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haptoglobin d type  (Randox)


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    Randox haptoglobin d type
    Haptoglobin D Type, supplied by Randox, used in various techniques. Bioz Stars score: 93/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/haptoglobin d type/product/Randox
    Average 93 stars, based on 27 article reviews
    haptoglobin d type - by Bioz Stars, 2026-02
    93/100 stars

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    Lack of IEC neutral ceramidase prevents DSS‐induced colitis. Asah2 ΔIEC and Asah2 fl/fl mice were treated with 2.5% DSS in drinking water for 12 days. A) Weight loss in animals following the induction of colitis, measured as a reduction from initial weight until the day of sacrifice. Data were analyzed by two‐way repeated‐measures ANOVA followed by Tukey's posttest. B) Colon images and length. C,D) Scores for rectal bleeding (C) and blood in stools (D). E) Representative histology staining and histological score of colons. F) Crypt depth of the distal colon. G–I) TUNEL (G) and Ki67 (H), and alcian blue (I) staining of the colon. J,K) Immunohistochemistry staining of occludin (J) and <t>haptoglobin</t> (K) proteins in the colon. L) Real‐time PCR analysis of indicated genes in the colon. Statistical comparisons were performed using a two‐tailed unpaired t ‐test, Error bars indicate mean ± SD. * p < 0.05, ** p < 0.01, *** p < 0.001. n = 8 (A). Each dot represents one mouse (B–D). Scale bar represents 50 µm.
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    Effect of induced vs. spontaneous parturition on plasma metabolites in neonatal and suckling piglets. Plasma metabolites exhibiting significant differences for specific time points comprised ( A ) ammonia, ( B ), creatinine, ( C ), glucose, ( D ) <t>haptoglobin,</t> ( E ) lactate, ( F ) NEFA (non-esterified fatty acids), ( G ) sodium, ( H ) total protein, ( I ) blood urea nitrogen, and ( J ) uric acid. Samples were taken at 0.5–6.0 h, day 1, day 4, day 20, and day 29. Data on induced parturitions also have been analysed in a companion study . Significant differences ( P < 0.05) are indicated by asterisks
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    Lack of IEC neutral ceramidase prevents DSS‐induced colitis. Asah2 ΔIEC and Asah2 fl/fl mice were treated with 2.5% DSS in drinking water for 12 days. A) Weight loss in animals following the induction of colitis, measured as a reduction from initial weight until the day of sacrifice. Data were analyzed by two‐way repeated‐measures ANOVA followed by Tukey's posttest. B) Colon images and length. C,D) Scores for rectal bleeding (C) and blood in stools (D). E) Representative histology staining and histological score of colons. F) Crypt depth of the distal colon. G–I) TUNEL (G) and Ki67 (H), and alcian blue (I) staining of the colon. J,K) Immunohistochemistry staining of occludin (J) and haptoglobin (K) proteins in the colon. L) Real‐time PCR analysis of indicated genes in the colon. Statistical comparisons were performed using a two‐tailed unpaired t ‐test, Error bars indicate mean ± SD. * p < 0.05, ** p < 0.01, *** p < 0.001. n = 8 (A). Each dot represents one mouse (B–D). Scale bar represents 50 µm.

    Journal: Advanced Science

    Article Title: Intestinal Neutral Ceramidase Deficiency Triggers Regulatory T Cell Response via Gd3 to Protect the Host from Intestinal Inflammation

    doi: 10.1002/advs.202512681

    Figure Lengend Snippet: Lack of IEC neutral ceramidase prevents DSS‐induced colitis. Asah2 ΔIEC and Asah2 fl/fl mice were treated with 2.5% DSS in drinking water for 12 days. A) Weight loss in animals following the induction of colitis, measured as a reduction from initial weight until the day of sacrifice. Data were analyzed by two‐way repeated‐measures ANOVA followed by Tukey's posttest. B) Colon images and length. C,D) Scores for rectal bleeding (C) and blood in stools (D). E) Representative histology staining and histological score of colons. F) Crypt depth of the distal colon. G–I) TUNEL (G) and Ki67 (H), and alcian blue (I) staining of the colon. J,K) Immunohistochemistry staining of occludin (J) and haptoglobin (K) proteins in the colon. L) Real‐time PCR analysis of indicated genes in the colon. Statistical comparisons were performed using a two‐tailed unpaired t ‐test, Error bars indicate mean ± SD. * p < 0.05, ** p < 0.01, *** p < 0.001. n = 8 (A). Each dot represents one mouse (B–D). Scale bar represents 50 µm.

    Article Snippet: For immunohistochemistry (IHC) studies, tissue sections were stained with the following antibodies: anti‐Occludin (BS‐1495R, Bioss), anti‐ haptoglobin (HP) (BS‐1808R, Bioss), and anti‐Ki‐67 (1:200, clone SolA15, Thermo Fisher Scientific).

    Techniques: Staining, TUNEL Assay, Immunohistochemistry, Real-time Polymerase Chain Reaction, Two Tailed Test

    Effect of induced vs. spontaneous parturition on plasma metabolites in neonatal and suckling piglets. Plasma metabolites exhibiting significant differences for specific time points comprised ( A ) ammonia, ( B ), creatinine, ( C ), glucose, ( D ) haptoglobin, ( E ) lactate, ( F ) NEFA (non-esterified fatty acids), ( G ) sodium, ( H ) total protein, ( I ) blood urea nitrogen, and ( J ) uric acid. Samples were taken at 0.5–6.0 h, day 1, day 4, day 20, and day 29. Data on induced parturitions also have been analysed in a companion study . Significant differences ( P < 0.05) are indicated by asterisks

    Journal: BMC Veterinary Research

    Article Title: Impact of parturition induction, farrowing environment and birth weight class on endocrine and metabolic plasma parameters related to piglet vitality

    doi: 10.1186/s12917-025-04845-2

    Figure Lengend Snippet: Effect of induced vs. spontaneous parturition on plasma metabolites in neonatal and suckling piglets. Plasma metabolites exhibiting significant differences for specific time points comprised ( A ) ammonia, ( B ), creatinine, ( C ), glucose, ( D ) haptoglobin, ( E ) lactate, ( F ) NEFA (non-esterified fatty acids), ( G ) sodium, ( H ) total protein, ( I ) blood urea nitrogen, and ( J ) uric acid. Samples were taken at 0.5–6.0 h, day 1, day 4, day 20, and day 29. Data on induced parturitions also have been analysed in a companion study . Significant differences ( P < 0.05) are indicated by asterisks

    Article Snippet: Plasma haptoglobin (cat.-no. HAPT-9, Life Diagnostics, Inc., West Chester, Pennsylvania, USA), cortisol (cat.-no. EIA-1887, DRG Diagnostics GmbH, Marburg, Germany), insulin (cat.-no. EIA-4747, DRG Diagnostics GmbH), and total triiodothyronine (cat.-no. EIA-4569, DRG Diagnostics GmbH) were measured in duplicate via ELISAs according to the manufacturer’s protocol.

    Techniques: Clinical Proteomics