p40-phox Recombinant Rabbit Monoclonal Antibody [JE58-57]
cat.: HA720040
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P, FC
Clonality: Monoclonal
Clone number: JE58-57
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. 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: 39 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human p40-phox aa 290-339/339.
Positive control: Daudi cell lysate, THP-1 cell lysate, human colon tissue, human spleen tissue, THP-1.
Subcellular location: Endosome membrane, Cytosol, Membrane.
Recommended Dilutions:
  WB
  IHC-P
  FC

1:500-1:2,000
1:50-1:200
1:500-1:1,000
Uniprot #: SwissProt: Q15080 Human
Alternative names: CGD3 MGC3810 NCF 4 NCF NCF-4 Ncf4 NCF4_HUMAN Neutrophil cytosol factor 4 Neutrophil cytosolic factor 4 Neutrophil NADPH oxidase factor 4 p40-phox p40phox SH3 and PX domain-containing protein 4 SH3PXD4
Images
HA720040_1.jpg Fig1: Western blot analysis of p40-phox on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (HA720040, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: Daudi cell lysate
Lane 2: THP-1 cell lysate
HA720040_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-p40-phox 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 (HA720040, 1/200) 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.
HA720040_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-p40-phox 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 (HA720040, 1/200) 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.
HA720040_4.jpg Fig4: Flow cytometric analysis of p40-phox was done on THP-1 cells. The cells were fixed, permeabilized and stained with the primary antibody (HA720040, 1ug/ml) (red) compared with Rabbit IgG, monoclonal - Isotype Control (green). After incubation of the primary antibody at +4℃ for 1 hour, the cells were stained with a Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃ (dark incubation).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”.