anti pn peptide Search Results


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  • 85
    ProSci Incorporated anti app
    Improved cerebrovascular reactivity coincides with alterations in oxidative stress regulation. A, The responses of isolated arteries to ACh, CGRP, and NOS inhibition with l-NNA (10−5 m) of aged <t>APP</t> mice (▲) relative to wild-type (●) littermates (★p < 0.05, ★★p < 0.01, ★★★p < 0.001) were completely normalized in tempol-, NAC-, and pioglitazone (pio)-treated APP (△) mice, whereas they were unaffected in treated wild-type (○) mice (untreated vs treated APP mice, *p < 0.05, **p < 0.01, ***p < 0.001; n = 4–8 mice/group). B, Pioglitazone, but not NAC or tempol (data not shown), reversed <t>the</t> <t>SOD2</t> upregulation detected by Western blot in pial vessels of APP mice. Actin was used to normalize loading variation (n = 5–7 mice/group). C, All compounds attenuated the increased SOD2 immunoreactivity detected throughout the cortical neuropil of APP mice, but not the bulk of enzyme immunointensity in neuronal cell bodies (n = 3–5 mice/group). Scale bar, 20 μm. Error bars represent SEM.
    Anti App, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti app/product/ProSci Incorporated
    Average 85 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti app - by Bioz Stars, 2023-05
    85/100 stars
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    93
    Cell Signaling Technology Inc rabbit anti c peptide
    Improved cerebrovascular reactivity coincides with alterations in oxidative stress regulation. A, The responses of isolated arteries to ACh, CGRP, and NOS inhibition with l-NNA (10−5 m) of aged <t>APP</t> mice (▲) relative to wild-type (●) littermates (★p < 0.05, ★★p < 0.01, ★★★p < 0.001) were completely normalized in tempol-, NAC-, and pioglitazone (pio)-treated APP (△) mice, whereas they were unaffected in treated wild-type (○) mice (untreated vs treated APP mice, *p < 0.05, **p < 0.01, ***p < 0.001; n = 4–8 mice/group). B, Pioglitazone, but not NAC or tempol (data not shown), reversed <t>the</t> <t>SOD2</t> upregulation detected by Western blot in pial vessels of APP mice. Actin was used to normalize loading variation (n = 5–7 mice/group). C, All compounds attenuated the increased SOD2 immunoreactivity detected throughout the cortical neuropil of APP mice, but not the bulk of enzyme immunointensity in neuronal cell bodies (n = 3–5 mice/group). Scale bar, 20 μm. Error bars represent SEM.
    Rabbit Anti C Peptide, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti c peptide/product/Cell Signaling Technology Inc
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti c peptide - by Bioz Stars, 2023-05
    93/100 stars
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    93
    Alomone Labs anti mirp1 antibody
    Improved cerebrovascular reactivity coincides with alterations in oxidative stress regulation. A, The responses of isolated arteries to ACh, CGRP, and NOS inhibition with l-NNA (10−5 m) of aged <t>APP</t> mice (▲) relative to wild-type (●) littermates (★p < 0.05, ★★p < 0.01, ★★★p < 0.001) were completely normalized in tempol-, NAC-, and pioglitazone (pio)-treated APP (△) mice, whereas they were unaffected in treated wild-type (○) mice (untreated vs treated APP mice, *p < 0.05, **p < 0.01, ***p < 0.001; n = 4–8 mice/group). B, Pioglitazone, but not NAC or tempol (data not shown), reversed <t>the</t> <t>SOD2</t> upregulation detected by Western blot in pial vessels of APP mice. Actin was used to normalize loading variation (n = 5–7 mice/group). C, All compounds attenuated the increased SOD2 immunoreactivity detected throughout the cortical neuropil of APP mice, but not the bulk of enzyme immunointensity in neuronal cell bodies (n = 3–5 mice/group). Scale bar, 20 μm. Error bars represent SEM.
    Anti Mirp1 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti mirp1 antibody/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti mirp1 antibody - by Bioz Stars, 2023-05
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    93
    Alomone Labs rabbit anti fpr2
    Primary antibodies used in this study.
    Rabbit Anti Fpr2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti fpr2/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti fpr2 - by Bioz Stars, 2023-05
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    91
    TaKaRa mouse anti human col1a1
    Primary antibodies used in this study.
    Mouse Anti Human Col1a1, supplied by TaKaRa, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti human col1a1/product/TaKaRa
    Average 91 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mouse anti human col1a1 - by Bioz Stars, 2023-05
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    Image Search Results


    Improved cerebrovascular reactivity coincides with alterations in oxidative stress regulation. A, The responses of isolated arteries to ACh, CGRP, and NOS inhibition with l-NNA (10−5 m) of aged APP mice (▲) relative to wild-type (●) littermates (★p < 0.05, ★★p < 0.01, ★★★p < 0.001) were completely normalized in tempol-, NAC-, and pioglitazone (pio)-treated APP (△) mice, whereas they were unaffected in treated wild-type (○) mice (untreated vs treated APP mice, *p < 0.05, **p < 0.01, ***p < 0.001; n = 4–8 mice/group). B, Pioglitazone, but not NAC or tempol (data not shown), reversed the SOD2 upregulation detected by Western blot in pial vessels of APP mice. Actin was used to normalize loading variation (n = 5–7 mice/group). C, All compounds attenuated the increased SOD2 immunoreactivity detected throughout the cortical neuropil of APP mice, but not the bulk of enzyme immunointensity in neuronal cell bodies (n = 3–5 mice/group). Scale bar, 20 μm. Error bars represent SEM.

    Journal: The Journal of Neuroscience

    Article Title: Complete Rescue of Cerebrovascular Function in Aged Alzheimer's Disease Transgenic Mice by Antioxidants and Pioglitazone, a Peroxisome Proliferator-Activated Receptor γ Agonist

    doi: 10.1523/JNEUROSCI.3348-08.2008

    Figure Lengend Snippet: Improved cerebrovascular reactivity coincides with alterations in oxidative stress regulation. A, The responses of isolated arteries to ACh, CGRP, and NOS inhibition with l-NNA (10−5 m) of aged APP mice (▲) relative to wild-type (●) littermates (★p < 0.05, ★★p < 0.01, ★★★p < 0.001) were completely normalized in tempol-, NAC-, and pioglitazone (pio)-treated APP (△) mice, whereas they were unaffected in treated wild-type (○) mice (untreated vs treated APP mice, *p < 0.05, **p < 0.01, ***p < 0.001; n = 4–8 mice/group). B, Pioglitazone, but not NAC or tempol (data not shown), reversed the SOD2 upregulation detected by Western blot in pial vessels of APP mice. Actin was used to normalize loading variation (n = 5–7 mice/group). C, All compounds attenuated the increased SOD2 immunoreactivity detected throughout the cortical neuropil of APP mice, but not the bulk of enzyme immunointensity in neuronal cell bodies (n = 3–5 mice/group). Scale bar, 20 μm. Error bars represent SEM.

    Article Snippet: Membranes loaded with proteins (4–20 μg) were incubated with either rabbit anti-SOD1 [1:3000 (vessels)/1:10,000 (cortex); Stressgen], anti-SOD2 (1:20,000/1:10,000; Stressgen), anti-APP (1:2000/1:500; ProSci), anti-BACE1 (1:1000, Santa Cruz Biotechnology), mouse anti-endothelial NOS (eNOS; 1:500; BD Biosciences Transduction Laboratories), anti-cyclooxygenase-2 (COX-2; 1:200/1:100; Cayman), anti-p67 phox (1:200; BD Biosciences Transduction Laboratories), anti-Aβ (6E10, 1:1000/1:200; BioSource International), or anti-actin (1:10,000, Sigma), which was used to normalize loading variation.

    Techniques: Isolation, Inhibition, Western Blot

    Treatment effect on amyloidosis. A, APP mice had increased levels of APP in pial vessels (★★★p < 0.001) and cortex (data not shown), although levels of BACE1 were unchanged. They also displayed increased total soluble Aβ, as well as soluble and insoluble Aβ1–40 and Aβ1–42. Neither NAC (data not shown) nor pioglitazone (pio) had an effect on APP, its cleavage enzyme BACE1, or cleavage product Aβ. Actin was used to normalize loading variation (n = 5–7 mice/group). Sol, Soluble; white bars, wild type (WT); light gray bars, WT plus pio; black bars, APP; dark gray bars, APP plus pio. B, Aged APP mice featured extensive Aβ plaque deposition in the cortex and hippocampus (Hi), as evidenced by thioflavine S (left) and Aβ1–42 immunostaining (right), compared with wild-type littermates, which had no deposition (data not shown). The treatments did not affect Aβ plaque number or load (n = 5–6 mice/group). Scale bar, 300 μm. Error bars represent SEM.

    Journal: The Journal of Neuroscience

    Article Title: Complete Rescue of Cerebrovascular Function in Aged Alzheimer's Disease Transgenic Mice by Antioxidants and Pioglitazone, a Peroxisome Proliferator-Activated Receptor γ Agonist

    doi: 10.1523/JNEUROSCI.3348-08.2008

    Figure Lengend Snippet: Treatment effect on amyloidosis. A, APP mice had increased levels of APP in pial vessels (★★★p < 0.001) and cortex (data not shown), although levels of BACE1 were unchanged. They also displayed increased total soluble Aβ, as well as soluble and insoluble Aβ1–40 and Aβ1–42. Neither NAC (data not shown) nor pioglitazone (pio) had an effect on APP, its cleavage enzyme BACE1, or cleavage product Aβ. Actin was used to normalize loading variation (n = 5–7 mice/group). Sol, Soluble; white bars, wild type (WT); light gray bars, WT plus pio; black bars, APP; dark gray bars, APP plus pio. B, Aged APP mice featured extensive Aβ plaque deposition in the cortex and hippocampus (Hi), as evidenced by thioflavine S (left) and Aβ1–42 immunostaining (right), compared with wild-type littermates, which had no deposition (data not shown). The treatments did not affect Aβ plaque number or load (n = 5–6 mice/group). Scale bar, 300 μm. Error bars represent SEM.

    Article Snippet: Membranes loaded with proteins (4–20 μg) were incubated with either rabbit anti-SOD1 [1:3000 (vessels)/1:10,000 (cortex); Stressgen], anti-SOD2 (1:20,000/1:10,000; Stressgen), anti-APP (1:2000/1:500; ProSci), anti-BACE1 (1:1000, Santa Cruz Biotechnology), mouse anti-endothelial NOS (eNOS; 1:500; BD Biosciences Transduction Laboratories), anti-cyclooxygenase-2 (COX-2; 1:200/1:100; Cayman), anti-p67 phox (1:200; BD Biosciences Transduction Laboratories), anti-Aβ (6E10, 1:1000/1:200; BioSource International), or anti-actin (1:10,000, Sigma), which was used to normalize loading variation.

    Techniques: Immunostaining

    Primary antibodies used in this study.

    Journal: Annals of diagnostic pathology

    Article Title: Specialized pro-resolving receptors are expressed in salivary glands with Sjögren’s syndrome

    doi: 10.1016/j.anndiagpath.2021.151865

    Figure Lengend Snippet: Primary antibodies used in this study.

    Article Snippet: Also, rabbit Anti-FPR2 was obtained from Alomone Labs (Jerusalem, IL).

    Techniques:

    Distribution of SPM receptors within minor salivary glands from non-SS and SS patients. (A) ALX/FPR2 was expressed in mucous acini from both SS and non-SS patients (white arrows), while it was only observed within striated ducts from SS patients (yellow arrow). (B) BLT1 was found at the plasma membrane of both striated ducts (brown arrows) and mucous acini (pink arrows) of both SS and non-SS patients. (C) CMKLR1 was expressed in mucous acini (purple arrows) as well as striated ducts (orange arrows) of both SS and non-SS patients. Red and green arrows indicate inflammatory and endothelial cells, respectively. A representative image from n = 3 per experimental group is shown. Scale bars represent 50 μm.

    Journal: Annals of diagnostic pathology

    Article Title: Specialized pro-resolving receptors are expressed in salivary glands with Sjögren’s syndrome

    doi: 10.1016/j.anndiagpath.2021.151865

    Figure Lengend Snippet: Distribution of SPM receptors within minor salivary glands from non-SS and SS patients. (A) ALX/FPR2 was expressed in mucous acini from both SS and non-SS patients (white arrows), while it was only observed within striated ducts from SS patients (yellow arrow). (B) BLT1 was found at the plasma membrane of both striated ducts (brown arrows) and mucous acini (pink arrows) of both SS and non-SS patients. (C) CMKLR1 was expressed in mucous acini (purple arrows) as well as striated ducts (orange arrows) of both SS and non-SS patients. Red and green arrows indicate inflammatory and endothelial cells, respectively. A representative image from n = 3 per experimental group is shown. Scale bars represent 50 μm.

    Article Snippet: Also, rabbit Anti-FPR2 was obtained from Alomone Labs (Jerusalem, IL).

    Techniques: