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AB228949

Anti-Bile Acid Receptor NR1H4 抗体

Anti-Bile Acid Receptor NR1H4 antibody

  • JP Deleterious:医薬用外劇物

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(4 Publications)

Rabbit Polyclonal Bile Acid Receptor NR1H4 antibody. Suitable for IHC-P, WB and reacts with Mouse, Rat, Human samples. Cited in 4 publications. Immunogen corresponding to Recombinant Fragment Protein within Human NR1H4.

別名を表示する

BAR, FXR, HRR1, RIP14, NR1H4, Bile acid receptor, Farnesoid X-activated receptor, Farnesol receptor HRR-1, Nuclear receptor subfamily 1 group H member 4, Retinoid X receptor-interacting protein 14, RXR-interacting protein 14

3 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bile Acid Receptor NR1H4 antibody (AB228949)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bile Acid Receptor NR1H4 antibody (AB228949)

Immunohistochemical analysis of mouse tissues stained for NR1H4 protein with ab228949 at a 1/500 dilution.

Antigen retrieval : Citrate buffer, pH 6.0, 15 min.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bile Acid Receptor NR1H4 antibody (AB228949)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bile Acid Receptor NR1H4 antibody (AB228949)

Immunohistochemical analysis of rat tissues stained for NR1H4 protein with ab228949 at a 1/500 dilution.

Antigen retrieval : Citrate buffer, pH 6.0, 15 min.

Western blot - Anti-Bile Acid Receptor NR1H4 antibody (AB228949)
  • WB

Supplier Data

Western blot - Anti-Bile Acid Receptor NR1H4 antibody (AB228949)

Samples were separated by 10% SDS PAGE.

All lanes:

Western blot - Anti-Bile Acid Receptor NR1H4 antibody (ab228949) at 1/500 dilution

Lane 1:

293T whole cell lysates at 30 µg

Lane 2:

A431 whole cell lysates at 30 µg

Lane 3:

HeLa whole cell lysates at 30 µg

Lane 4:

HepG2 whole cell lysates at 30 µg

Secondary

All lanes:

HRP-conjugated anti-rabbit IgG antibody

Predicted band size: 56 kDa

false

Key facts

宿主種

Rabbit

クローン性

Polyclonal

アイソタイプ

IgG

キャリアフリー

No

交差種

Mouse, Rat, Human

アプリケーション

WB, IHC-P

applications

免疫原

Recombinant Fragment Protein within Human NR1H4. The exact immunogen used to generate this antibody is proprietary information.

Q96RI1

Reactivity data

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出荷温度及び保存条件

製品の状態
Liquid
精製方法
Affinity purification Immunogen
バッファー組成
pH: 7 Preservative: 0.01% Thimerosal (merthiolate) Constituents: PBS, 20% Glycerol (glycerin, glycerine), 1% BSA
出荷温度
Blue Ice
短期保存期間
1-2 weeks
短期保存温度
+4°C
長期保存温度
-20°C
分注に関する情報
Upon delivery aliquot
保管に関する情報
Avoid freeze / thaw cycle

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

Bile Acid Receptor NR1H4 also known as Farnesoid X Receptor (FXR) is a nuclear receptor with a mass of approximately 57 kDa. It functions as a transcription factor regulating the expression of genes involved in bile acid lipid and glucose homeostasis. NR1H4 is expressed mainly in the liver intestines kidneys and adrenal glands where it plays a critical role in maintaining metabolic balance. By binding bile acids NR1H4 activates allowing it to bind to DNA and modulate gene expression.
Biological function summary

NR1H4 influences the body's metabolism by controlling genes responsible for bile acid synthesis conjugation and transport. It forms a heterodimer with Retinoid X Receptor (RXR) to regulate these processes. As an important regulator NR1H4 controls the enterohepatic circulation of bile acids reducing toxicity by lowering hepatic bile acid production. Additionally it influences lipid and glucose metabolism linking it to broader metabolic functions.

Pathways

NR1H4 is involved in the bile acid signaling and lipid metabolism pathways. Within the bile acid signaling pathway NR1H4 modulates the interaction with various proteins such as Small Heterodimer Partner (SHP) to suppress bile acid synthesis. In the context of lipid metabolism NR1H4 interacts with Liver X Receptor (LXR) to regulate cholesterol and triglyceride levels. These interactions demonstrate NR1H4's integral role in maintaining lipid homeostasis.

NR1H4 bears relevance to cholestatic liver disease and nonalcoholic fatty liver disease (NAFLD). In cholestatic liver disease impaired NR1H4 function leads to abnormal bile acid regulation contributing to liver damage. In NAFLD altered NR1H4 activity affects lipid metabolism promoting liver steatosis. Through these diseases NR1H4 shares connections with the CYP7A1 protein critical for bile acid synthesis and the Peroxisome Proliferator-Activated Receptor Alpha (PPARα) involved in lipid oxidation.

製品プロトコール

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ターゲットの情報

Ligand-activated transcription factor. Receptor for bile acids (BAs) such as chenodeoxycholic acid (CDCA), lithocholic acid, deoxycholic acid (DCA) and allocholic acid (ACA). Plays a essential role in BA homeostasis through the regulation of genes involved in BA synthesis, conjugation and enterohepatic circulation. Also regulates lipid and glucose homeostasis and is involved innate immune response (PubMed : 10334992, PubMed : 10334993, PubMed : 21383957, PubMed : 22820415). The FXR-RXR heterodimer binds predominantly to farnesoid X receptor response elements (FXREs) containing two inverted repeats of the consensus sequence 5'-AGGTCA-3' in which the monomers are spaced by 1 nucleotide (IR-1) but also to tandem repeat DR1 sites with lower affinity, and can be activated by either FXR or RXR-specific ligands. It is proposed that monomeric nuclear receptors such as NR5A2/LRH-1 bound to coregulatory nuclear responsive element (NRE) halfsites located in close proximity to FXREs modulate transcriptional activity (By similarity). In the liver activates transcription of the corepressor NR0B2 thereby indirectly inhibiting CYP7A1 and CYP8B1 (involved in BA synthesis) implicating at least in part histone demethylase KDM1A resulting in epigenomic repression, and SLC10A1/NTCP (involved in hepatic uptake of conjugated BAs). Activates transcription of the repressor MAFG (involved in regulation of BA synthesis) (By similarity). Activates transcription of SLC27A5/BACS and BAAT (involved in BA conjugation), ABCB11/BSEP (involved in bile salt export) by directly recruiting histone methyltransferase CARM1, and ABCC2/MRP2 (involved in secretion of conjugated BAs) and ABCB4 (involved in secretion of phosphatidylcholine in the small intestine) (PubMed : 12754200, PubMed : 15471871, PubMed : 17895379). Activates transcription of SLC27A5/BACS and BAAT (involved in BA conjugation), ABCB11/BSEP (involved in bile salt export) by directly recruiting histone methyltransferase CARM1, and ABCC2/MRP2 (involved in secretion of conjugated BAs) and ABCB4 (involved in secretion of phosphatidylcholine in the small intestine) (PubMed : 10514450, PubMed : 15239098, PubMed : 16269519). In the intestine activates FGF19 expression and secretion leading to hepatic CYP7A1 repression (PubMed : 12815072, PubMed : 19085950). The function also involves the coordinated induction of hepatic KLB/beta-klotho expression (By similarity). Regulates transcription of liver UGT2B4 and SULT2A1 involved in BA detoxification; binding to the UGT2B4 promoter seems to imply a monomeric transactivation independent of RXRA (PubMed : 12806625, PubMed : 16946559). Modulates lipid homeostasis by activating liver NR0B2/SHP-mediated repression of SREBF1 (involved in de novo lipogenesis), expression of PLTP (involved in HDL formation), SCARB1 (involved in HDL hepatic uptake), APOE, APOC1, APOC4, PPARA (involved in beta-oxidation of fatty acids), VLDLR and SDC1 (involved in the hepatic uptake of LDL and IDL remnants), and inhibiting expression of MTTP (involved in VLDL assembly (PubMed : 12554753, PubMed : 12660231, PubMed : 15337761). Increases expression of APOC2 (promoting lipoprotein lipase activity implicated in triglyceride clearance) (PubMed : 11579204). Transrepresses APOA1 involving a monomeric competition with NR2A1 for binding to a DR1 element (PubMed : 11927623, PubMed : 21804189). Also reduces triglyceride clearance by inhibiting expression of ANGPTL3 and APOC3 (both involved in inhibition of lipoprotein lipase) (PubMed : 12891557). Involved in glucose homeostasis by modulating hepatic gluconeogenesis through activation of NR0B2/SHP-mediated repression of respective genes. Modulates glycogen synthesis (inducing phosphorylation of glycogen synthase kinase-3) (By similarity). Modulates glucose-stimulated insulin secretion and is involved in insulin resistance (PubMed : 20447400). Involved in intestinal innate immunity. Plays a role in protecting the distal small intestine against bacterial overgrowth and preservation of the epithelial barrier (By similarity). Down-regulates inflammatory cytokine expression in several types of immune cells including macrophages and mononuclear cells (PubMed : 21242261). Mediates trans-repression of TLR4-induced cytokine expression; the function seems to require its sumoylation and prevents N-CoR nuclear receptor corepressor clearance from target genes such as IL1B and NOS2 (PubMed : 19864602). Involved in the TLR9-mediated protective mechanism in intestinal inflammation. Plays an anti-inflammatory role in liver inflammation; proposed to inhibit pro-inflammatory (but not antiapoptotic) NF-kappa-B signaling) (By similarity).. Isoform 1. Promotes transcriptional activation of target genes NR0B2/SHP (inducible by unconjugated CDCA), SLC51B/OSTB (inducible by unconjugated CDCA and DCA) and FABP6/IBAP; low activity for ABCB11/BSEP (inducible by unconjugated CDCA, DCA and ACA); not inducible by taurine- and glycine-amidated CDCA.. Isoform 2. Promotes transcriptional activation of target genes ABCB11/BSEP (inducible by unconjugated CDCA, DCA and ACA), NR0B2/SHP (inducible by unconjugated CDCA DCA and ACA), SLC51B/OSTB (inducible by unconjugated CDCA and DCA) and FABP6/IBAP; not inducible by taurine- and glycine-amidated CDCA.. Isoform 3. Promotes transcriptional activation of target genes NR0B2/SHP (inducible by unconjugated CDCA), SLC51B/OSTB (inducible by unconjugated CDCA and DCA) and IBAP; low activity for ABCB11/BSEP (inducible by unconjugated CDCA, DCA and ACA); not inducible by taurine- and glycine-amidated CDCA.. Isoform 4. Promotes transcriptional activation of target genes ABCB11/BSEP (inducible by unconjugated CDCA, ACA and DCA), NR0B2/SHP (inducible by unconjugated CDCA, ACA and DCA), SLC51B/OSTB (inducible by unconjugated CDCA and DCA) and FABP6/IBAP; most efficient isoform compared to isoforms 1 to 3; not inducible by taurine- and glycine-amidated CDCA.
See full target information NR1H4

文献 (4)

Recent publications for all applications. Explore the full list and refine your search

Journal of dairy science 107:8629-8641 PubMed38825110

2024

Expression of hepatic genes involved in bile acid metabolism in dairy cows with fatty liver.

Applications

Unspecified application

Species

Unspecified reactive species

Xiliang Du,Mingchao Liu,Erminio Trevisi,Lingxue Ju,Yuting Yang,Wenwen Gao,Yuxiang Song,Lin Lei,Majigsuren Zolzaya,Xinwei Li,Zhiyuan Fang,Guowen Liu

Gut microbes 16:2310277 PubMed38332701

2024

Vancomycin relieves tacrolimus-induced hyperglycemia by eliminating gut bacterial beta-glucuronidase enzyme activity.

Applications

Unspecified application

Species

Unspecified reactive species

Peixia Li,Rui Zhang,Jinping Zhou,Pengpeng Guo,Yani Liu,Shaojun Shi

Nature communications 14:6908 PubMed37903763

2023

Farnesoid X receptor activation by bile acids suppresses lipid peroxidation and ferroptosis.

Applications

Unspecified application

Species

Unspecified reactive species

Juliane Tschuck,Lea Theilacker,Ina Rothenaigner,Stefanie A I Weiß,Banu Akdogan,Van Thanh Lam,Constanze Müller,Roman Graf,Stefanie Brandner,Christian Pütz,Tamara Rieder,Philippe Schmitt-Kopplin,Michelle Vincendeau,Hans Zischka,Kenji Schorpp,Kamyar Hadian

World journal of gastroenterology 26:3586-3602 PubMed32742128

2020

TBL1XR1 induces cell proliferation and inhibit cell apoptosis by the PI3K/AKT pathway in pancreatic ductal adenocarcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Jian-Feng Gu,Wei Fu,Hai-Xin Qian,Wen-Xiu Gu,Yang Zong,Qian Chen,Long Lu
View all publications

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