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rabbit polyclonal anti pept1  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit polyclonal anti pept1
    Rabbit Polyclonal Anti Pept1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 84 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+pept1/pm30639584-63-10-15?v=Santa+Cruz+Biotechnology
    Average 94 stars, based on 84 article reviews
    rabbit polyclonal anti pept1 - by Bioz Stars, 2026-07
    94/100 stars

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    Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and <t>PepT1</t> (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).
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    Bioss pept1 rabbit bioss antibodies
    Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and <t>PepT1</t> (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).
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    Santa Cruz Biotechnology rabbit polyclonal anti pept1
    Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and <t>PepT1</t> (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).
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    Santa Cruz Biotechnology rabbit polyclonal pept1
    Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and <t>PepT1</t> (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).
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    Santa Cruz Biotechnology anti pept1 rabbit polyclonal antibody h 235
    Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and <t>PepT1</t> (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).
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    Santa Cruz Biotechnology pept 1 rabbit polyclonal antibodies
    Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and <t>PepT1</t> (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).
    Pept 1 Rabbit Polyclonal Antibodies, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Lampire Biological polyclonal rabbit anti-mouse pept1 antisera
    <t>PEPT1</t> mRNA expression in small intestinal and colonic segments of wild-type (+/+) mice during fed and fasted conditions. mRNA expression in the duodenum of fed mice was considered the control group and was arbitrarily assigned a value of unity. mRNA expression in other treatment groups was scaled to the control value. Data are reported as mean ± SE (n=6). Statistical differences between fed and fasted conditions for each tissue segment were determined using a two-sample student's t-test; *p ≤ 0.05.
    Polyclonal Rabbit Anti Mouse Pept1 Antisera, supplied by Lampire Biological, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and PepT1 (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).

    Journal: Animal Nutrition

    Article Title: Different copper sources and levels affect growth performance, copper content, carcass characteristics, intestinal microorganism and metabolism of finishing pigs

    doi: 10.1016/j.aninu.2021.10.007

    Figure Lengend Snippet: Effects of different copper sources and levels on the mRNA expression of CTR1 (A), ATP7A (B), ATOX1 (C), ASCT2 (D) and PepT1 (E) genes in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).

    Article Snippet: The membranes were blocked with 5% skim milk in Tris-buffered saline containing 0.05% Tween-20 (TBST) and incubated overnight at 4 °C with the antibodies: rabbit anti-CTR1 (1:1,000, Genetex, GTX30642), rabbit anti-PepT1 (1:1,000, Bioss, bs-0689R) and rabbit anti-actin (1:1,000, Absin, abs132001).

    Techniques: Expressing

    Effects of different copper sources and levels on the mRNA Expression of CTR1 (A), ATP7A (B), ATP7B (C), ATOX1 (D), ASCT2 (E) and PepT1 (F) genes in liver. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).

    Journal: Animal Nutrition

    Article Title: Different copper sources and levels affect growth performance, copper content, carcass characteristics, intestinal microorganism and metabolism of finishing pigs

    doi: 10.1016/j.aninu.2021.10.007

    Figure Lengend Snippet: Effects of different copper sources and levels on the mRNA Expression of CTR1 (A), ATP7A (B), ATP7B (C), ATOX1 (D), ASCT2 (E) and PepT1 (F) genes in liver. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; ATP7A = ATPase copper transporting alpha; ATOX1 = Antioxidant 1 copper chaperone; ASCT2 = lanine-serine-cysteine transporter, type-2; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).

    Article Snippet: The membranes were blocked with 5% skim milk in Tris-buffered saline containing 0.05% Tween-20 (TBST) and incubated overnight at 4 °C with the antibodies: rabbit anti-CTR1 (1:1,000, Genetex, GTX30642), rabbit anti-PepT1 (1:1,000, Bioss, bs-0689R) and rabbit anti-actin (1:1,000, Absin, abs132001).

    Techniques: Expressing

    Effects of different copper sources and levels on the protein expression for CTR1(A), and PepT1(B) in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).

    Journal: Animal Nutrition

    Article Title: Different copper sources and levels affect growth performance, copper content, carcass characteristics, intestinal microorganism and metabolism of finishing pigs

    doi: 10.1016/j.aninu.2021.10.007

    Figure Lengend Snippet: Effects of different copper sources and levels on the protein expression for CTR1(A), and PepT1(B) in jejunal mucosa. CuSO 4 = copper sulfate; Cu-Gly = copper glycinate; Cu-Pro = copper proteinate; CTR1 = high affinity copper uptake protein 1; PepT1 = peptide transporter 1. Data represent mean values ± standard error of the mean ( n = 6). Significant differences between processing treatments are represented by different lowercase letters ( P < 0.05).

    Article Snippet: The membranes were blocked with 5% skim milk in Tris-buffered saline containing 0.05% Tween-20 (TBST) and incubated overnight at 4 °C with the antibodies: rabbit anti-CTR1 (1:1,000, Genetex, GTX30642), rabbit anti-PepT1 (1:1,000, Bioss, bs-0689R) and rabbit anti-actin (1:1,000, Absin, abs132001).

    Techniques: Expressing

    PEPT1 mRNA expression in small intestinal and colonic segments of wild-type (+/+) mice during fed and fasted conditions. mRNA expression in the duodenum of fed mice was considered the control group and was arbitrarily assigned a value of unity. mRNA expression in other treatment groups was scaled to the control value. Data are reported as mean ± SE (n=6). Statistical differences between fed and fasted conditions for each tissue segment were determined using a two-sample student's t-test; *p ≤ 0.05.

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: PEPT1 mRNA expression in small intestinal and colonic segments of wild-type (+/+) mice during fed and fasted conditions. mRNA expression in the duodenum of fed mice was considered the control group and was arbitrarily assigned a value of unity. mRNA expression in other treatment groups was scaled to the control value. Data are reported as mean ± SE (n=6). Statistical differences between fed and fasted conditions for each tissue segment were determined using a two-sample student's t-test; *p ≤ 0.05.

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Expressing, Control

    PEPT1 protein expression in small intestinal and colonic segments of wild-type mice during fed and fasted conditions. For each tissue, protein expression in fed mice was considered the control group and was arbitrarily assigned a value of unity. Protein expression in fasted mice was scaled to the control value. Data are reported as mean ± SE (n=6). Statistical differences between fed and fasted conditions for each tissue segment were determined using a two-sample student's t-test; **p ≤ 0.01 and ***p ≤ 0.001. Relative protein expression levels in small intestinal and colonic segments have been reported previously (see reference 5, Fig 7).

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: PEPT1 protein expression in small intestinal and colonic segments of wild-type mice during fed and fasted conditions. For each tissue, protein expression in fed mice was considered the control group and was arbitrarily assigned a value of unity. Protein expression in fasted mice was scaled to the control value. Data are reported as mean ± SE (n=6). Statistical differences between fed and fasted conditions for each tissue segment were determined using a two-sample student's t-test; **p ≤ 0.01 and ***p ≤ 0.001. Relative protein expression levels in small intestinal and colonic segments have been reported previously (see reference 5, Fig 7).

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Expressing, Control

    Small intestinal transit, as determined at 30 min by a charcoal meal, during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice. Data are reported as mean ± SE (n=6). No statistical differences were observed using one-way ANOVA.

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Small intestinal transit, as determined at 30 min by a charcoal meal, during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice. Data are reported as mean ± SE (n=6). No statistical differences were observed using one-way ANOVA.

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Knock-Out

    Plasma concentration-time profiles of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice after 5 nmol/g intravenous bolus doses of dipeptide. Data are reported as mean ± SE (n=6).

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Plasma concentration-time profiles of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice after 5 nmol/g intravenous bolus doses of dipeptide. Data are reported as mean ± SE (n=6).

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Clinical Proteomics, Concentration Assay, Knock-Out

    Pharmacokinetics of [ 14 C]GlySar During Fed and Fasted Conditions in Wild-Type and  Pept1  Knockout Mice after 5 nmol/g Intravenous Bolus Doses of Dipeptide

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Pharmacokinetics of [ 14 C]GlySar During Fed and Fasted Conditions in Wild-Type and Pept1 Knockout Mice after 5 nmol/g Intravenous Bolus Doses of Dipeptide

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Drug discovery, Knock-Out

    Tissue distribution of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice, 120 min after 5 nmol/g intravenous bolus doses of dipeptide. Data are reported as mean ± SE (n=6). One-way ANOVA and Tukey method of multiple comparisons were performed to test for differences among treatment groups: ARepresents significant differences between fed and fasted conditions in wild-type mice; Brepresents significant differences between fed and fasted conditions in Pept1 knockout mice; Crepresents significant differences between wild-type and Pept1 knockout mice in fed conditions; and Drepresents significant differences between wild-type and Pept1 knockout mice in fasted conditions.

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Tissue distribution of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice, 120 min after 5 nmol/g intravenous bolus doses of dipeptide. Data are reported as mean ± SE (n=6). One-way ANOVA and Tukey method of multiple comparisons were performed to test for differences among treatment groups: ARepresents significant differences between fed and fasted conditions in wild-type mice; Brepresents significant differences between fed and fasted conditions in Pept1 knockout mice; Crepresents significant differences between wild-type and Pept1 knockout mice in fed conditions; and Drepresents significant differences between wild-type and Pept1 knockout mice in fasted conditions.

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Knock-Out

    Plasma concentration-time profiles of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice after 5 nmol/g oral doses of dipeptide. Data are reported as mean ± SE (n=6).

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Plasma concentration-time profiles of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice after 5 nmol/g oral doses of dipeptide. Data are reported as mean ± SE (n=6).

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Clinical Proteomics, Concentration Assay, Knock-Out

    Pharmacokinetics of [ 14 C]GlySar During Fed and Fasted Conditions in Wild-Type and  Pept1  Knockout Mice after 5 nmol/g Oral Doses of Dipeptide

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Pharmacokinetics of [ 14 C]GlySar During Fed and Fasted Conditions in Wild-Type and Pept1 Knockout Mice after 5 nmol/g Oral Doses of Dipeptide

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Drug discovery, Knock-Out

    Tissue distribution of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice, 360 min after 5 nmol/g oral doses of dipeptide. Data are reported as mean ± SE (n=6). No statistical differences were observed using one-way ANOVA.

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Tissue distribution of [14C]GlySar during fed and fasted conditions in wild-type (+/+) and Pept1 knockout (-/-) mice, 360 min after 5 nmol/g oral doses of dipeptide. Data are reported as mean ± SE (n=6). No statistical differences were observed using one-way ANOVA.

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Knock-Out

    Histology of the jejunum during fed conditions in wild-type (+/+) mice (a, b) and Pept1 knockout (-/-) mice (c, d). Sections were stained with hematoxylin and eosin, and examined by light microscopy. In (a) and (c), the bar = 1 mm; in (b) and (d), the bar = 100 μm.

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Histology of the jejunum during fed conditions in wild-type (+/+) mice (a, b) and Pept1 knockout (-/-) mice (c, d). Sections were stained with hematoxylin and eosin, and examined by light microscopy. In (a) and (c), the bar = 1 mm; in (b) and (d), the bar = 100 μm.

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Knock-Out, Staining, Light Microscopy

    Histology of the jejunum during fasted conditions in wild-type (+/+) mice (a, b) and Pept1 knockout (-/-) mice (c, d). Sections were stained with hematoxylin and eosin, and examined by light microscopy. In (a) and (c), the bar = 1 mm; in (b) and (d), the bar = 100 μm.

    Journal: Pharmaceutical Research

    Article Title: Influence of Fed-Fasted State on Intestinal PEPT1 Expression and In Vivo Pharmacokinetics of Glycylsarcosine in Wild-Type and Pept1 Knockout Mice

    doi: 10.1007/s11095-011-0580-9

    Figure Lengend Snippet: Histology of the jejunum during fasted conditions in wild-type (+/+) mice (a, b) and Pept1 knockout (-/-) mice (c, d). Sections were stained with hematoxylin and eosin, and examined by light microscopy. In (a) and (c), the bar = 1 mm; in (b) and (d), the bar = 100 μm.

    Article Snippet: Total protein from the mucus layers of mouse small intestine and colon was resolved on 7.5% SDS-PAGE, transferred to a PVDF membrane, and blotted with specific polyclonal rabbit anti-mouse PEPT1 antisera (raised against the COOH- terminal region, KGIGKENPYSSLEPVSQTNM; Lampire Biological Laboratories, Pipersville, PA) (1:1000 dilution) ( 5 , 17 ).

    Techniques: Knock-Out, Staining, Light Microscopy