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rabbit anti fabp6  (Biorbyt)


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    Structured Review

    Biorbyt rabbit anti fabp6
    Rabbit Anti Fabp6, supplied by Biorbyt, 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/product/rabbit+anti+fabp6/FABP6+antibody/pmc12599461-64-5-8
    Average 93 stars, based on 1 article reviews
    rabbit anti fabp6 - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    other:

    Article Title: Intestinal Dysbiosis Caused by Epithelial Fabp6 Gene Disruption Exacerbates Gut Inflammatory Disease
    Article Snippet: The primary Abs used were rabbit anti-FABP6 (orb412509; Biorbyt, Cambridge, UK) and mouse anti-GAPDH (sc-32233; Santa Cruz Biotechnology, Dallas, TX, USA).



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    ( A ) Representative immunohistochemistry images from pre-pouch and pouch biopsies for H&E, <t>FABP6,</t> CEACAM5, CA2 staining. ( B ) Histological enteritis score of pre-pouch and pouch samples. ( C ) Average gene expression in the bulk RNA-seq data from healthy pouch patients. ( D ) Average gene expression in the bulk RNA-seq data from patients with actively inflammatory pouches. The expressions in panel C and D are scaled in each column including prepouch and pouch. ( E ) The deconvolved cell type proportions in healthy pouches from bulk RNA-seq data. ( F ) The deconvolved cell type proportions in inflammatory pouches from bulk RNA-seq data.
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    Image Search Results


    ( A ) Representative immunohistochemistry images from pre-pouch and pouch biopsies for H&E, FABP6, CEACAM5, CA2 staining. ( B ) Histological enteritis score of pre-pouch and pouch samples. ( C ) Average gene expression in the bulk RNA-seq data from healthy pouch patients. ( D ) Average gene expression in the bulk RNA-seq data from patients with actively inflammatory pouches. The expressions in panel C and D are scaled in each column including prepouch and pouch. ( E ) The deconvolved cell type proportions in healthy pouches from bulk RNA-seq data. ( F ) The deconvolved cell type proportions in inflammatory pouches from bulk RNA-seq data.

    Journal: medRxiv

    Article Title: Multiomic analysis reveals cellular and epigenetic plasticity in intestinal pouches of ulcerative colitis patients

    doi: 10.1101/2023.11.11.23298309

    Figure Lengend Snippet: ( A ) Representative immunohistochemistry images from pre-pouch and pouch biopsies for H&E, FABP6, CEACAM5, CA2 staining. ( B ) Histological enteritis score of pre-pouch and pouch samples. ( C ) Average gene expression in the bulk RNA-seq data from healthy pouch patients. ( D ) Average gene expression in the bulk RNA-seq data from patients with actively inflammatory pouches. The expressions in panel C and D are scaled in each column including prepouch and pouch. ( E ) The deconvolved cell type proportions in healthy pouches from bulk RNA-seq data. ( F ) The deconvolved cell type proportions in inflammatory pouches from bulk RNA-seq data.

    Article Snippet: Primary antibodies used were rabbit anti-APOA4 (1:1,000, Sigma HPA001352), rabbit anti-FABP6 (1:200, Sigma HPA012601), mouse anti-CA2 (Santa Cruz Biotechnology sc-48351), and mouse anti-CEACAM5 (R&D Systems MAB41281).

    Techniques: Immunohistochemistry, Staining, Expressing, RNA Sequencing Assay

    Na–bile acid cotransport expression in human distal ileal villus cells. ASBT expression was significantly increased in villus cells from obese human ileum compared to normal BMI human ileum.

    Journal: Cells

    Article Title: Mechanism of Dyslipidemia in Obesity—Unique Regulation of Ileal Villus Cell Brush Border Membrane Sodium–Bile Acid Cotransport

    doi: 10.3390/cells8101197

    Figure Lengend Snippet: Na–bile acid cotransport expression in human distal ileal villus cells. ASBT expression was significantly increased in villus cells from obese human ileum compared to normal BMI human ileum.

    Article Snippet: The following antibodies were used to detect the expression of the specific proteins: Farnesoid X receptor: FXR, sc-25309, Santa Cruz Biotechnology, Inc., Dallas, TX, USA [ , ]; ileal bile-acid-binding protein: ILBABP, AP26370PU-N, OriGene Global, Rockville, MD, USA [ ]; organic solute transporter alpha: OSTα, SAB1306154, Sigma-Aldrich Corporation, St. Louis, MO, USA; and Ezrin: MA5-13862, Invitrogen Life Technologies, Carlsbad, CA, USA [ , ].

    Techniques: Expressing

    FXR and bile acid handling protein expression in Zucker rat villus cells. ( A ) FXR expression was significantly increased in ileal villus cells from OZR compared to LZR. ( B ). Ileal bile acid binding protein levels were also significantly increased in villus cells from OZR compared to leans. ( C ) Organic solute transporter alpha (OSTα) protein expression was significantly increased in villus cells from OZR compared to LZR. ( D ) OSTα protein expression was also increased in villus cell plasma membrane from OZR compared to LZR.

    Journal: Cells

    Article Title: Mechanism of Dyslipidemia in Obesity—Unique Regulation of Ileal Villus Cell Brush Border Membrane Sodium–Bile Acid Cotransport

    doi: 10.3390/cells8101197

    Figure Lengend Snippet: FXR and bile acid handling protein expression in Zucker rat villus cells. ( A ) FXR expression was significantly increased in ileal villus cells from OZR compared to LZR. ( B ). Ileal bile acid binding protein levels were also significantly increased in villus cells from OZR compared to leans. ( C ) Organic solute transporter alpha (OSTα) protein expression was significantly increased in villus cells from OZR compared to LZR. ( D ) OSTα protein expression was also increased in villus cell plasma membrane from OZR compared to LZR.

    Article Snippet: The following antibodies were used to detect the expression of the specific proteins: Farnesoid X receptor: FXR, sc-25309, Santa Cruz Biotechnology, Inc., Dallas, TX, USA [ , ]; ileal bile-acid-binding protein: ILBABP, AP26370PU-N, OriGene Global, Rockville, MD, USA [ ]; organic solute transporter alpha: OSTα, SAB1306154, Sigma-Aldrich Corporation, St. Louis, MO, USA; and Ezrin: MA5-13862, Invitrogen Life Technologies, Carlsbad, CA, USA [ , ].

    Techniques: Expressing, Binding Assay, Clinical Proteomics, Membrane