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pt3 myr akt  (Addgene inc)


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    Structured Review

    Addgene inc pt3 myr akt
    Pt3 Myr Akt, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 68 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/myr/pT3-myr-AKT-HA+(Plasmid+%2331789)/pm41928626-184-4-5
    Average 94 stars, based on 68 article reviews
    pt3 myr akt - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Generated:

    Article Title: Localized heterochrony integrates overgrowth potential of oncogenic clones
    Article Snippet: Plasmid pminiTol2 ( Addgene #31829 ) was used as backbone vector and transgene cassettes ubi:eGFP , ubi:akt1 E18K , ubi:myr-p110 and hsp70:akt1 E18K were inserted into the multiple cloning site. .. Transgene cassettes were generated by inserting eGFP from pME-eGFP ( Tol2kit #383 ), murine myr-p110 from Myr-(iSH2-p85)-p110alpha-Myc ( Addgene #1410 ) or zebrafish akt1 E18K together with the SV40 late polyadenylation signal (SV40pA) downstream of the ubi or hsp70 promoter into pENTR5'_ubi ( Addgene #27320 ) or p5E-hsp70I ( Tol2kit #222 ), respectively. .. The full-length coding sequence of zebrafish akt1 was amplified from 24 h post fertilization cDNA and the E18K mutation was introduced using QuickChange Site-Directed mutagenesis (Agilent).

    Article Title: Localized heterochrony integrates overgrowth potential of oncogenic clones
    Article Snippet: The following plasmids were constructed for injection: pmTol2-ubi:eGFP (control construct), pmTol2-ubi:akt 1E18K -ubi:eGPF, pmTol2-ubi:myr-p110-ubi:eGPF. pminiTol2 (Addgene #31829) was used as backbone vector and transgene cassettes ( ubi:eGFP, ubi:akt1 E18K and ubi:myr-p110 ) were inserted into the multiple cloning site. .. Transgene cassettes were generated by inserting eGFP from pME-eGFP (Tol2kit #383), murine myr-p110 from Myr-(iSH2-p85)-p110alpha-Myc (Addgene #1410) or zebrafish akt1 E18K together with the SV40 late polyadenylation signal (SV40pA) downstream of the ubi promoter into pENTR5’ubi (Addgene #27320). .. The full length coding sequence of zebrafish akt1 was amplified from 24 hours post fertilization cDNA and the E18K mutation was introduced using QuickChange Site-Directed mutagenesis (Agilent).

    Article Title: Synapses in oligodendrocyte precursor cells are dynamic and contribute to Ca 2+ activity
    Article Snippet: .. We generated pME_ATG-PSD-95-GFP-TAA and p3E_p2A-PSD-95-GFP-TGA-polyA. pME_myrGFP and pME_myrTagRFP-T were generated using PCR and BP reaction, using Fyn myristoylation and palmitoylation domain. pGP-CMV-GCaMP6s (Addgene 40753) was used as a template and 3 primers were used in a Q5 PCR (15 cycles at 71° C and 20 cycles at 72° C) to amplify GCaMP6s and add Kozak sequence, myr (Fyn myristoylation and palmitoylation domain), attB1, and attB2 sequences. ..

    Isolation:

    Article Title: Color Processing in the Early Visual System of Drosophila.
    Article Snippet: .. For LexAop-twich-2c a NotI/XbaI fragment including Twitch-2C DNA was isolated from pUAST-Twich-2c (see above) and cloned into pJFRC19-13XLexAop2-IVS-myr::GFP (kindly provided by Gerald Rubin, Addgene plasmid #26224) by exchanging myr::GFP. rh3, rh4, promoter regions were amplified by standard PCR from pCaST-rh3/4-norpA plasmids (kindly provided by Chi-Hon Lee) adding 5‘-end AatII- and 3‘-end NgoMIV-restriction sites. .. The resulting AatII/NgoMIV fragment was cloned into pBPnLsLexA::GADfluw (kindly provided by Gerald Rubin, Addgene plasmid #26232).

    Clone Assay:

    Article Title: Color Processing in the Early Visual System of Drosophila.
    Article Snippet: .. For LexAop-twich-2c a NotI/XbaI fragment including Twitch-2C DNA was isolated from pUAST-Twich-2c (see above) and cloned into pJFRC19-13XLexAop2-IVS-myr::GFP (kindly provided by Gerald Rubin, Addgene plasmid #26224) by exchanging myr::GFP. rh3, rh4, promoter regions were amplified by standard PCR from pCaST-rh3/4-norpA plasmids (kindly provided by Chi-Hon Lee) adding 5‘-end AatII- and 3‘-end NgoMIV-restriction sites. .. The resulting AatII/NgoMIV fragment was cloned into pBPnLsLexA::GADfluw (kindly provided by Gerald Rubin, Addgene plasmid #26232).

    Plasmid Preparation:

    Article Title: Color Processing in the Early Visual System of Drosophila.
    Article Snippet: .. For LexAop-twich-2c a NotI/XbaI fragment including Twitch-2C DNA was isolated from pUAST-Twich-2c (see above) and cloned into pJFRC19-13XLexAop2-IVS-myr::GFP (kindly provided by Gerald Rubin, Addgene plasmid #26224) by exchanging myr::GFP. rh3, rh4, promoter regions were amplified by standard PCR from pCaST-rh3/4-norpA plasmids (kindly provided by Chi-Hon Lee) adding 5‘-end AatII- and 3‘-end NgoMIV-restriction sites. .. The resulting AatII/NgoMIV fragment was cloned into pBPnLsLexA::GADfluw (kindly provided by Gerald Rubin, Addgene plasmid #26232).

    Article Title: VGLUT modulates sex differences in dopamine neuron vulnerability to age-related neurodegeneration
    Article Snippet: This construct was introduced into the attP40 site on chromosome II by phiC31 injection (Genetivision, Houston, TX). .. The UAS>B3RT-STOP-B3RT-Luciferase strain was created by replacement of the myr::RFP sequence in pJFRC160 (Addgene plasmid #32139) with firefly luciferase. .. This modified construct was introduced into the attP2 site on chromosome III by phiC31 injection (Genetivision).

    Amplification:

    Article Title: Color Processing in the Early Visual System of Drosophila.
    Article Snippet: .. For LexAop-twich-2c a NotI/XbaI fragment including Twitch-2C DNA was isolated from pUAST-Twich-2c (see above) and cloned into pJFRC19-13XLexAop2-IVS-myr::GFP (kindly provided by Gerald Rubin, Addgene plasmid #26224) by exchanging myr::GFP. rh3, rh4, promoter regions were amplified by standard PCR from pCaST-rh3/4-norpA plasmids (kindly provided by Chi-Hon Lee) adding 5‘-end AatII- and 3‘-end NgoMIV-restriction sites. .. The resulting AatII/NgoMIV fragment was cloned into pBPnLsLexA::GADfluw (kindly provided by Gerald Rubin, Addgene plasmid #26232).

    Polymerase Chain Reaction:

    Article Title: Color Processing in the Early Visual System of Drosophila.
    Article Snippet: .. For LexAop-twich-2c a NotI/XbaI fragment including Twitch-2C DNA was isolated from pUAST-Twich-2c (see above) and cloned into pJFRC19-13XLexAop2-IVS-myr::GFP (kindly provided by Gerald Rubin, Addgene plasmid #26224) by exchanging myr::GFP. rh3, rh4, promoter regions were amplified by standard PCR from pCaST-rh3/4-norpA plasmids (kindly provided by Chi-Hon Lee) adding 5‘-end AatII- and 3‘-end NgoMIV-restriction sites. .. The resulting AatII/NgoMIV fragment was cloned into pBPnLsLexA::GADfluw (kindly provided by Gerald Rubin, Addgene plasmid #26232).

    Article Title: Synapses in oligodendrocyte precursor cells are dynamic and contribute to Ca 2+ activity
    Article Snippet: .. We generated pME_ATG-PSD-95-GFP-TAA and p3E_p2A-PSD-95-GFP-TGA-polyA. pME_myrGFP and pME_myrTagRFP-T were generated using PCR and BP reaction, using Fyn myristoylation and palmitoylation domain. pGP-CMV-GCaMP6s (Addgene 40753) was used as a template and 3 primers were used in a Q5 PCR (15 cycles at 71° C and 20 cycles at 72° C) to amplify GCaMP6s and add Kozak sequence, myr (Fyn myristoylation and palmitoylation domain), attB1, and attB2 sequences. ..

    other:

    Article Title: Color Processing in the Early Visual System of Drosophila.
    Article Snippet: The resulting AatII/NgoMIV fragment was cloned into pBPnLsLexA::GADfluw (kindly provided by Gerald Rubin, Addgene plasmid #26232).

    Sequencing:

    Article Title: VGLUT modulates sex differences in dopamine neuron vulnerability to age-related neurodegeneration
    Article Snippet: This construct was introduced into the attP40 site on chromosome II by phiC31 injection (Genetivision, Houston, TX). .. The UAS>B3RT-STOP-B3RT-Luciferase strain was created by replacement of the myr::RFP sequence in pJFRC160 (Addgene plasmid #32139) with firefly luciferase. .. This modified construct was introduced into the attP2 site on chromosome III by phiC31 injection (Genetivision).

    Article Title: Synapses in oligodendrocyte precursor cells are dynamic and contribute to Ca 2+ activity
    Article Snippet: .. We generated pME_ATG-PSD-95-GFP-TAA and p3E_p2A-PSD-95-GFP-TGA-polyA. pME_myrGFP and pME_myrTagRFP-T were generated using PCR and BP reaction, using Fyn myristoylation and palmitoylation domain. pGP-CMV-GCaMP6s (Addgene 40753) was used as a template and 3 primers were used in a Q5 PCR (15 cycles at 71° C and 20 cycles at 72° C) to amplify GCaMP6s and add Kozak sequence, myr (Fyn myristoylation and palmitoylation domain), attB1, and attB2 sequences. ..

    Luciferase:

    Article Title: VGLUT modulates sex differences in dopamine neuron vulnerability to age-related neurodegeneration
    Article Snippet: This construct was introduced into the attP40 site on chromosome II by phiC31 injection (Genetivision, Houston, TX). .. The UAS>B3RT-STOP-B3RT-Luciferase strain was created by replacement of the myr::RFP sequence in pJFRC160 (Addgene plasmid #32139) with firefly luciferase. .. This modified construct was introduced into the attP2 site on chromosome III by phiC31 injection (Genetivision).



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    Image Search Results


    ( A ) Schematic of XL-MS workflow. ( B ) XL-based interactome of synaptic ribosomes. Synaptic annotation is based on SynGO (dataset version 20231201). ( C ) Protein domain-level crosslink map between RPL35 and CaMKIIα. Domain classification based on . ( D ) Structural model of CaMKIIα binding to the ribosome. Most CaMKIIα–RPL35 crosslinks satisfy distance constraints (green), with remaining links accommodated by CaMKIIα linker flexibility (yellow). ( E ) Detection of newly-synthesized proteins in dendrites and synapses from control (untreated) neurons or neurons treated with 10 μM KN-93 or myr-AIP for 30 min. Nascent proteins were labeled with puromycin (5 min) in the absence or presence of the protein synthesis inhibitor anisomycin (see Methods). Scale bar, 5 µm. ( F ) Quantification of puromycin signal in postsynaptic regions of the apical dendritic arbor from control and treated neurons. Error bars show mean ± SEM. **p<0.01; ****p<0.0001, Brown-Forsythe and Welch’s ANOVA, Dunnett’s multiple comparisons test; n=58-64 neurons from 3 independent cultures.

    Journal: bioRxiv

    Article Title: Direct interaction of ribosomes with postsynaptic proteins gives rise to a privileged local synaptic translatome

    doi: 10.64898/2026.02.27.708433

    Figure Lengend Snippet: ( A ) Schematic of XL-MS workflow. ( B ) XL-based interactome of synaptic ribosomes. Synaptic annotation is based on SynGO (dataset version 20231201). ( C ) Protein domain-level crosslink map between RPL35 and CaMKIIα. Domain classification based on . ( D ) Structural model of CaMKIIα binding to the ribosome. Most CaMKIIα–RPL35 crosslinks satisfy distance constraints (green), with remaining links accommodated by CaMKIIα linker flexibility (yellow). ( E ) Detection of newly-synthesized proteins in dendrites and synapses from control (untreated) neurons or neurons treated with 10 μM KN-93 or myr-AIP for 30 min. Nascent proteins were labeled with puromycin (5 min) in the absence or presence of the protein synthesis inhibitor anisomycin (see Methods). Scale bar, 5 µm. ( F ) Quantification of puromycin signal in postsynaptic regions of the apical dendritic arbor from control and treated neurons. Error bars show mean ± SEM. **p<0.01; ****p<0.0001, Brown-Forsythe and Welch’s ANOVA, Dunnett’s multiple comparisons test; n=58-64 neurons from 3 independent cultures.

    Article Snippet: DIV 18-19 hippocampal neurons were treated with either 10 μM KN-93 (Tocris, #5215) or 10 μM myr-AIP (Tocris, #5959) for 30 min at 37°C, or left untreated.

    Techniques: Structural Proteomics, Binding Assay, Synthesized, Control, Labeling