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Anti-S1PR4 Rabbit Polyclonal Antibody #52525

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Immunocytochemical analysis of S1PR4 staining in HepG2 cells. 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 the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark.
Immunohistochemical analysis of S1PR4 staining in human liver cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Western blotting analysis of S1PR4 expression in HEK293T (A), Hela (B), HepG2 (C), mouse spleen (D) whole cell lysates.
  • 基因名:
    S1PR4
  • 货号:
    52525
  • 应用:
    WB, IHC, IC
  • 物种反应性:
    H
规格:
20 μL,50 μL,100 μL
价格:
¥ 560.00,¥ 1,100.00,¥ 2,000.00
Information
Product Name Anti-S1PR4 Rabbit Polyclonal Antibody
Aliases S1PR4; Sphingosine-1-Phosphate Receptor 4; EDG6; Endothelial Differentiation, Lysophosphatidic Acid G-Protein-Coupled Receptor, 6; Endothelial Differentiation G-Protein Coupled Receptor 6; Sphingosine 1-Phosphate Receptor Edg-6; Sphingosine 1-Phosphate Receptor 4; S1P Receptor Edg-6; S1P Receptor 4; S1P4; Endothelial Differentiation, G-Protein-Coupled Receptor 6; LPC1; SLP4
Background

Gene Name: S1PR4

NCBI Gene Entry: 8698

UniProt Entry: O95977

Application Information

Molecular Weight: Predicted, 41 kDa; observed, 48 kDa

Clonality: Rabbit polyclonal antibody

Species Reactivity: Human

Applications Tested: Western blotting (WB), immunohistochemistry (IHC), immunocytochemistry (IC)

Immunogen A synthesized peptide derived from human S1PR4
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH7.3) containing 30% glycerol, and 0.01% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:500-1:1,000
Immunohistochemistry (IHC): 1:50-1:100
Immunocytochemistry (IC): 1:50-1:200
Note This product is for research use only.
Picture
  • Immunocytochemical analysis of S1PR4 staining in HepG2 cells. 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 the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark.
  • Immunohistochemical analysis of S1PR4 staining in human liver cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
  • Western blotting analysis of S1PR4 expression in HEK293T (A), Hela (B), HepG2 (C), mouse spleen (D) whole cell lysates.
Citation(0)
Immunocytochemical analysis of S1PR4 staining in HepG2 cells. 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 the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark.
Immunohistochemical analysis of S1PR4 staining in human liver cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Western blotting analysis of S1PR4 expression in HEK293T (A), Hela (B), HepG2 (C), mouse spleen (D) whole cell lysates.
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