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Proteintech rabbit polyclonal anti cbs antibody
Reagents and instruments used in the study
Rabbit Polyclonal Anti Cbs Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "Hydrogen sulfide reduces oxidative stress in Huntington’s disease via Nrf2"

Article Title: Hydrogen sulfide reduces oxidative stress in Huntington’s disease via Nrf2

Journal: Neural Regeneration Research

doi: 10.4103/NRR.NRR-D-23-01051

Reagents and instruments used in the study
Figure Legend Snippet: Reagents and instruments used in the study

Techniques Used: CCK-8 Assay, Saline, TUNEL Assay, DNA Extraction, Modification, Marker, Fluorescence, Microscopy, Imaging



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Proteintech rabbit polyclonal anti cbs antibody
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ABclonal Biotechnology anti cb 2 r rabbit polyclonal abclonal cat a1762 1 1000 dilution
CB 1 R and <t>CB</t> <t>2</t> <t>R</t> expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.
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<t>CB</t> <t>1</t> <t>R</t> and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.
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<t>CB</t> <t>1</t> <t>R</t> and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.
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Proteintech rabbit polyclonal anti cbs
<t>CB</t> <t>1</t> <t>R</t> and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.
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Boster Bio primary rabbit anti cbs cbs polyclonal antibody
<t>CB</t> <t>1</t> <t>R</t> and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.
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Image Search Results


Reagents and instruments used in the study

Journal: Neural Regeneration Research

Article Title: Hydrogen sulfide reduces oxidative stress in Huntington’s disease via Nrf2

doi: 10.4103/NRR.NRR-D-23-01051

Figure Lengend Snippet: Reagents and instruments used in the study

Article Snippet: Rabbit polyclonal anti-CBS antibody , Proteintech Group , 14787-1-AP (RRID: AB_2070970).

Techniques: CCK-8 Assay, Saline, TUNEL Assay, DNA Extraction, Modification, Marker, Fluorescence, Microscopy, Imaging

CB 1 R and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.

Journal: PLOS ONE

Article Title: Cannabinoid receptor 1 positive allosteric modulator ZCZ011 shows differential effects on behavior and the endocannabinoid system in HIV-1 Tat transgenic female and male mice

doi: 10.1371/journal.pone.0305868

Figure Lengend Snippet: CB 1 R and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.

Article Snippet: Primary antibodies used in this study were, anti-CB 1 R (rabbit polyclonal; Proteintech, Cat# 17978-1-AP, 1:1000 dilution), anti-CB 2 R (rabbit polyclonal; AbClonal, Cat# A1762, 1:1000 dilution), anti-FAAH (mouse monoclonal; Abcam, Cat# ab54615, 1:1000 dilution), and anti-MAGL (rabbit polyclonal; Abcam, Cat# ab24701, 1:1000 dilution).

Techniques: Expressing, Western Blot

CB 1 R and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.

Journal: PLOS ONE

Article Title: Cannabinoid receptor 1 positive allosteric modulator ZCZ011 shows differential effects on behavior and the endocannabinoid system in HIV-1 Tat transgenic female and male mice

doi: 10.1371/journal.pone.0305868

Figure Lengend Snippet: CB 1 R and CB 2 R expression levels were assessed in the prefrontal cortex, striatum, and cerebellum for vehicle- and ZCZ011-treated Tat(–) and Tat(+) mice via Western blot analysis. Data were normalized to the housekeeping protein GAPDH. ( A ) Representative immunoblots for CB 1 R, CB 2 R, and GAPDH for all groups used in the study. ( B ) In the prefrontal cortex, no changes were observed in CB 1 R expression. In striatum and cerebellum, a main effect of sex was seen with females displaying higher levels of CB 1 R as compared to males. Additionally, ZCZ011 differentially affected CB 1 R expression based on genotype in the striatum and cerebellum. ( C ) In the prefrontal cortex and striatum, a main effect of sex was seen with males displaying higher level of CB 2 R in the prefrontal cortex and females displaying higher level of CB 2 R in the striatum. Further, Tat expression increased CB 2 R in the prefrontal cortex. In the cerebellum, no changes were observed in CB 2 R expression. All data are expressed as mean ± the standard error of the mean (SEM). Statistical significance was assessed by ANOVAs; λ p ≤ 0.05 main effect of sex; α p ≤ 0.005 main effect of genotype; φ p ≤ 0.05 main drug x genotype interaction; δ p ≤ 0.05 main genotype x sex interaction. Separate ANOVAs for females and males; ι p ≤ 0.05 genotype effect for females. Follow-up Tukey’s post hoc tests; * p ≤ 0.05. ZCZ011 dose = 10 mg/kg. N = 32(16f); AU, arbitrary unit.

Article Snippet: Primary antibodies used in this study were, anti-CB 1 R (rabbit polyclonal; Proteintech, Cat# 17978-1-AP, 1:1000 dilution), anti-CB 2 R (rabbit polyclonal; AbClonal, Cat# A1762, 1:1000 dilution), anti-FAAH (mouse monoclonal; Abcam, Cat# ab54615, 1:1000 dilution), and anti-MAGL (rabbit polyclonal; Abcam, Cat# ab24701, 1:1000 dilution).

Techniques: Expressing, Western Blot