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bile salt export protein  (Boster Bio)


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    Structured Review

    Boster Bio bile salt export protein
    Bile Salt Export Protein, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bile+salt+export+protein/Anti-ABCB11+Antibody+Picoband/pm40679478-115-56-70
    Average 94 stars, based on 13 article reviews
    bile salt export protein - by Bioz Stars, 2026-10
    94/100 stars

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    other:

    Article Title: Female ethanolamine phosphate phospholyase knockout mice resisted high-fat diet-induced obesity with attenuated hepatic cholesterol deposition.
    Article Snippet: Ethanolamine phosphate phospholyase (ETNPPL) is an enzyme that irreversibly degrades phosphoethanolamine (p-ETN), an intermediate in the Kennedy pathway of phosphatidylethanolamine (PE) synthesis.. Whole body knockout Etnppl mice were fed a high-fat diet (HFD) containing 45% kcal fat for 10 wk.. Etnppl / female mice were resistant to HFD-induced obesity and had decreased liver weight compared with Etnpplþ /þ mice.



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    Santa Cruz Biotechnology goat polyclonal anti-mouse bsep (bile salt export pump protein)
    Effect of L-FABP gene ablation on liver levels of key proteins involved in uptake, synthesis and storage of bile acid precursor cholesterol Liver homogenates of male mice were separated by SDS/PAGE and electroblotted on to nitrocellulose membranes as described in the Experimental section. The membranes were incubated with <t> polyclonal </t> antisera directed against proteins involved in cholesterol uptake (LDL receptor), efflux (SRB-1), synthesis (HMG-CoA reductase) and storage as cholesteryl esters (ACBP, ACAT-2 and ACAT-1). The amount of protein is expressed in arbitrary units (a.u.) with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): *, P <0.05; **, P <0.01. For cholesterol diet versus control diet: #, P <0.05; ###, P <0.001.
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    Effect of L-FABP gene ablation on liver levels of key proteins involved in uptake, synthesis and storage of bile acid precursor cholesterol Liver homogenates of male mice were separated by SDS/PAGE and electroblotted on to nitrocellulose membranes as described in the Experimental section. The membranes were incubated with  polyclonal  antisera directed against proteins involved in cholesterol uptake (LDL receptor), efflux (SRB-1), synthesis (HMG-CoA reductase) and storage as cholesteryl esters (ACBP, ACAT-2 and ACAT-1). The amount of protein is expressed in arbitrary units (a.u.) with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): *, P <0.05; **, P <0.01. For cholesterol diet versus control diet: #, P <0.05; ###, P <0.001.

    Journal:

    Article Title: Liver fatty-acid-binding protein (L-FABP) gene ablation alters liver bile acid metabolism in male mice

    doi: 10.1042/BJ20050296

    Figure Lengend Snippet: Effect of L-FABP gene ablation on liver levels of key proteins involved in uptake, synthesis and storage of bile acid precursor cholesterol Liver homogenates of male mice were separated by SDS/PAGE and electroblotted on to nitrocellulose membranes as described in the Experimental section. The membranes were incubated with polyclonal antisera directed against proteins involved in cholesterol uptake (LDL receptor), efflux (SRB-1), synthesis (HMG-CoA reductase) and storage as cholesteryl esters (ACBP, ACAT-2 and ACAT-1). The amount of protein is expressed in arbitrary units (a.u.) with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): *, P <0.05; **, P <0.01. For cholesterol diet versus control diet: #, P <0.05; ###, P <0.001.

    Article Snippet: Goat polyclonal anti-mouse BSEP (bile salt export pump protein) and goat polyclonal anti-human MRP2 (multidrug resistance associated protein 2) were from Santa Cruz Biotechnology; rabbit polyclonal anti-rat OATP-1 (organic anion transporting polypeptide 1) was from Alpha Diagnostic International (San Antonio, TX, U.S.A.).

    Techniques: Incubation

    Proteins from liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against CYP7A1 (A), CYP27A1 (B) or SCP-x (C) as described in the Experimental section. The amount of protein is expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): **, P<0.01; ***, P<0.001. For cholesterol diet versus control diet: #, P<0.05; and ###, P<0.001.

    Journal:

    Article Title: Liver fatty-acid-binding protein (L-FABP) gene ablation alters liver bile acid metabolism in male mice

    doi: 10.1042/BJ20050296

    Figure Lengend Snippet: Proteins from liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against CYP7A1 (A), CYP27A1 (B) or SCP-x (C) as described in the Experimental section. The amount of protein is expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): **, P<0.01; ***, P<0.001. For cholesterol diet versus control diet: #, P<0.05; and ###, P<0.001.

    Article Snippet: Goat polyclonal anti-mouse BSEP (bile salt export pump protein) and goat polyclonal anti-human MRP2 (multidrug resistance associated protein 2) were from Santa Cruz Biotechnology; rabbit polyclonal anti-rat OATP-1 (organic anion transporting polypeptide 1) was from Alpha Diagnostic International (San Antonio, TX, U.S.A.).

    Techniques: SDS Page, Incubation

    Proteins from liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against cytosolic cholesterol/bile acid transport proteins such as L-FABP (A), SCP-2 (B), caveolin-1 (C), GST (D), or 3α-HSD (E) as described in the Experimental section. The amount of protein was expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): *, P<0.05; **, P<0.01; ***, P<0.001. For cholesterol diet versus control diet: ##, P<0.01; and ###, P<0.001.

    Journal:

    Article Title: Liver fatty-acid-binding protein (L-FABP) gene ablation alters liver bile acid metabolism in male mice

    doi: 10.1042/BJ20050296

    Figure Lengend Snippet: Proteins from liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against cytosolic cholesterol/bile acid transport proteins such as L-FABP (A), SCP-2 (B), caveolin-1 (C), GST (D), or 3α-HSD (E) as described in the Experimental section. The amount of protein was expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): *, P<0.05; **, P<0.01; ***, P<0.001. For cholesterol diet versus control diet: ##, P<0.01; and ###, P<0.001.

    Article Snippet: Goat polyclonal anti-mouse BSEP (bile salt export pump protein) and goat polyclonal anti-human MRP2 (multidrug resistance associated protein 2) were from Santa Cruz Biotechnology; rabbit polyclonal anti-rat OATP-1 (organic anion transporting polypeptide 1) was from Alpha Diagnostic International (San Antonio, TX, U.S.A.).

    Techniques: SDS Page, Incubation

    Proteins from liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against canalicular bile salt translocase proteins such as BSEP (A) and MRP2 (B), or against basolateral/serosal bile salt translocase protein such as OATP-1 (C) as described in the Experimental section. The amount of protein is expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): *, P<0.05; **, P<0.01; ***, P<0.001. For cholesterol diet versus control diet, ###, P<0.001.

    Journal:

    Article Title: Liver fatty-acid-binding protein (L-FABP) gene ablation alters liver bile acid metabolism in male mice

    doi: 10.1042/BJ20050296

    Figure Lengend Snippet: Proteins from liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against canalicular bile salt translocase proteins such as BSEP (A) and MRP2 (B), or against basolateral/serosal bile salt translocase protein such as OATP-1 (C) as described in the Experimental section. The amount of protein is expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): *, P<0.05; **, P<0.01; ***, P<0.001. For cholesterol diet versus control diet, ###, P<0.001.

    Article Snippet: Goat polyclonal anti-mouse BSEP (bile salt export pump protein) and goat polyclonal anti-human MRP2 (multidrug resistance associated protein 2) were from Santa Cruz Biotechnology; rabbit polyclonal anti-rat OATP-1 (organic anion transporting polypeptide 1) was from Alpha Diagnostic International (San Antonio, TX, U.S.A.).

    Techniques: SDS Page, Incubation

    Liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against nuclear regulatory proteins SREBP-1 (A), PPARα (B), FXR (C), LXRα (D) or SHP (E) as described in the Experimental section. The amount of protein is expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): **, P<0.01, ***P<0.001. For cholesterol diet versus control diet: #, P<0.05; ##, P<0.01; and ###, P<0.001.

    Journal:

    Article Title: Liver fatty-acid-binding protein (L-FABP) gene ablation alters liver bile acid metabolism in male mice

    doi: 10.1042/BJ20050296

    Figure Lengend Snippet: Liver homogenates of male mice were separated by SDS/PAGE, electroblotted on to nitrocellulose membranes, and incubated with polyclonal antisera directed against nuclear regulatory proteins SREBP-1 (A), PPARα (B), FXR (C), LXRα (D) or SHP (E) as described in the Experimental section. The amount of protein is expressed in arbitrary units with that present in the control-fed L-FABP (+/+) liver homogenates defined to be 1. The data represent the means±S.E.M. For L-FABP (−/−) versus L-FABP (+/+): **, P<0.01, ***P<0.001. For cholesterol diet versus control diet: #, P<0.05; ##, P<0.01; and ###, P<0.001.

    Article Snippet: Goat polyclonal anti-mouse BSEP (bile salt export pump protein) and goat polyclonal anti-human MRP2 (multidrug resistance associated protein 2) were from Santa Cruz Biotechnology; rabbit polyclonal anti-rat OATP-1 (organic anion transporting polypeptide 1) was from Alpha Diagnostic International (San Antonio, TX, U.S.A.).

    Techniques: SDS Page, Incubation