series as indicated in blue and red, respectively. Neutral loss reactions of H 2 O and H 3 PO 4 from the precursor peptide are indicated in green.

    Journal: eLife

    Article Title: Inhibition of the Notch signal transducer CSL by Pkc53E-mediated phosphorylation to fend off parasitic immune challenge in Drosophila

    doi: 10.7554/eLife.89582

    Figure Lengend Snippet: ( A ) MS/MS spectrum on the Su(H) phosphopeptide 262-ALFNRLRpSQTVSTRY-276 after treatment with activated human kinases PKC⍺. ( B–D ) MS/MS spectra of the Su(H) phosphopeptide 262-ALFNRLRSQpTVSTRY-276 after incubation with activated human AKT1 ( B ), CAMK2D ( C ), and S6 kinase ( D ), respectively. The phosphorylation at S8, corresponding to S269 and at T10, corresponding to T271 in Su(H) was confirmed by b- and y-ion series as indicated in blue and red, respectively. Neutral loss reactions of H 2 O and H 3 PO 4 from the precursor peptide are indicated in green.

    Article Snippet: Peptide, recombinant protein , Activated Akt1 , ProQinase , Cat# 1379-0000-2 , .

    Techniques: Tandem Mass Spectroscopy, Phospho-proteomics, Incubation

    Journal: eLife

    Article Title: Inhibition of the Notch signal transducer CSL by Pkc53E-mediated phosphorylation to fend off parasitic immune challenge in Drosophila

    doi: 10.7554/eLife.89582

    Figure Lengend Snippet:

    Article Snippet: Peptide, recombinant protein , Activated Akt1 , ProQinase , Cat# 1379-0000-2 , .

    Techniques: Recombinant, In Vitro, Expressing, Activation Assay, Control, Transfection, Construct, Activity Assay, Clone Assay, Knock-In, Mutagenesis, Knock-Out, Phospho-proteomics, Kinase Assay, Purification, cDNA Synthesis, Reporter Assay, Software, Sequencing