PA1-330

antibody from Invitrogen Antibodies

Targeting: NR1H3 LXR-a, LXRa, RLD-1

Provider product page for PA1-330

Western blot

Immunocytochemistry

Other assay

Antibody data

Antibody Data
Antigen structure
References [8]
Comments [0]
Validations
Western blot [1]
Immunocytochemistry [2]
Other assay [2]

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Product number: PA1-330 - Provider product page
Provider: Invitrogen Antibodies
Product name: LXR alpha Polyclonal Antibody
Antibody type: Polyclonal
Antigen: Synthetic peptide
Description: PA1-330 detects recombinant human liver X receptor (LXR) alpha. This antibody does not detect human recombinant LXR beta protein.
Concentration: 1 mg/mL

NR1H3 protein structure - PA1-330 shown in red.

Submitted references Administration of GDF3 Into Septic Mice Improves Survival via Enhancing LXRα-Mediated Macrophage Phagocytosis.

Wang P, Mu X, Zhao H, Li Y, Wang L, Wolfe V, Cui SN, Wang X, Peng T, Zingarelli B, Wang C, Fan GC
Frontiers in immunology 2021;12:647070

Sectm1a deficiency aggravates inflammation-triggered cardiac dysfunction through disruption of LXRα signalling in macrophages.

Li Y, Deng S, Wang X, Huang W, Chen J, Robbins N, Mu X, Essandoh K, Peng T, Jegga AG, Rubinstein J, Adams DE, Wang Y, Peng J, Fan GC
Cardiovascular research 2021 Feb 22;117(3):890-902

Macrophage miR-34a Is a Key Regulator of Cholesterol Efflux and Atherosclerosis.

Xu Y, Xu Y, Zhu Y, Sun H, Juguilon C, Li F, Fan D, Yin L, Zhang Y
Molecular therapy : the journal of the American Society of Gene Therapy 2020 Jan 8;28(1):202-216

27-hydroxycholesterol decreases cell proliferation in colon cancer cell lines.

Warns J, Marwarha G, Freking N, Ghribi O
Biochimie 2018 Oct;153:171-180

Liver X receptor is a therapeutic target in collagen-induced arthritis.

Chintalacharuvu SR, Sandusky GE, Burris TP, Burmer GC, Nagpal S
Arthritis and rheumatism 2007 Apr;56(4):1365-7

Endotoxin down-regulates ABCG5 and ABCG8 in mouse liver and ABCA1 and ABCG1 in J774 murine macrophages: differential role of LXR.

Khovidhunkit W, Moser AH, Shigenaga JK, Grunfeld C, Feingold KR
Journal of lipid research 2003 Sep;44(9):1728-36

Oxysterol-activated LXRalpha/RXR induces hSR-BI-promoter activity in hepatoma cells and preadipocytes.

Malerød L, Juvet LK, Hanssen-Bauer A, Eskild W, Berg T
Biochemical and biophysical research communications 2002 Dec 20;299(5):916-23

Oxysterol-activated LXRalpha/RXR induces hSR-BI-promoter activity in hepatoma cells and preadipocytes.

Malerød L, Juvet LK, Hanssen-Bauer A, Eskild W, Berg T
Biochemical and biophysical research communications 2002 Dec 20;299(5):916-23

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Supportive validation

Submitted by: Invitrogen Antibodies (provider)
Main image
Experimental details: Western blot analysis was performed on nuclear enriched extracts (30 µg lysate) of MCF7 (Lane 1), THP-1 (Lane 2), A549 (Lane 3), SH-SY5Y (Lane 4), HL-60 (Lane 5) and KARPAS 299 (Lane 6). The blot was probed with Rabbit Anti-LXR alpha Polyclonal Antibody (Product # PA1-330, 2 µg/mL) and detected by chemiluminescence using Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate (Product # A27036, 0.25 µg/mL, 1:4000 dilution). A 50 kDa band corresponding to LXR alpha was observed across the cell lines tested. Known quantity of protein samples were electrophoresed using Novex® NuPAGE® 4-12 % Bis-Tris gel (Product # NP0321BOX), XCell SureLock™ Electrophoresis System (Product # EI0002) and Novex® Sharp Pre-Stained Protein Standard (Product # LC5800). Resolved proteins were then transferred onto a nitrocellulose membrane with iBlot® 2 Dry Blotting System (Product # IB21001). The membrane was probed with the relevant primary and secondary Antibody following blocking with 5 % skimmed milk. Chemiluminescent detection was performed using Pierce™ ECL Western Blotting Substrate (Product # 32106).

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
Main image
Experimental details: Immunofluorescent analysis of LXR alpha (green) showing staining in the nucleus of Hela cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with a LXR alpha polyclonal antibody (Product # PA1-330) in 3% BSA-PBS at a dilution of 1:300 and incubated overnight at 4ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
Main image
Experimental details: Immunofluorescent analysis of LXR alpha (green) showing staining in the nucleus of MCF-7 cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with a LXR alpha polyclonal antibody (Product # PA1-330) in 3% BSA-PBS at a dilution of 1:300 and incubated overnight at 4ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
Main image
Experimental details: NULL

Supportive validation

Submitted by: Invitrogen Antibodies (provider)
Main image
Experimental details: Figure 5 Gene expression profile in BMDMs treated with rGDF3 by high-throughput RNA sequencing. (A) Heatmap of the differentially expressed genes from BMDMs treated with BSA or rGDF3 (20 ng/mL) ( n = 3). (B) The altered expression of CD5L, Bcl2a1b, and MRPS18C gene in rGDF3-treated BMDMs was validated by qRT-PCR ( n = 6). (C) Expression of CD5L and Bcl2a1b in GW3965 (1 mumol/L)-treated BMDMs was determined by qRT-PCR ( n = 6) at 18 h post-treatment. (D) Expression of CD5L and Bcl2a1b in BMDMs were measured at 18 h post-GSK2033 (2 mumol/L) treatment ( n = 6). (E) Graphic scheme of the LXRalpha-CD5L signal cascade in macrophages. Representative images (F) and quantification (G) of immunofluorescence staining for LXRalpha (green) in BMDMs at 18 h after rGDF3 (20 ng/mL) or GW3965 (1 mumol/L) treatment (Scale bar, 10 mum; n = 5). Data are representative of two (B-D,F,G) independent experiments. All results are shown as mean +- SEM and analyzed by Student's t -test (* p < 0.05).