SGK1 Recombinant Rabbit Monoclonal Antibody [SC05-71]
cat.: ET1610-19
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P, IP, FC
Clonality: Monoclonal
Clone number: SC05-71
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 49 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human SGK1 aa 40-80.
Positive control: Human kidney tissue lysates, human liver tissue, human kidney tissue, mouse liver tissue, mouse brain tissue, mouse kidney tissue, 293.
Subcellular location: Cytoplasm, Nucleus, Cell membrane, Mitochondrion.
Recommended Dilutions:
  WB
  IHC-P
  FC
  IP
1:1,000
1:50-1:200
1:50-1:100
Use at an assay dependent concentration.
Uniprot #: SwissProt: O00141 Human | Q9WVC6 Mouse | Q06226 Rat
Alternative names: OTTHUMP00000017247 Serine/threonine protein kinase SGK Serine/threonine protein kinase Sgk1 Serine/threonine-protein kinase Sgk1 Serum and glucocorticoid regulated kinase Serum/glucocorticoid regulated kinase 1 Serum/glucocorticoid regulated kinase Serum/glucocorticoid-regulated kinase 1 SGK 1 SGK SGK1 Sgk1 variant i3 SGK1_HUMAN
Images
ET1610-19_1.jpg Fig1: Western blot analysis of SGK1 on human kidney tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1610-19, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
ET1610-19_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-SGK1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1610-19, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1610-19_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-SGK1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1610-19, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1610-19_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-SGK1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1610-19, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1610-19_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-SGK1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1610-19, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1610-19_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-SGK1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1610-19, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1610-19_7.jpg Fig7: Flow cytometric analysis of SGK1 was done on 293 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1610-19, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.