Structured Review

Millipore rabbit antibody against d1r
Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on <t>D1R–GluN1</t> interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of <t>D1R–GluN1</t> interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
Rabbit Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit antibody against d1r/product/Millipore
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
rabbit antibody against d1r - by Bioz Stars, 2024-09
86/100 stars

Images

1) Product Images from "Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats"

Article Title: Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats

Journal: Drug Design, Development and Therapy

doi: 10.2147/DDDT.S93487

Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
Figure Legend Snippet: Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.

Techniques Used: Injection, Immunoprecipitation, Western Blot

Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.
Figure Legend Snippet: Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

Techniques Used: Expressing, Western Blot


Structured Review

Millipore rabbit primary antibody against d1r
Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on <t>D1R–GluN1</t> interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of <t>D1R–GluN1</t> interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
Rabbit Primary Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit primary antibody against d1r/product/Millipore
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
rabbit primary antibody against d1r - by Bioz Stars, 2024-09
86/100 stars

Images

1) Product Images from "Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats"

Article Title: Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats

Journal: Drug Design, Development and Therapy

doi: 10.2147/DDDT.S93487

Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
Figure Legend Snippet: Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.

Techniques Used: Injection, Immunoprecipitation, Western Blot

Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.
Figure Legend Snippet: Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

Techniques Used: Expressing, Western Blot


Structured Review

Abcam rabbit antibody against d1r
Rabbit Antibody Against D1r, supplied by Abcam, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit antibody against d1r/product/Abcam
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
rabbit antibody against d1r - by Bioz Stars, 2024-09
86/100 stars

Images


Structured Review

Abcam rabbit antibody against d1r
Rabbit Antibody Against D1r, supplied by Abcam, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit antibody against d1r/product/Abcam
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
rabbit antibody against d1r - by Bioz Stars, 2024-09
86/100 stars

Images

rabbit polyclonal antibodies against da receptors d1r  (Millipore)

 
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Millipore rabbit polyclonal antibodies against da receptors d1r
    Rabbit Polyclonal Antibodies Against Da Receptors D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibodies against da receptors d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal antibodies against da receptors d1r - by Bioz Stars, 2024-09
    86/100 stars

    Images


    Structured Review

    Millipore rabbit antibody against d1r
    Rabbit Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars

    Images


    Structured Review

    Millipore rabbit primary antibody against d1r
    Rabbit Primary Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit primary antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit primary antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars

    Images


    Structured Review

    Millipore rabbit polyclonal antibody against d1r
    Rabbit Polyclonal Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars

    Images


    Structured Review

    Millipore rabbit polyclonal antibody against d1r
    Antagonizing <t>D1-receptor</t> activation in the primary motor cortex of dyskinetic animals disrupts cortical resonance and alleviates dyskinesia. A, Immunohistochemical analysis of dopaminergic markers comparing intact and lesioned MI at the time of peak dyskinesia. Left, Staining of TH-positive dopaminergic axons and terminals was markedly reduced in the lesioned hemisphere. Middle, <t>D1R</t> density in the lesioned hemisphere was unaltered after dopaminergic afferent denervation. Right, Expression of the immediate early gene c-fos after levodopa administration was relatively increased on the lesioned side. B, Topical application of the D1R antagonist SCH23390 to the cortical surface disrupts 80 Hz cortical resonant oscillation and alleviates dyskinetic symptoms. Left, Example of spectrogram from LFP recording in MI, power spectrum normalized to pre-levodopa baseline; D1R-antagonist injection denoted by black bar and faded colors. Dyskinesia score is shown at the bottom (red, rotations; yellow, limbic; turquoise, axial; purple, orolingual). C, Summary of all experiments (n = 11) showing γ80 oscillations (top) and dyskinetic symptoms (bottom) following topical application of SCH23390 (red) or saline (blue), respectively (γ80 power expressed relative to the pink noise background). Note the parallel decline in the power of the resonant LFP oscillation and the dyskinesia score in all experiments (traces during the period of drug application are linearly interpolated). Right, Average data from all experiments showing significant differences between D1R-antagonist vs vehicle treatment before (darker colors) and after topical application. Error bars denote SEM. *p < 0.05. D, Characterization of the relationship between γ80 and severity of dyskinesia during the early dyskinetic phase (first 40 min following levodopa injection) and the cessation of dyskinesia following topical application of SCH23390. Each panel represents a single experiment (n = 5 rats) and displays the dyskinesia score as a function of cortical γ80 power (each symbol denotes average over a 1 min period: filled, early dyskinetic phase; open, cessation of dyskinesia following SCH23390). The relationships were well fitted with sigmoid functions (average goodness-of-fit, R2 = 0.72 ± 0.22). Notably, a similar relation between γ80 power and the severity of dyskinesia is evident during the early phase of dyskinesia and following pharmacological γ80 suppression.
    Rabbit Polyclonal Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars

    Images

    1) Product Images from "Levodopa-Induced Dyskinesia Is Strongly Associated with Resonant Cortical Oscillations"

    Article Title: Levodopa-Induced Dyskinesia Is Strongly Associated with Resonant Cortical Oscillations

    Journal: The Journal of Neuroscience

    doi: 10.1523/JNEUROSCI.3047-12.2012

    Antagonizing D1-receptor activation in the primary motor cortex of dyskinetic animals disrupts cortical resonance and alleviates dyskinesia. A, Immunohistochemical analysis of dopaminergic markers comparing intact and lesioned MI at the time of peak dyskinesia. Left, Staining of TH-positive dopaminergic axons and terminals was markedly reduced in the lesioned hemisphere. Middle, D1R density in the lesioned hemisphere was unaltered after dopaminergic afferent denervation. Right, Expression of the immediate early gene c-fos after levodopa administration was relatively increased on the lesioned side. B, Topical application of the D1R antagonist SCH23390 to the cortical surface disrupts 80 Hz cortical resonant oscillation and alleviates dyskinetic symptoms. Left, Example of spectrogram from LFP recording in MI, power spectrum normalized to pre-levodopa baseline; D1R-antagonist injection denoted by black bar and faded colors. Dyskinesia score is shown at the bottom (red, rotations; yellow, limbic; turquoise, axial; purple, orolingual). C, Summary of all experiments (n = 11) showing γ80 oscillations (top) and dyskinetic symptoms (bottom) following topical application of SCH23390 (red) or saline (blue), respectively (γ80 power expressed relative to the pink noise background). Note the parallel decline in the power of the resonant LFP oscillation and the dyskinesia score in all experiments (traces during the period of drug application are linearly interpolated). Right, Average data from all experiments showing significant differences between D1R-antagonist vs vehicle treatment before (darker colors) and after topical application. Error bars denote SEM. *p < 0.05. D, Characterization of the relationship between γ80 and severity of dyskinesia during the early dyskinetic phase (first 40 min following levodopa injection) and the cessation of dyskinesia following topical application of SCH23390. Each panel represents a single experiment (n = 5 rats) and displays the dyskinesia score as a function of cortical γ80 power (each symbol denotes average over a 1 min period: filled, early dyskinetic phase; open, cessation of dyskinesia following SCH23390). The relationships were well fitted with sigmoid functions (average goodness-of-fit, R2 = 0.72 ± 0.22). Notably, a similar relation between γ80 power and the severity of dyskinesia is evident during the early phase of dyskinesia and following pharmacological γ80 suppression.
    Figure Legend Snippet: Antagonizing D1-receptor activation in the primary motor cortex of dyskinetic animals disrupts cortical resonance and alleviates dyskinesia. A, Immunohistochemical analysis of dopaminergic markers comparing intact and lesioned MI at the time of peak dyskinesia. Left, Staining of TH-positive dopaminergic axons and terminals was markedly reduced in the lesioned hemisphere. Middle, D1R density in the lesioned hemisphere was unaltered after dopaminergic afferent denervation. Right, Expression of the immediate early gene c-fos after levodopa administration was relatively increased on the lesioned side. B, Topical application of the D1R antagonist SCH23390 to the cortical surface disrupts 80 Hz cortical resonant oscillation and alleviates dyskinetic symptoms. Left, Example of spectrogram from LFP recording in MI, power spectrum normalized to pre-levodopa baseline; D1R-antagonist injection denoted by black bar and faded colors. Dyskinesia score is shown at the bottom (red, rotations; yellow, limbic; turquoise, axial; purple, orolingual). C, Summary of all experiments (n = 11) showing γ80 oscillations (top) and dyskinetic symptoms (bottom) following topical application of SCH23390 (red) or saline (blue), respectively (γ80 power expressed relative to the pink noise background). Note the parallel decline in the power of the resonant LFP oscillation and the dyskinesia score in all experiments (traces during the period of drug application are linearly interpolated). Right, Average data from all experiments showing significant differences between D1R-antagonist vs vehicle treatment before (darker colors) and after topical application. Error bars denote SEM. *p < 0.05. D, Characterization of the relationship between γ80 and severity of dyskinesia during the early dyskinetic phase (first 40 min following levodopa injection) and the cessation of dyskinesia following topical application of SCH23390. Each panel represents a single experiment (n = 5 rats) and displays the dyskinesia score as a function of cortical γ80 power (each symbol denotes average over a 1 min period: filled, early dyskinetic phase; open, cessation of dyskinesia following SCH23390). The relationships were well fitted with sigmoid functions (average goodness-of-fit, R2 = 0.72 ± 0.22). Notably, a similar relation between γ80 power and the severity of dyskinesia is evident during the early phase of dyskinesia and following pharmacological γ80 suppression.

    Techniques Used: Activation Assay, Immunohistochemical staining, Staining, Expressing, Injection


    Structured Review

    Millipore rabbit polyclonal antibody against d1r
    Antagonizing <t>D1-receptor</t> activation in the primary motor cortex of dyskinetic animals disrupts cortical resonance and alleviates dyskinesia. A, Immunohistochemical analysis of dopaminergic markers comparing intact and lesioned MI at the time of peak dyskinesia. Left, Staining of TH-positive dopaminergic axons and terminals was markedly reduced in the lesioned hemisphere. Middle, <t>D1R</t> density in the lesioned hemisphere was unaltered after dopaminergic afferent denervation. Right, Expression of the immediate early gene c-fos after levodopa administration was relatively increased on the lesioned side. B, Topical application of the D1R antagonist SCH23390 to the cortical surface disrupts 80 Hz cortical resonant oscillation and alleviates dyskinetic symptoms. Left, Example of spectrogram from LFP recording in MI, power spectrum normalized to pre-levodopa baseline; D1R-antagonist injection denoted by black bar and faded colors. Dyskinesia score is shown at the bottom (red, rotations; yellow, limbic; turquoise, axial; purple, orolingual). C, Summary of all experiments (n = 11) showing γ80 oscillations (top) and dyskinetic symptoms (bottom) following topical application of SCH23390 (red) or saline (blue), respectively (γ80 power expressed relative to the pink noise background). Note the parallel decline in the power of the resonant LFP oscillation and the dyskinesia score in all experiments (traces during the period of drug application are linearly interpolated). Right, Average data from all experiments showing significant differences between D1R-antagonist vs vehicle treatment before (darker colors) and after topical application. Error bars denote SEM. *p < 0.05. D, Characterization of the relationship between γ80 and severity of dyskinesia during the early dyskinetic phase (first 40 min following levodopa injection) and the cessation of dyskinesia following topical application of SCH23390. Each panel represents a single experiment (n = 5 rats) and displays the dyskinesia score as a function of cortical γ80 power (each symbol denotes average over a 1 min period: filled, early dyskinetic phase; open, cessation of dyskinesia following SCH23390). The relationships were well fitted with sigmoid functions (average goodness-of-fit, R2 = 0.72 ± 0.22). Notably, a similar relation between γ80 power and the severity of dyskinesia is evident during the early phase of dyskinesia and following pharmacological γ80 suppression.
    Rabbit Polyclonal Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars

    Images

    1) Product Images from "Levodopa-Induced Dyskinesia Is Strongly Associated with Resonant Cortical Oscillations"

    Article Title: Levodopa-Induced Dyskinesia Is Strongly Associated with Resonant Cortical Oscillations

    Journal: The Journal of Neuroscience

    doi: 10.1523/JNEUROSCI.3047-12.2012

    Antagonizing D1-receptor activation in the primary motor cortex of dyskinetic animals disrupts cortical resonance and alleviates dyskinesia. A, Immunohistochemical analysis of dopaminergic markers comparing intact and lesioned MI at the time of peak dyskinesia. Left, Staining of TH-positive dopaminergic axons and terminals was markedly reduced in the lesioned hemisphere. Middle, D1R density in the lesioned hemisphere was unaltered after dopaminergic afferent denervation. Right, Expression of the immediate early gene c-fos after levodopa administration was relatively increased on the lesioned side. B, Topical application of the D1R antagonist SCH23390 to the cortical surface disrupts 80 Hz cortical resonant oscillation and alleviates dyskinetic symptoms. Left, Example of spectrogram from LFP recording in MI, power spectrum normalized to pre-levodopa baseline; D1R-antagonist injection denoted by black bar and faded colors. Dyskinesia score is shown at the bottom (red, rotations; yellow, limbic; turquoise, axial; purple, orolingual). C, Summary of all experiments (n = 11) showing γ80 oscillations (top) and dyskinetic symptoms (bottom) following topical application of SCH23390 (red) or saline (blue), respectively (γ80 power expressed relative to the pink noise background). Note the parallel decline in the power of the resonant LFP oscillation and the dyskinesia score in all experiments (traces during the period of drug application are linearly interpolated). Right, Average data from all experiments showing significant differences between D1R-antagonist vs vehicle treatment before (darker colors) and after topical application. Error bars denote SEM. *p < 0.05. D, Characterization of the relationship between γ80 and severity of dyskinesia during the early dyskinetic phase (first 40 min following levodopa injection) and the cessation of dyskinesia following topical application of SCH23390. Each panel represents a single experiment (n = 5 rats) and displays the dyskinesia score as a function of cortical γ80 power (each symbol denotes average over a 1 min period: filled, early dyskinetic phase; open, cessation of dyskinesia following SCH23390). The relationships were well fitted with sigmoid functions (average goodness-of-fit, R2 = 0.72 ± 0.22). Notably, a similar relation between γ80 power and the severity of dyskinesia is evident during the early phase of dyskinesia and following pharmacological γ80 suppression.
    Figure Legend Snippet: Antagonizing D1-receptor activation in the primary motor cortex of dyskinetic animals disrupts cortical resonance and alleviates dyskinesia. A, Immunohistochemical analysis of dopaminergic markers comparing intact and lesioned MI at the time of peak dyskinesia. Left, Staining of TH-positive dopaminergic axons and terminals was markedly reduced in the lesioned hemisphere. Middle, D1R density in the lesioned hemisphere was unaltered after dopaminergic afferent denervation. Right, Expression of the immediate early gene c-fos after levodopa administration was relatively increased on the lesioned side. B, Topical application of the D1R antagonist SCH23390 to the cortical surface disrupts 80 Hz cortical resonant oscillation and alleviates dyskinetic symptoms. Left, Example of spectrogram from LFP recording in MI, power spectrum normalized to pre-levodopa baseline; D1R-antagonist injection denoted by black bar and faded colors. Dyskinesia score is shown at the bottom (red, rotations; yellow, limbic; turquoise, axial; purple, orolingual). C, Summary of all experiments (n = 11) showing γ80 oscillations (top) and dyskinetic symptoms (bottom) following topical application of SCH23390 (red) or saline (blue), respectively (γ80 power expressed relative to the pink noise background). Note the parallel decline in the power of the resonant LFP oscillation and the dyskinesia score in all experiments (traces during the period of drug application are linearly interpolated). Right, Average data from all experiments showing significant differences between D1R-antagonist vs vehicle treatment before (darker colors) and after topical application. Error bars denote SEM. *p < 0.05. D, Characterization of the relationship between γ80 and severity of dyskinesia during the early dyskinetic phase (first 40 min following levodopa injection) and the cessation of dyskinesia following topical application of SCH23390. Each panel represents a single experiment (n = 5 rats) and displays the dyskinesia score as a function of cortical γ80 power (each symbol denotes average over a 1 min period: filled, early dyskinetic phase; open, cessation of dyskinesia following SCH23390). The relationships were well fitted with sigmoid functions (average goodness-of-fit, R2 = 0.72 ± 0.22). Notably, a similar relation between γ80 power and the severity of dyskinesia is evident during the early phase of dyskinesia and following pharmacological γ80 suppression.

    Techniques Used: Activation Assay, Immunohistochemical staining, Staining, Expressing, Injection

    Similar Products

  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86
    Millipore rabbit antibody against d1r
    Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on <t>D1R–GluN1</t> interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of <t>D1R–GluN1</t> interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
    Rabbit Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars
      Buy from Supplier

    86
    Millipore rabbit primary antibody against d1r
    Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on <t>D1R–GluN1</t> interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of <t>D1R–GluN1</t> interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
    Rabbit Primary Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit primary antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit primary antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars
      Buy from Supplier

    86
    Abcam rabbit antibody against d1r
    Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on <t>D1R–GluN1</t> interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of <t>D1R–GluN1</t> interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
    Rabbit Antibody Against D1r, supplied by Abcam, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit antibody against d1r/product/Abcam
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars
      Buy from Supplier

    86
    Millipore rabbit polyclonal antibodies against da receptors d1r
    Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on <t>D1R–GluN1</t> interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of <t>D1R–GluN1</t> interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
    Rabbit Polyclonal Antibodies Against Da Receptors D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibodies against da receptors d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal antibodies against da receptors d1r - by Bioz Stars, 2024-09
    86/100 stars
      Buy from Supplier

    86
    Millipore rabbit polyclonal antibody against d1r
    Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on <t>D1R–GluN1</t> interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of <t>D1R–GluN1</t> interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.
    Rabbit Polyclonal Antibody Against D1r, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibody against d1r/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal antibody against d1r - by Bioz Stars, 2024-09
    86/100 stars
      Buy from Supplier

    Image Search Results


    Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.

    Journal: Drug Design, Development and Therapy

    Article Title: Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats

    doi: 10.2147/DDDT.S93487

    Figure Lengend Snippet: Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.

    Article Snippet: Samples were incubated with a rabbit antibody against D1R (EMD Millipore, Billerica, MA, USA) or a mouse antibody against GluN1 (Millipore) overnight at 4°C.

    Techniques: Injection, Immunoprecipitation, Western Blot

    Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Journal: Drug Design, Development and Therapy

    Article Title: Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats

    doi: 10.2147/DDDT.S93487

    Figure Lengend Snippet: Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Article Snippet: Samples were incubated with a rabbit antibody against D1R (EMD Millipore, Billerica, MA, USA) or a mouse antibody against GluN1 (Millipore) overnight at 4°C.

    Techniques: Expressing, Western Blot

    Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.

    Journal: Drug Design, Development and Therapy

    Article Title: Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats

    doi: 10.2147/DDDT.S93487

    Figure Lengend Snippet: Effects of intrastriatal administration of Tat-fusion interfering peptide (Tat-D1Ri) on D1R–GluN1 interactions. Notes: Tat-D1Ri, Tat-D1Rc, or saline were locally injected into the striatum of the normal adult rat at a rate of 0.2 µL/min. Rat striatal tissues were then used for coimmunoprecipitation experiments to validate the efficacy and selectivity of interfering peptide. The intrastriatal injection of Tat-D1Ri rather than Tat-D1Rc caused reduction of D1R–GluN1 interactions, which demonstrated the effectiveness of Tat-D1Ri. Abbreviations: Tat-D1Rc, Tat-fusion control peptide; Ig, Immunoglobulin; IP, immunoprecipitation; IB, immunoblot.

    Article Snippet: Membranes were blocked in 5% nonfat milk for 1 hour at room temperature and incubated with a rabbit primary antibody against D1R (Millipore) or a mouse primary antibody against GluN1 (Millipore) overnight at 4°C.

    Techniques: Injection, Immunoprecipitation, Western Blot

    Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Journal: Drug Design, Development and Therapy

    Article Title: Targeting the D1-N-methyl- d -aspartate receptor complex reduces l -dopa-induced dyskinesia in 6-hydroxydopamine-lesioned Parkinson’s rats

    doi: 10.2147/DDDT.S93487

    Figure Lengend Snippet: Effects of intrastriatal administration of Tat-D1Ri on membrane D1R subunit expression. Notes: Protein levels were evaluated by Western blotting of proteins extracted from the lesioned striatum of the rat brains. They were assessed in extracts from 6-OHDA-lesioned rats treated with pulsatile l -dopa plus intrastriatal administration of Tat-D1Rc or Tat-D1Ri. ( A ) Representative Western blot analysis of D1R in the membrane fraction; ( B ) densitometric analysis of two blots with specific protein signals normalized to the corresponding GAPDH levels. Data are expressed as means ± SEM. Statistical analysis was conducted by independent-samples t -test. * P =0.05 versus LID + Tat-D1Rc. Abbreviations: 6-OHDA, 6-hydroxydopamine; l -dopa, L-3,4-dihydroxyphenylalanine; LID, l -dopa-induced dyskinesia; SEM, standard error of mean; Tat-D1Ri, Tat-fusion interfering peptide; Tat-D1Rc, Tat-fusion control peptide; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Article Snippet: Membranes were blocked in 5% nonfat milk for 1 hour at room temperature and incubated with a rabbit primary antibody against D1R (Millipore) or a mouse primary antibody against GluN1 (Millipore) overnight at 4°C.

    Techniques: Expressing, Western Blot