Review



alphascreen igg  (Revvity)


Bioz Verified Symbol Revvity is a verified supplier
Bioz Manufacturer Symbol Revvity manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 91

    Structured Review

    Revvity alphascreen igg
    Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All <t>AlphaScreen</t> signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).
    Alphascreen Igg, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/AlphaScreen+SureFire+HV+IgG+(Protein+A)+Detection+Kit/pmc10290147-213-6-12
    Average 91 stars, based on 15 article reviews
    alphascreen igg - by Bioz Stars, 2026-10
    91/100 stars

    Images

    1) Product Images from "GATS tag system is compatible with biotin labelling methods for protein analysis"

    Article Title: GATS tag system is compatible with biotin labelling methods for protein analysis

    Journal: Scientific Reports

    doi: 10.1038/s41598-023-36858-y

    Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All AlphaScreen signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).
    Figure Legend Snippet: Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All AlphaScreen signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).

    Techniques Used: Bioprocessing, Western Blot, Binding Assay, Control, Synthesized, Produced, In Vitro, Amplified Luminescent Proximity Homogenous Assay, Standard Deviation, Purification

    Broad epitope determination of Ra3, Ra9, and Ra13. ( a ) Diagram representing the GAMA-F fragment for epitope determination. ( b ) Identification of epitope region using A, B, and C GAMA-F fragments. These fragments were fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system. Binding between the fusion protein and Ra3, Ra9, and Ra13 antibodies was detected by AlphaScreen. ( c ) Identification of epitope region using smaller segmented fragments of A, B, and C. ( d ) Diagram representing the lysine residues of the GAMA-F fragment.
    Figure Legend Snippet: Broad epitope determination of Ra3, Ra9, and Ra13. ( a ) Diagram representing the GAMA-F fragment for epitope determination. ( b ) Identification of epitope region using A, B, and C GAMA-F fragments. These fragments were fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system. Binding between the fusion protein and Ra3, Ra9, and Ra13 antibodies was detected by AlphaScreen. ( c ) Identification of epitope region using smaller segmented fragments of A, B, and C. ( d ) Diagram representing the lysine residues of the GAMA-F fragment.

    Techniques Used: Synthesized, Binding Assay, Amplified Luminescent Proximity Homogenous Assay

    The minimal amino acid epitope determination of Ra3. ( a ) Immunoblot analysis of deletion mutants to identify the minimum Ra48 epitope sequence. ( b ) Kinetics assay of the GATS tag and anti-GATS antibody. Anti-GATS antibody was captured on a protein G-immobilized Biacore sensorchip at 1500 RU. Purified FLAG-GST-GATS protein was then injected for 1600 s as analyte. Black lines represent a global fit of a 1:1 interaction model to each kinetic data set. ( c ) Pointing out antibody concentrations in AlphaScreen. The GATS tag was fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system.
    Figure Legend Snippet: The minimal amino acid epitope determination of Ra3. ( a ) Immunoblot analysis of deletion mutants to identify the minimum Ra48 epitope sequence. ( b ) Kinetics assay of the GATS tag and anti-GATS antibody. Anti-GATS antibody was captured on a protein G-immobilized Biacore sensorchip at 1500 RU. Purified FLAG-GST-GATS protein was then injected for 1600 s as analyte. Black lines represent a global fit of a 1:1 interaction model to each kinetic data set. ( c ) Pointing out antibody concentrations in AlphaScreen. The GATS tag was fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system.

    Techniques Used: Western Blot, Sequencing, Purification, Injection, Amplified Luminescent Proximity Homogenous Assay, Synthesized

    Related Articles

    Phospho-proteomics:

    Article Title: The Expression of Cellular Prion Protein, PrPC, Favors pTau Propagation and Blocks NMDAR Signaling in Primary Cortical Neurons
    Article Snippet: .. A total of 10 microliters of each supernatant was placed in white ProxiPlate 384-well microplates, and ERK1/2 phosphorylation was determined using the AlphaScreen ® SureFire ® kit (PerkinElmer) following the instructions of the supplier and using an EnSpire Multimode Plate Reader (PerkinElmer, Waltham, MA, USA). .. Cell signaling was explored using an EnSpire ® Multimode Plate Reader (PerkinElmer) with label-free technology.

    Article Title: Angiotensin AT1 and AT2 receptor heteromer expression in the hemilesioned rat model of Parkinson’s disease that increases with levodopa-induced dyskinesia
    Article Snippet: .. Panels A-C: ERK1/2 phosphorylation was analyzed using an AlphaScreen®SureFire® kit (Perkin Elmer). ..

    Article Title: Intracellular Calcium Levels Determine Differential Modulations of Allosteric Interactions within G Protein-Coupled Receptor Heteromers
    Article Snippet: Fluorescence at 665 nm was analyzed on a PHERAstar Flagship microplate reader equipped with an HTRF optical module (BMG Labtechnologies, Offenburg, Germany). .. ERK 1/2 phosphorylation was determined using the AlphaScreen SureFire kit (Perkin Elmer) following the instructions of the supplier and using an EnSpire Multimode Plate Reader (PerkinElmer, Waltham, MA, USA). ..

    Article Title: Angiotensin AT1 and AT2 receptor heteromer expression in the hemilesioned rat model of Parkinson’s disease that increases with levodopa-induced dyskinesia
    Article Snippet: .. 10 μL of each supernatant were placed in white ProxiPlate 384-well microplates and ERK1/2 phosphorylation was determined using AlphaScreen®SureFire® kit (Perkin Elmer) following the instructions of the supplier and using an EnSpire® Multimode Plate Reader (PerkinElmer, Waltham, MA, USA). .. Dynamic Mass-Redistribution (DMR) label free assays Cell signaling was explored using an EnSpire® Multimode Plate Reader (PerkinElmer, Waltham, MA, USA) by a label-free technology.

    Article Title: Experimental and computational analysis of biased agonism on full-length and a C-terminally truncated adenosine A 2A receptor
    Article Snippet: 10 μl of each cell lysate was transferred to white ProxiPlate 384-well microplates (PerkinElmer; Waltham, MA, USA). .. ERK1/2 phosphorylation was determined using AlphaScreen®SureFire® kit (Perkin Elmer, Waltham, MA, US): 5 μl/well of acceptor beads were added. ..

    Amplified Luminescent Proximity Homogenous Assay:

    Article Title: The Expression of Cellular Prion Protein, PrPC, Favors pTau Propagation and Blocks NMDAR Signaling in Primary Cortical Neurons
    Article Snippet: .. A total of 10 microliters of each supernatant was placed in white ProxiPlate 384-well microplates, and ERK1/2 phosphorylation was determined using the AlphaScreen ® SureFire ® kit (PerkinElmer) following the instructions of the supplier and using an EnSpire Multimode Plate Reader (PerkinElmer, Waltham, MA, USA). .. Cell signaling was explored using an EnSpire ® Multimode Plate Reader (PerkinElmer) with label-free technology.

    Article Title: Angiotensin AT1 and AT2 receptor heteromer expression in the hemilesioned rat model of Parkinson’s disease that increases with levodopa-induced dyskinesia
    Article Snippet: .. Panels A-C: ERK1/2 phosphorylation was analyzed using an AlphaScreen®SureFire® kit (Perkin Elmer). ..

    Article Title: Pharmacological hallmarks of allostery at the M4 muscarinic receptor elucidated through structure and dynamics
    Article Snippet: .. The level of phosphorylated extracellular signal-regulated protein kinase 1/2 (pERK1/2) was detected using the AlphaScreen SureFire Kit (PerkinElmer Life and Analytical Sciences). ..

    Article Title: Intracellular Calcium Levels Determine Differential Modulations of Allosteric Interactions within G Protein-Coupled Receptor Heteromers
    Article Snippet: Fluorescence at 665 nm was analyzed on a PHERAstar Flagship microplate reader equipped with an HTRF optical module (BMG Labtechnologies, Offenburg, Germany). .. ERK 1/2 phosphorylation was determined using the AlphaScreen SureFire kit (Perkin Elmer) following the instructions of the supplier and using an EnSpire Multimode Plate Reader (PerkinElmer, Waltham, MA, USA). ..

    Article Title: Angiotensin AT1 and AT2 receptor heteromer expression in the hemilesioned rat model of Parkinson’s disease that increases with levodopa-induced dyskinesia
    Article Snippet: .. 10 μL of each supernatant were placed in white ProxiPlate 384-well microplates and ERK1/2 phosphorylation was determined using AlphaScreen®SureFire® kit (Perkin Elmer) following the instructions of the supplier and using an EnSpire® Multimode Plate Reader (PerkinElmer, Waltham, MA, USA). .. Dynamic Mass-Redistribution (DMR) label free assays Cell signaling was explored using an EnSpire® Multimode Plate Reader (PerkinElmer, Waltham, MA, USA) by a label-free technology.

    Article Title: Experimental and computational analysis of biased agonism on full-length and a C-terminally truncated adenosine A 2A receptor
    Article Snippet: 10 μl of each cell lysate was transferred to white ProxiPlate 384-well microplates (PerkinElmer; Waltham, MA, USA). .. ERK1/2 phosphorylation was determined using AlphaScreen®SureFire® kit (Perkin Elmer, Waltham, MA, US): 5 μl/well of acceptor beads were added. ..



    Similar Products

    91
    Revvity alphascreen igg
    Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All <t>AlphaScreen</t> signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).
    Alphascreen Igg, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/AlphaScreen+SureFire+HV+IgG+(Protein+A)+Detection+Kit/pmc10290147-213-6-12
    Average 91 stars, based on 1 article reviews
    alphascreen igg - by Bioz Stars, 2026-10
    91/100 stars
      Buy from Supplier

    91
    Revvity alphascreen surefire p akt
    Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All <t>AlphaScreen</t> signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).
    Alphascreen Surefire P Akt, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/AlphaScreen+SureFire+CHK2+(p-Thr68)+Assay+Kit+-+500+Points/pmc10316653-358-10-23
    Average 91 stars, based on 1 article reviews
    alphascreen surefire p akt - by Bioz Stars, 2026-10
    91/100 stars
      Buy from Supplier

    91
    Revvity alphascreen surefire kit
    Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All <t>AlphaScreen</t> signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).
    Alphascreen Surefire Kit, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/AlphaScreen+SureFire+Total+IkB+alpha+Assay+Kit+-+500+Points/pmc10229135-504-14-17
    Average 91 stars, based on 1 article reviews
    alphascreen surefire kit - by Bioz Stars, 2026-10
    91/100 stars
      Buy from Supplier

    91
    Revvity alphascreen surefire perk 1 2

    Alphascreen Surefire Perk 1 2, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/AlphaScreen+SureFire+CHK2+(p-Thr68)+Assay+Kit+-+500+Points/pmc10229135-215-5-13
    Average 91 stars, based on 1 article reviews
    alphascreen surefire perk 1 2 - by Bioz Stars, 2026-10
    91/100 stars
      Buy from Supplier

    91
    Revvity alphascreen surefire erk 1 2

    Alphascreen Surefire Erk 1 2, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/AlphaScreen+SureFire+CHK2+(p-Thr68)+Assay+Kit+-+500+Points/ppr0667419-521-17-24
    Average 91 stars, based on 1 article reviews
    alphascreen surefire erk 1 2 - by Bioz Stars, 2026-10
    91/100 stars
      Buy from Supplier

    91
    Revvity alphascreen general igg protein a detection kit

    Alphascreen General Igg Protein A Detection Kit, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/AlphaScreen+SureFire+HV+IgG+(Protein+A)+Detection+Kit/pmc10019920-163-52-68
    Average 91 stars, based on 1 article reviews
    alphascreen general igg protein a detection kit - by Bioz Stars, 2026-10
    91/100 stars
      Buy from Supplier

    90
    TGR BioSciences alphascreen erk1/2 surefire assay kit

    Alphascreen Erk1/2 Surefire Assay Kit, supplied by TGR BioSciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alphascreen+surefire+kit/erk1+2+assay+kit/pm36550621-80-6-11
    Average 90 stars, based on 1 article reviews
    alphascreen erk1/2 surefire assay kit - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    Image Search Results


    Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All AlphaScreen signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).

    Journal: Scientific Reports

    Article Title: GATS tag system is compatible with biotin labelling methods for protein analysis

    doi: 10.1038/s41598-023-36858-y

    Figure Lengend Snippet: Identification of anti-GAMA rabbit monoclonal antibodies. ( a ) A simplified cellular model of Plasmodium falciparum . ( b ) Domain information on the GAMA protein and the location of GAMA-F. ( c ) Image showing immunoblotting evaluation of the binding of antibodies to GAMA-F and Ripr-F (control) synthesized using a wheat cell-free protein synthesis system. Antibodies are unpurified supernatants produced in Expi293F cells. ( d ) In vitro interaction assay of rabbit monoclonal antibodies clone (Ra) and GAMA-F. Ripr-F is used as control. Antibodies are unpurified supernatants produced in Expi293F cells. All AlphaScreen signals are raw luminescent signals in the AlphaScreen-based biochemical assay. Error bars denote the standard deviation (independent experiments; n = 3). ( e ) Evaluation of antibody specificity with lysates of P. falciparum . Antibodies are produced in Expi293F cells and purified by protein G Sepharose 4 Fast Flow (GE Healthcare).

    Article Snippet: Antibody binding was detected using an AlphaScreen IgG (Protein A) detection kit (Perkin Elmer).

    Techniques: Bioprocessing, Western Blot, Binding Assay, Control, Synthesized, Produced, In Vitro, Amplified Luminescent Proximity Homogenous Assay, Standard Deviation, Purification

    Broad epitope determination of Ra3, Ra9, and Ra13. ( a ) Diagram representing the GAMA-F fragment for epitope determination. ( b ) Identification of epitope region using A, B, and C GAMA-F fragments. These fragments were fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system. Binding between the fusion protein and Ra3, Ra9, and Ra13 antibodies was detected by AlphaScreen. ( c ) Identification of epitope region using smaller segmented fragments of A, B, and C. ( d ) Diagram representing the lysine residues of the GAMA-F fragment.

    Journal: Scientific Reports

    Article Title: GATS tag system is compatible with biotin labelling methods for protein analysis

    doi: 10.1038/s41598-023-36858-y

    Figure Lengend Snippet: Broad epitope determination of Ra3, Ra9, and Ra13. ( a ) Diagram representing the GAMA-F fragment for epitope determination. ( b ) Identification of epitope region using A, B, and C GAMA-F fragments. These fragments were fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system. Binding between the fusion protein and Ra3, Ra9, and Ra13 antibodies was detected by AlphaScreen. ( c ) Identification of epitope region using smaller segmented fragments of A, B, and C. ( d ) Diagram representing the lysine residues of the GAMA-F fragment.

    Article Snippet: Antibody binding was detected using an AlphaScreen IgG (Protein A) detection kit (Perkin Elmer).

    Techniques: Synthesized, Binding Assay, Amplified Luminescent Proximity Homogenous Assay

    The minimal amino acid epitope determination of Ra3. ( a ) Immunoblot analysis of deletion mutants to identify the minimum Ra48 epitope sequence. ( b ) Kinetics assay of the GATS tag and anti-GATS antibody. Anti-GATS antibody was captured on a protein G-immobilized Biacore sensorchip at 1500 RU. Purified FLAG-GST-GATS protein was then injected for 1600 s as analyte. Black lines represent a global fit of a 1:1 interaction model to each kinetic data set. ( c ) Pointing out antibody concentrations in AlphaScreen. The GATS tag was fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system.

    Journal: Scientific Reports

    Article Title: GATS tag system is compatible with biotin labelling methods for protein analysis

    doi: 10.1038/s41598-023-36858-y

    Figure Lengend Snippet: The minimal amino acid epitope determination of Ra3. ( a ) Immunoblot analysis of deletion mutants to identify the minimum Ra48 epitope sequence. ( b ) Kinetics assay of the GATS tag and anti-GATS antibody. Anti-GATS antibody was captured on a protein G-immobilized Biacore sensorchip at 1500 RU. Purified FLAG-GST-GATS protein was then injected for 1600 s as analyte. Black lines represent a global fit of a 1:1 interaction model to each kinetic data set. ( c ) Pointing out antibody concentrations in AlphaScreen. The GATS tag was fused to the N-terminus of GST-TEV-bls protein and synthesized using a wheat germ cell-free system.

    Article Snippet: Antibody binding was detected using an AlphaScreen IgG (Protein A) detection kit (Perkin Elmer).

    Techniques: Western Blot, Sequencing, Purification, Injection, Amplified Luminescent Proximity Homogenous Assay, Synthesized

    Journal: eLife

    Article Title: Pharmacological hallmarks of allostery at the M4 muscarinic receptor elucidated through structure and dynamics

    doi: 10.7554/eLife.83477

    Figure Lengend Snippet:

    Article Snippet: Commercial assay or kit , AlphaScreen SureFire pERK 1/2 (Thr202/Tyr204) Assay Kits , PerkinElmer , , .

    Techniques: Purification, Expressing, Plasmid Preparation, Recombinant, Dominant Negative Mutation, Amplified Luminescent Proximity Homogenous Assay, Software