glua2 n-terminus Search Results


glua2 (n-terminus) alomone agp-073  (Alomone Labs)
92
Alomone Labs glua2 (n-terminus) alomone agp-073
Glua2 (N Terminus) Alomone Agp 073, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/glua2 (n-terminus) alomone agp-073/product/Alomone Labs
Average 92 stars, based on 1 article reviews
glua2 (n-terminus) alomone agp-073 - by Bioz Stars, 2026-05
92/100 stars
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rabbit anti glur2  (Cell Signaling Technology Inc)
94
Cell Signaling Technology Inc rabbit anti glur2
Statistical results for measured mRNA
Rabbit Anti Glur2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit anti glur2/product/Cell Signaling Technology Inc
Average 94 stars, based on 1 article reviews
rabbit anti glur2 - by Bioz Stars, 2026-05
94/100 stars
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Image Search Results


Statistical results for measured mRNA

Journal: Neuroscience

Article Title: Connexin and AMPA Receptor Expression Changes Over Time in the Rat Olfactory Bulb

doi: 10.1016/j.neuroscience.2012.06.070

Figure Lengend Snippet: Statistical results for measured mRNA

Article Snippet: Primary antisera used in this study were purchased from Cell Signaling Technology (CST; Danvers, MA, USA), Invitrogen, Millipore (Billerica, MA, USA), and Sigma–Aldrich and are as follows, with the epitope, dilution/buffer, and catalog number in parentheses: Invitrogen rabbit anti-Cx36 (cytoplasmic loop between second and third transmembrane domains; 1:250 in 4% milk/TBST; 51-6200), Invitrogen rabbit anti-Cx36 (C-terminus; 1:250 in 1% milk/TBST; 51-6300), Invitrogen mouse anti-Cx36 (C-terminus; 1:500 in 4% milk/TBST; 37-4600), Invitrogen rabbit anti-Cx43 (C-terminus; 1:500 in OBBT; 71-0700), Invitrogen rabbit anti-Cx45 (C-terminus; 1:250/OBBT; 40-7000), Millipore mouse anti-GluR1 (N-terminus; 1:500/OBBT; MAB2263), CST rabbit anti-GluR2 (N-terminus; 1:500/OBBT; 5306S), CST rabbit anti-GluR3 (residues surrounding Pro590 of human GluR3; 1:1500/OBBT; 4676S), CST rabbit anti-GluR4 (residues surrounding Gln890 of human GluR4; 1:1000 in 5% bovine serum albumin/TBST*; 8070S), CST mouse anti-β-III-tubulin (C-terminus; 1:2000/OBBT; 4466S), and Sigma–Aldrich rabbit anti-β-III-tubulin (residues 442–446; 1:5000 in 4% milk/TBST; SAB4300623).

Techniques:

Changes in α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) subunit mRNA across dark and light phases in rat OB. Line plots of (A) GluR1, (B) GluR2, (C) GluR3, and (D) GluR4 mRNA expression over 48-h. Sample size and notation as in Fig. 1. GluR1, GluR2, and GluR3 mRNA changes were statistically significant across the 48-h (Kruskal–Wallis H test, P < 0.05) but only GluR1 was rhythmic for both 24-h periods (harmonic regression analysis, P < 0.05). GluR1 and GluR4 were rhythmic according to JTK_CYCLE analysis (P < 0.05).

Journal: Neuroscience

Article Title: Connexin and AMPA Receptor Expression Changes Over Time in the Rat Olfactory Bulb

doi: 10.1016/j.neuroscience.2012.06.070

Figure Lengend Snippet: Changes in α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) subunit mRNA across dark and light phases in rat OB. Line plots of (A) GluR1, (B) GluR2, (C) GluR3, and (D) GluR4 mRNA expression over 48-h. Sample size and notation as in Fig. 1. GluR1, GluR2, and GluR3 mRNA changes were statistically significant across the 48-h (Kruskal–Wallis H test, P < 0.05) but only GluR1 was rhythmic for both 24-h periods (harmonic regression analysis, P < 0.05). GluR1 and GluR4 were rhythmic according to JTK_CYCLE analysis (P < 0.05).

Article Snippet: Primary antisera used in this study were purchased from Cell Signaling Technology (CST; Danvers, MA, USA), Invitrogen, Millipore (Billerica, MA, USA), and Sigma–Aldrich and are as follows, with the epitope, dilution/buffer, and catalog number in parentheses: Invitrogen rabbit anti-Cx36 (cytoplasmic loop between second and third transmembrane domains; 1:250 in 4% milk/TBST; 51-6200), Invitrogen rabbit anti-Cx36 (C-terminus; 1:250 in 1% milk/TBST; 51-6300), Invitrogen mouse anti-Cx36 (C-terminus; 1:500 in 4% milk/TBST; 37-4600), Invitrogen rabbit anti-Cx43 (C-terminus; 1:500 in OBBT; 71-0700), Invitrogen rabbit anti-Cx45 (C-terminus; 1:250/OBBT; 40-7000), Millipore mouse anti-GluR1 (N-terminus; 1:500/OBBT; MAB2263), CST rabbit anti-GluR2 (N-terminus; 1:500/OBBT; 5306S), CST rabbit anti-GluR3 (residues surrounding Pro590 of human GluR3; 1:1500/OBBT; 4676S), CST rabbit anti-GluR4 (residues surrounding Gln890 of human GluR4; 1:1000 in 5% bovine serum albumin/TBST*; 8070S), CST mouse anti-β-III-tubulin (C-terminus; 1:2000/OBBT; 4466S), and Sigma–Aldrich rabbit anti-β-III-tubulin (residues 442–446; 1:5000 in 4% milk/TBST; SAB4300623).

Techniques: Expressing

Changes in AMPAR subunit protein expressed in the rat OB membrane across light and dark phases in rat OB. (A) Anti-GluR1 (1:500) and (B) anti-GluR2 (1:500) using experimental design, analysis, notation, sample size, and statistical metric as in Fig. 4. Nitrocellulose blots were stripped and reprobed with anti-β-III-tubulin (1:2000). Arrows indicate expected size in kilodaltons (Mr = 110 kDa for GluR1, 100 kDa for GluR2, and 50 kDa for tubulin). GluR1 and GluR2 protein changes were statistically significant across the 48 h (Kruskal–Wallis H test, P < 0.05) but only GluR2 protein expression was rhythmic in the 24-h tested (harmonic regression analysis, P < 0.05). GluR1 and GluR2 protein expression was statistically significant for JTK_CYCLE analysis (P < 0.05).

Journal: Neuroscience

Article Title: Connexin and AMPA Receptor Expression Changes Over Time in the Rat Olfactory Bulb

doi: 10.1016/j.neuroscience.2012.06.070

Figure Lengend Snippet: Changes in AMPAR subunit protein expressed in the rat OB membrane across light and dark phases in rat OB. (A) Anti-GluR1 (1:500) and (B) anti-GluR2 (1:500) using experimental design, analysis, notation, sample size, and statistical metric as in Fig. 4. Nitrocellulose blots were stripped and reprobed with anti-β-III-tubulin (1:2000). Arrows indicate expected size in kilodaltons (Mr = 110 kDa for GluR1, 100 kDa for GluR2, and 50 kDa for tubulin). GluR1 and GluR2 protein changes were statistically significant across the 48 h (Kruskal–Wallis H test, P < 0.05) but only GluR2 protein expression was rhythmic in the 24-h tested (harmonic regression analysis, P < 0.05). GluR1 and GluR2 protein expression was statistically significant for JTK_CYCLE analysis (P < 0.05).

Article Snippet: Primary antisera used in this study were purchased from Cell Signaling Technology (CST; Danvers, MA, USA), Invitrogen, Millipore (Billerica, MA, USA), and Sigma–Aldrich and are as follows, with the epitope, dilution/buffer, and catalog number in parentheses: Invitrogen rabbit anti-Cx36 (cytoplasmic loop between second and third transmembrane domains; 1:250 in 4% milk/TBST; 51-6200), Invitrogen rabbit anti-Cx36 (C-terminus; 1:250 in 1% milk/TBST; 51-6300), Invitrogen mouse anti-Cx36 (C-terminus; 1:500 in 4% milk/TBST; 37-4600), Invitrogen rabbit anti-Cx43 (C-terminus; 1:500 in OBBT; 71-0700), Invitrogen rabbit anti-Cx45 (C-terminus; 1:250/OBBT; 40-7000), Millipore mouse anti-GluR1 (N-terminus; 1:500/OBBT; MAB2263), CST rabbit anti-GluR2 (N-terminus; 1:500/OBBT; 5306S), CST rabbit anti-GluR3 (residues surrounding Pro590 of human GluR3; 1:1500/OBBT; 4676S), CST rabbit anti-GluR4 (residues surrounding Gln890 of human GluR4; 1:1000 in 5% bovine serum albumin/TBST*; 8070S), CST mouse anti-β-III-tubulin (C-terminus; 1:2000/OBBT; 4466S), and Sigma–Aldrich rabbit anti-β-III-tubulin (residues 442–446; 1:5000 in 4% milk/TBST; SAB4300623).

Techniques: Expressing

Statistical results for measured membrane/organelle protein

Journal: Neuroscience

Article Title: Connexin and AMPA Receptor Expression Changes Over Time in the Rat Olfactory Bulb

doi: 10.1016/j.neuroscience.2012.06.070

Figure Lengend Snippet: Statistical results for measured membrane/organelle protein

Article Snippet: Primary antisera used in this study were purchased from Cell Signaling Technology (CST; Danvers, MA, USA), Invitrogen, Millipore (Billerica, MA, USA), and Sigma–Aldrich and are as follows, with the epitope, dilution/buffer, and catalog number in parentheses: Invitrogen rabbit anti-Cx36 (cytoplasmic loop between second and third transmembrane domains; 1:250 in 4% milk/TBST; 51-6200), Invitrogen rabbit anti-Cx36 (C-terminus; 1:250 in 1% milk/TBST; 51-6300), Invitrogen mouse anti-Cx36 (C-terminus; 1:500 in 4% milk/TBST; 37-4600), Invitrogen rabbit anti-Cx43 (C-terminus; 1:500 in OBBT; 71-0700), Invitrogen rabbit anti-Cx45 (C-terminus; 1:250/OBBT; 40-7000), Millipore mouse anti-GluR1 (N-terminus; 1:500/OBBT; MAB2263), CST rabbit anti-GluR2 (N-terminus; 1:500/OBBT; 5306S), CST rabbit anti-GluR3 (residues surrounding Pro590 of human GluR3; 1:1500/OBBT; 4676S), CST rabbit anti-GluR4 (residues surrounding Gln890 of human GluR4; 1:1000 in 5% bovine serum albumin/TBST*; 8070S), CST mouse anti-β-III-tubulin (C-terminus; 1:2000/OBBT; 4466S), and Sigma–Aldrich rabbit anti-β-III-tubulin (residues 442–446; 1:5000 in 4% milk/TBST; SAB4300623).

Techniques: