ligand binding module in sigmaplot 11 software (SYSTAT)
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ligand binding module in sigmaplot 11 software
Ligand Binding Module In Sigmaplot 11 Software, supplied by SYSTAT, 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/ligand+binding+module+sigmaplot/the+ligand+binding+macro+of+the+sigmaplot++version+11++program/pm23318174-51-4-9
Average 90 stars, based on 1 article reviews
Ligand Binding Module In Sigmaplot 11 Software, supplied by SYSTAT, 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/ligand+binding+module+sigmaplot/the+ligand+binding+macro+of+the+sigmaplot++version+11++program/pm23318174-51-4-9
Average 90 stars, based on 1 article reviews
ligand binding module in sigmaplot 11 software - by Bioz Stars,
2026-11
90/100 stars
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other:Article Title: A Novel Cyclic Adenosine Monophosphate-Responsive Luciferase Reporter Incorporating a Nonpalindromic Cyclic Adenosine Monophosphate Response Element Provides Optimal Performance for Use in G Protein-Coupled Receptor Drug Discovery Efforts Article Snippet: Data that are presented graphically were plotted using the ligand-binding module of Article Title: Novel mutations and mutation combinations of ryanodine receptor in a chlorantraniliprole resistant population of Plutella xylostella (L.) Article Snippet: Then the FP intensities and the logarithm transformed membrane protein concentrations were subjected to the ligand binding module of Article Title: Substrate Specificity and Function of the Pheromone Receptor AinR in Vibrio fischeri ES114 Article Snippet: EC 50 s were determined with the Article Title: Identification of a Receptor Subunit and Putative Ligand-Binding Residues Involved in the Bacillus megaterium QM B1551 Spore Germination Response to Glucose Article Snippet: Apparent K m and V max values were subsequently determined using the ligand-binding macro of the Ligand Binding Assay:Article Title: Pluripotency transcription factor Sox2 is strongly adsorbed by heparin but requires a protein transduction domain for cell internalization. Article Snippet: 0006-291X/$ see front matter 2012 Elsevier Inc. A http://dx.doi.org/10.1016/j.bbrc.2012.11.016 ⇑ Corresponding author at: Department of Che University, 381 North-South Mall, Stanford, CA 94305 E-mail address: jswartz@stanford.edu (J.R. Swartz) 1 Present Address: Biogen Idec Inc., 5000 Davis Driv 27709, USA.. The binding of protein transduction domain (PTD)-conjugated proteins to heparan sulfate is an important step in cellular internalization of macromolecules.. Here, we studied the pluripotency transcription factor Sox2, with or without the nonaarginine (R9) PTD. Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Ligand Binding Module of Sigmaplot (Systat Software Inc., UK). .. Binding specificity was determined by incubating plasma samples (diluted 1:15) with 0.2 nM 3[H]E2 with or without cold competitors for 60 min at 4 C. The concentration of cold competitor that displaced 50% of radioligand bound (EC50), the relative binding affinity (RBA) and the concentration of radioinert competitor which bound 50% of specific bound in absence of radioligand (Ki) were calculated using the ligand binding module of Article Title: Cytokinin Perception in Ancient Plants beyond Angiospermae Article Snippet: .. The competition curves were generated using the simple Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: .. The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Software:Article Title: Pluripotency transcription factor Sox2 is strongly adsorbed by heparin but requires a protein transduction domain for cell internalization. Article Snippet: 0006-291X/$ see front matter 2012 Elsevier Inc. A http://dx.doi.org/10.1016/j.bbrc.2012.11.016 ⇑ Corresponding author at: Department of Che University, 381 North-South Mall, Stanford, CA 94305 E-mail address: jswartz@stanford.edu (J.R. Swartz) 1 Present Address: Biogen Idec Inc., 5000 Davis Driv 27709, USA.. The binding of protein transduction domain (PTD)-conjugated proteins to heparan sulfate is an important step in cellular internalization of macromolecules.. Here, we studied the pluripotency transcription factor Sox2, with or without the nonaarginine (R9) PTD. Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Ligand Binding Module of Sigmaplot (Systat Software Inc., UK). .. Binding specificity was determined by incubating plasma samples (diluted 1:15) with 0.2 nM 3[H]E2 with or without cold competitors for 60 min at 4 C. The concentration of cold competitor that displaced 50% of radioligand bound (EC50), the relative binding affinity (RBA) and the concentration of radioinert competitor which bound 50% of specific bound in absence of radioligand (Ki) were calculated using the ligand binding module of Binding Assay:Article Title: Pluripotency transcription factor Sox2 is strongly adsorbed by heparin but requires a protein transduction domain for cell internalization. Article Snippet: 0006-291X/$ see front matter 2012 Elsevier Inc. A http://dx.doi.org/10.1016/j.bbrc.2012.11.016 ⇑ Corresponding author at: Department of Che University, 381 North-South Mall, Stanford, CA 94305 E-mail address: jswartz@stanford.edu (J.R. Swartz) 1 Present Address: Biogen Idec Inc., 5000 Davis Driv 27709, USA.. The binding of protein transduction domain (PTD)-conjugated proteins to heparan sulfate is an important step in cellular internalization of macromolecules.. Here, we studied the pluripotency transcription factor Sox2, with or without the nonaarginine (R9) PTD. Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Ligand Binding Module of Sigmaplot (Systat Software Inc., UK). .. Binding specificity was determined by incubating plasma samples (diluted 1:15) with 0.2 nM 3[H]E2 with or without cold competitors for 60 min at 4 C. The concentration of cold competitor that displaced 50% of radioligand bound (EC50), the relative binding affinity (RBA) and the concentration of radioinert competitor which bound 50% of specific bound in absence of radioligand (Ki) were calculated using the ligand binding module of Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: .. The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Concentration Assay:Article Title: Pluripotency transcription factor Sox2 is strongly adsorbed by heparin but requires a protein transduction domain for cell internalization. Article Snippet: 0006-291X/$ see front matter 2012 Elsevier Inc. A http://dx.doi.org/10.1016/j.bbrc.2012.11.016 ⇑ Corresponding author at: Department of Che University, 381 North-South Mall, Stanford, CA 94305 E-mail address: jswartz@stanford.edu (J.R. Swartz) 1 Present Address: Biogen Idec Inc., 5000 Davis Driv 27709, USA.. The binding of protein transduction domain (PTD)-conjugated proteins to heparan sulfate is an important step in cellular internalization of macromolecules.. Here, we studied the pluripotency transcription factor Sox2, with or without the nonaarginine (R9) PTD. Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Ligand Binding Module of Sigmaplot (Systat Software Inc., UK). .. Binding specificity was determined by incubating plasma samples (diluted 1:15) with 0.2 nM 3[H]E2 with or without cold competitors for 60 min at 4 C. The concentration of cold competitor that displaced 50% of radioligand bound (EC50), the relative binding affinity (RBA) and the concentration of radioinert competitor which bound 50% of specific bound in absence of radioligand (Ki) were calculated using the ligand binding module of Clinical Proteomics:Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Ligand Binding Module of Sigmaplot (Systat Software Inc., UK). .. Binding specificity was determined by incubating plasma samples (diluted 1:15) with 0.2 nM 3[H]E2 with or without cold competitors for 60 min at 4 C. The concentration of cold competitor that displaced 50% of radioligand bound (EC50), the relative binding affinity (RBA) and the concentration of radioinert competitor which bound 50% of specific bound in absence of radioligand (Ki) were calculated using the ligand binding module of Article Title: Tilapia male urinary pheromone stimulates female reproductive axis. Article Snippet: .. The binding affinity (Kd) and maximum binding sites capacity (Bmax) for E2 were determined by incubating plasma diluted 1:10 (v/v) with increasing concentrations (0.2–60 nM) of 3[H]E2 with or without 1.5 mM ‘cold’ E2 for 2 h at 4 C. The dissociation constant (Kd) and binding capacity (Bmax) were calculated by Scatchard plot with the Generated:Article Title: Cytokinin Perception in Ancient Plants beyond Angiospermae Article Snippet: .. The competition curves were generated using the simple |