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rabbit anti tjp1 polyclonal antibodies  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti tjp1 polyclonal antibodies
    Rabbit Anti Tjp1 Polyclonal Antibodies, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 415 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+tjp1+polyclonal+antibodies/ZO-1+Rabbit+mAb/pm31566218-83-79-85
    Average 97 stars, based on 415 article reviews
    rabbit anti tjp1 polyclonal antibodies - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Protective effects of astaxanthin on lipopolysaccharide-induced inflammation in bovine endometrial epithelial cells†.
    Article Snippet: Astaxanthin (AST), a natural antioxidant carotenoid, has been shown to exert anti-inflammatory effects.. However, to our knowledge, no study has specifically addressed the potential protective effects of AST against bovine endometritis.. The purpose of this study was to examine whether treatment with AST could protect endometrial epithelial cells against lipopolysaccharide (LPS)-induced inflammatory injury.

    Incubation:

    Article Title: Protective effects of astaxanthin on lipopolysaccharide-induced inflammation in bovine endometrial epithelial cells†.
    Article Snippet: Astaxanthin (AST), a natural antioxidant carotenoid, has been shown to exert anti-inflammatory effects.. However, to our knowledge, no study has specifically addressed the potential protective effects of AST against bovine endometritis.. The purpose of this study was to examine whether treatment with AST could protect endometrial epithelial cells against lipopolysaccharide (LPS)-induced inflammatory injury.

    Bioprocessing:

    Article Title: Protective effects of astaxanthin on lipopolysaccharide-induced inflammation in bovine endometrial epithelial cells†.
    Article Snippet: Astaxanthin (AST), a natural antioxidant carotenoid, has been shown to exert anti-inflammatory effects.. However, to our knowledge, no study has specifically addressed the potential protective effects of AST against bovine endometritis.. The purpose of this study was to examine whether treatment with AST could protect endometrial epithelial cells against lipopolysaccharide (LPS)-induced inflammatory injury.



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    Image Search Results


    Effect of dietary 25-hydroxycholecalciferol supplementation on 18-day-old broiler chicken ileal protein abundance. In total, 24 birds were sampled on each sampling day (n = 12 birds of each treatment). Dietary treatments: VITD 3 = 5,000 IU of vitamin D 3 per kg of broiler chicken feed; 25 OHD 3 = 2,760 IU of 25-hydroxycholecalciferol + 2,240 of vitamin D 3 per kg of broiler chicken feed. Protein expression was measured using quantitative, fluorescent Western Blot relative to total protein. (A) IL-10, IL-17, ZO-1, and Claudin-1 protein abundance. (B) Day 18 representative fluorescent Western Blot. Abundance of IL-17 was grater for VITD3-fed birds. a,b Bars with different superscripts differ at P ≤ 0.05.

    Journal: Frontiers in Veterinary Science

    Article Title: Dietary 25-Hydroxyvitamin D3 Supplementation Modulates Intestinal Cytokines in Young Broiler Chickens

    doi: 10.3389/fvets.2022.947276

    Figure Lengend Snippet: Effect of dietary 25-hydroxycholecalciferol supplementation on 18-day-old broiler chicken ileal protein abundance. In total, 24 birds were sampled on each sampling day (n = 12 birds of each treatment). Dietary treatments: VITD 3 = 5,000 IU of vitamin D 3 per kg of broiler chicken feed; 25 OHD 3 = 2,760 IU of 25-hydroxycholecalciferol + 2,240 of vitamin D 3 per kg of broiler chicken feed. Protein expression was measured using quantitative, fluorescent Western Blot relative to total protein. (A) IL-10, IL-17, ZO-1, and Claudin-1 protein abundance. (B) Day 18 representative fluorescent Western Blot. Abundance of IL-17 was grater for VITD3-fed birds. a,b Bars with different superscripts differ at P ≤ 0.05.

    Article Snippet: Primary antibodies used were as follows: mouse monoclonal IgG2b anti-IL-10 (1:1,000 dilution; Cat. No. SC-365858; Santa Cruz Biotechnology; Santa Cruz, CA, USA); rabbit polyclonal IgG anti-Chicken IL-17 (1:2,000 dilution; Cat. No. LS C294849; Lifespan Biosciences; Seattle, WA, USA); mouse monoclonal IgG2b anti-claudin-1 (1:300 dilution; Cat. No. SC-166338; Santa Cruz Biotechnology; Santa Cruz, CA, USA); and rabbit polyclonal IgG anti-Rat TJP1/ZO-1 (1:1,500 dilution; Cat. No. LS C145545; Lifespan Biosciences; Seattle, WA, USA).

    Techniques: Sampling, Expressing, Western Blot

    Effect of dietary 25-hydroxycholecalciferol supplementation on 21-day-old broiler chicken ileal protein abundance. In total, twenty-four birds were sampled on each sampling day (n = 12 birds of each treatment). Dietary treatments: VITD 3 = 5,000 IU of vitamin D 3 per kg of broiler chicken feed; 25 OHD 3 = 2,760 IU of 25-hydroxycholecalciferol + 2,240 of vitamin D 3 per kg of broiler chicken feed. Protein expression was measured using quantitative, fluorescent Western Blot relative to total protein. (A) IL-10, IL-17, ZO-1, and Claudin-1 protein abundance. (B) Day 21 representative fluorescent Western Blot. Abundance of IL-10 and IL-17 was grater for VITD3-fed birds. a,b Bars with different superscripts differ at P ≤ 0.05.

    Journal: Frontiers in Veterinary Science

    Article Title: Dietary 25-Hydroxyvitamin D3 Supplementation Modulates Intestinal Cytokines in Young Broiler Chickens

    doi: 10.3389/fvets.2022.947276

    Figure Lengend Snippet: Effect of dietary 25-hydroxycholecalciferol supplementation on 21-day-old broiler chicken ileal protein abundance. In total, twenty-four birds were sampled on each sampling day (n = 12 birds of each treatment). Dietary treatments: VITD 3 = 5,000 IU of vitamin D 3 per kg of broiler chicken feed; 25 OHD 3 = 2,760 IU of 25-hydroxycholecalciferol + 2,240 of vitamin D 3 per kg of broiler chicken feed. Protein expression was measured using quantitative, fluorescent Western Blot relative to total protein. (A) IL-10, IL-17, ZO-1, and Claudin-1 protein abundance. (B) Day 21 representative fluorescent Western Blot. Abundance of IL-10 and IL-17 was grater for VITD3-fed birds. a,b Bars with different superscripts differ at P ≤ 0.05.

    Article Snippet: Primary antibodies used were as follows: mouse monoclonal IgG2b anti-IL-10 (1:1,000 dilution; Cat. No. SC-365858; Santa Cruz Biotechnology; Santa Cruz, CA, USA); rabbit polyclonal IgG anti-Chicken IL-17 (1:2,000 dilution; Cat. No. LS C294849; Lifespan Biosciences; Seattle, WA, USA); mouse monoclonal IgG2b anti-claudin-1 (1:300 dilution; Cat. No. SC-166338; Santa Cruz Biotechnology; Santa Cruz, CA, USA); and rabbit polyclonal IgG anti-Rat TJP1/ZO-1 (1:1,500 dilution; Cat. No. LS C145545; Lifespan Biosciences; Seattle, WA, USA).

    Techniques: Sampling, Expressing, Western Blot

    Effect of bird age on intestinal tight junction protein abundance. On each sampling day, a total of 24 birds (n = 12 birds per treatment) were selected for tissue collection. Protein expression was measured using quantitative, fluorescent Western Blot relative to total protein. (A) Duodenal ZO-1 abundance, (B) Duodenal Claudin-1 abundance, (C) Ileal ZO-1 abundance, and (D) Ileal Claudin-1 abundance. a− e Bars with different superscripts differ at P ≤ 0.05.

    Journal: Frontiers in Veterinary Science

    Article Title: Dietary 25-Hydroxyvitamin D3 Supplementation Modulates Intestinal Cytokines in Young Broiler Chickens

    doi: 10.3389/fvets.2022.947276

    Figure Lengend Snippet: Effect of bird age on intestinal tight junction protein abundance. On each sampling day, a total of 24 birds (n = 12 birds per treatment) were selected for tissue collection. Protein expression was measured using quantitative, fluorescent Western Blot relative to total protein. (A) Duodenal ZO-1 abundance, (B) Duodenal Claudin-1 abundance, (C) Ileal ZO-1 abundance, and (D) Ileal Claudin-1 abundance. a− e Bars with different superscripts differ at P ≤ 0.05.

    Article Snippet: Primary antibodies used were as follows: mouse monoclonal IgG2b anti-IL-10 (1:1,000 dilution; Cat. No. SC-365858; Santa Cruz Biotechnology; Santa Cruz, CA, USA); rabbit polyclonal IgG anti-Chicken IL-17 (1:2,000 dilution; Cat. No. LS C294849; Lifespan Biosciences; Seattle, WA, USA); mouse monoclonal IgG2b anti-claudin-1 (1:300 dilution; Cat. No. SC-166338; Santa Cruz Biotechnology; Santa Cruz, CA, USA); and rabbit polyclonal IgG anti-Rat TJP1/ZO-1 (1:1,500 dilution; Cat. No. LS C145545; Lifespan Biosciences; Seattle, WA, USA).

    Techniques: Sampling, Expressing, Western Blot