cb 2 shrna Search Results


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Santa Cruz Biotechnology cb 2 shrna
(A) Enhanced immunoprecipitation of the ERK1/2 (Lane 4) compared to vehicle-treated controls (Lane 3). Negative controls (Lanes 5 and 6) received the same concentration of β-Arrestin 2 antibody except that the coupling resin was replaced with control agarose resin that is not amine reactive. All columns were incubated with prefrontal cortex lysate (300 μg) from vehicle (Lanes 3 and 5 ) or CP55940 (Lanes 4 and 6) treated rats. Prefrontal cortex lysate (30 μg of protein) was used as an input control (Lane 1 and 2). (B) Increased pERK protein levels in CP55940 treated rats compared to vehicle treated rats. **p<0.01, significant effect of CP55940 treatment compared to vehicle-treated controls. (C) Increased membrane associated β-Arrestin 2 protein levels in PFCx of CP55940 treated rats. **p<0.01 significant effect of CP55940 treatment compared to vehicle-treated controls. (D) CP55940 treatment does not affect total ERK1/2 expression in the PFCx. (E) Increased β-Arrestin 2 mRNA levels in PFCx of CP55940 treated rats. *p<0.01 significant effect of CP55940 treatment compared to vehicle treated controls. (F) β-Arr2 <t>shRNA</t> lentivurs transfection prevents GP1a-induced increases in 5-HT2A receptor mRNA. **p<0.01, significant effect of GP1a treatment on 5-HT receptor mRNA levels in control shRNA tranfected cells compared 2A to vehicle-treated controls. ##p<0.01, significant effect of β-Arr2 shRNA transfection on the GP1a-induced upregulation of 5-HT2A receptors. Representative Western blots are shown in this figure and IOD was calculated as described in Experimental Procedures. The data represent mean ± SEM (n=6–8).
Cb 2 Shrna, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cb 2 shrna - by Bioz Stars, 2026-08
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Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of CB2 gene silencing results, individual duplex components or plasmids are also available upon request. Suitable
  Buy from Supplier

N/A
Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of CB2 gene silencing results, individual duplex components or plasmids are also available upon request.
  Buy from Supplier

N/A
Gene Silencers generally consist of pools of three to five target-specific 19-25 nucleotide sequences in length. For independent verification of CB2 gene silencing results, individual duplex components or plasmids are also available upon request.
  Buy from Supplier

Image Search Results


(A) Enhanced immunoprecipitation of the ERK1/2 (Lane 4) compared to vehicle-treated controls (Lane 3). Negative controls (Lanes 5 and 6) received the same concentration of β-Arrestin 2 antibody except that the coupling resin was replaced with control agarose resin that is not amine reactive. All columns were incubated with prefrontal cortex lysate (300 μg) from vehicle (Lanes 3 and 5 ) or CP55940 (Lanes 4 and 6) treated rats. Prefrontal cortex lysate (30 μg of protein) was used as an input control (Lane 1 and 2). (B) Increased pERK protein levels in CP55940 treated rats compared to vehicle treated rats. **p<0.01, significant effect of CP55940 treatment compared to vehicle-treated controls. (C) Increased membrane associated β-Arrestin 2 protein levels in PFCx of CP55940 treated rats. **p<0.01 significant effect of CP55940 treatment compared to vehicle-treated controls. (D) CP55940 treatment does not affect total ERK1/2 expression in the PFCx. (E) Increased β-Arrestin 2 mRNA levels in PFCx of CP55940 treated rats. *p<0.01 significant effect of CP55940 treatment compared to vehicle treated controls. (F) β-Arr2 shRNA lentivurs transfection prevents GP1a-induced increases in 5-HT2A receptor mRNA. **p<0.01, significant effect of GP1a treatment on 5-HT receptor mRNA levels in control shRNA tranfected cells compared 2A to vehicle-treated controls. ##p<0.01, significant effect of β-Arr2 shRNA transfection on the GP1a-induced upregulation of 5-HT2A receptors. Representative Western blots are shown in this figure and IOD was calculated as described in Experimental Procedures. The data represent mean ± SEM (n=6–8).

Journal: Pharmacological research : the official journal of the Italian Pharmacological Society

Article Title: Cannabinoid Agonists Increase the Interaction between ?-Arrestin 2 and ERK1/2 and Upregulate ?-Arrestin 2 and 5-HT 2A Receptors

doi: 10.1016/j.phrs.2012.11.002

Figure Lengend Snippet: (A) Enhanced immunoprecipitation of the ERK1/2 (Lane 4) compared to vehicle-treated controls (Lane 3). Negative controls (Lanes 5 and 6) received the same concentration of β-Arrestin 2 antibody except that the coupling resin was replaced with control agarose resin that is not amine reactive. All columns were incubated with prefrontal cortex lysate (300 μg) from vehicle (Lanes 3 and 5 ) or CP55940 (Lanes 4 and 6) treated rats. Prefrontal cortex lysate (30 μg of protein) was used as an input control (Lane 1 and 2). (B) Increased pERK protein levels in CP55940 treated rats compared to vehicle treated rats. **p<0.01, significant effect of CP55940 treatment compared to vehicle-treated controls. (C) Increased membrane associated β-Arrestin 2 protein levels in PFCx of CP55940 treated rats. **p<0.01 significant effect of CP55940 treatment compared to vehicle-treated controls. (D) CP55940 treatment does not affect total ERK1/2 expression in the PFCx. (E) Increased β-Arrestin 2 mRNA levels in PFCx of CP55940 treated rats. *p<0.01 significant effect of CP55940 treatment compared to vehicle treated controls. (F) β-Arr2 shRNA lentivurs transfection prevents GP1a-induced increases in 5-HT2A receptor mRNA. **p<0.01, significant effect of GP1a treatment on 5-HT receptor mRNA levels in control shRNA tranfected cells compared 2A to vehicle-treated controls. ##p<0.01, significant effect of β-Arr2 shRNA transfection on the GP1a-induced upregulation of 5-HT2A receptors. Representative Western blots are shown in this figure and IOD was calculated as described in Experimental Procedures. The data represent mean ± SEM (n=6–8).

Article Snippet: β-Arrestin 2 shRNA (r), CB 2 shRNA (r), CB 1 shRNA (r), copGFP control, control shRNA lentiviral particles, polybrene, and puromyocin were purchased from Santa Cruz, CA.

Techniques: Immunoprecipitation, Concentration Assay, Control, Incubation, Membrane, Expressing, shRNA, Transfection, Western Blot

(A) Reduced CB2 or CB1 mRNA levels in cells treated with CB2 or CB1 shRNA lentiviral particles, respectively. **p<0.01 significant effect of CB2 or CB1 shRNA compared to control shRNA treated cells. (B) CB2 shRNA lentivitrarus transfection prevents CP55940, JWH-133 and GP1a-induced increases in β-Arrestin 2 mRNA. **p<0.01, significant effect of CP55940, JWH-133, and GP1a treatment on β-Arrestin 2 mRNA levels in control shRNA lentivirus tranfected cells compared to vehicle-treated controls. ##p<0.01, significant effect of CB2 shRNA lentivirus transfection on the CP55940, JWH-133, and GP1a-induced upregulation of β-Arrestin 2. (C) CB1 shRNA lentivirus transfection does not prevent CP55940, JWH-133 or GP1a-induced increases β-Arrestin 2. **p<0.01, significant effect of CP55940, JWH-133 or GP1a treatment on β-Arrestin 2 mRNA levels in control or CB1 shRNA lentvirus treated cells compared to vehicle-treated controls. The data represent mean ± SEM (n=3).

Journal: Pharmacological research : the official journal of the Italian Pharmacological Society

Article Title: Cannabinoid Agonists Increase the Interaction between ?-Arrestin 2 and ERK1/2 and Upregulate ?-Arrestin 2 and 5-HT 2A Receptors

doi: 10.1016/j.phrs.2012.11.002

Figure Lengend Snippet: (A) Reduced CB2 or CB1 mRNA levels in cells treated with CB2 or CB1 shRNA lentiviral particles, respectively. **p<0.01 significant effect of CB2 or CB1 shRNA compared to control shRNA treated cells. (B) CB2 shRNA lentivitrarus transfection prevents CP55940, JWH-133 and GP1a-induced increases in β-Arrestin 2 mRNA. **p<0.01, significant effect of CP55940, JWH-133, and GP1a treatment on β-Arrestin 2 mRNA levels in control shRNA lentivirus tranfected cells compared to vehicle-treated controls. ##p<0.01, significant effect of CB2 shRNA lentivirus transfection on the CP55940, JWH-133, and GP1a-induced upregulation of β-Arrestin 2. (C) CB1 shRNA lentivirus transfection does not prevent CP55940, JWH-133 or GP1a-induced increases β-Arrestin 2. **p<0.01, significant effect of CP55940, JWH-133 or GP1a treatment on β-Arrestin 2 mRNA levels in control or CB1 shRNA lentvirus treated cells compared to vehicle-treated controls. The data represent mean ± SEM (n=3).

Article Snippet: β-Arrestin 2 shRNA (r), CB 2 shRNA (r), CB 1 shRNA (r), copGFP control, control shRNA lentiviral particles, polybrene, and puromyocin were purchased from Santa Cruz, CA.

Techniques: shRNA, Control, Transfection

(A) PD198306, potent ERK1/2 inhibitor, pretreatment prevents GP1a-induced increases β-Arrestin 2 mRNA levels. **p<0.01, significant effect of GP1a treatment compared to vehicle-treated controls. ##p<0.01, significant effect of PD198306 pretreatment on GP1a-induced increases β-Arrestin 2 mRNA levels compared to vehicle-treated controls (B) β-Arrestin 2 shRNA lentivirus treatment significantly reduced CP55940 induced increased in nuclear-associated pERK levels. **p<0.01, significant effect of CP55940 treatment on nuclear-associated pERK levels in control or β-Arrestin 2 shRNA treated cells compared to vehicle-treated. ##p<0.01, significant effect of β-Arrestin 2 shRNA treatment in CP55940 treated cells compared to control shRNA transfect/CP55940 treated cells. (C) β-Arrestin shRNA lentivirus treatment significantly reduced GP1a-induced increases in nuclear-associated pERK levels. **p<0.01, significant effect of GP1a treatment on nuclear-associated pERK levels in control or β-Arrestin 2 shRNA treated cells compared to vehicle-treated controls. ##p<0.01, significant effect of β-Arrestin 2 shRNA treatment in CP55940 treated cells compared to control shRNA transfected/CP55940 treated cells. The data represent mean ± SEM (n=3).

Journal: Pharmacological research : the official journal of the Italian Pharmacological Society

Article Title: Cannabinoid Agonists Increase the Interaction between ?-Arrestin 2 and ERK1/2 and Upregulate ?-Arrestin 2 and 5-HT 2A Receptors

doi: 10.1016/j.phrs.2012.11.002

Figure Lengend Snippet: (A) PD198306, potent ERK1/2 inhibitor, pretreatment prevents GP1a-induced increases β-Arrestin 2 mRNA levels. **p<0.01, significant effect of GP1a treatment compared to vehicle-treated controls. ##p<0.01, significant effect of PD198306 pretreatment on GP1a-induced increases β-Arrestin 2 mRNA levels compared to vehicle-treated controls (B) β-Arrestin 2 shRNA lentivirus treatment significantly reduced CP55940 induced increased in nuclear-associated pERK levels. **p<0.01, significant effect of CP55940 treatment on nuclear-associated pERK levels in control or β-Arrestin 2 shRNA treated cells compared to vehicle-treated. ##p<0.01, significant effect of β-Arrestin 2 shRNA treatment in CP55940 treated cells compared to control shRNA transfect/CP55940 treated cells. (C) β-Arrestin shRNA lentivirus treatment significantly reduced GP1a-induced increases in nuclear-associated pERK levels. **p<0.01, significant effect of GP1a treatment on nuclear-associated pERK levels in control or β-Arrestin 2 shRNA treated cells compared to vehicle-treated controls. ##p<0.01, significant effect of β-Arrestin 2 shRNA treatment in CP55940 treated cells compared to control shRNA transfected/CP55940 treated cells. The data represent mean ± SEM (n=3).

Article Snippet: β-Arrestin 2 shRNA (r), CB 2 shRNA (r), CB 1 shRNA (r), copGFP control, control shRNA lentiviral particles, polybrene, and puromyocin were purchased from Santa Cruz, CA.

Techniques: shRNA, Control, Transfection