MUC4 Recombinant Rabbit Monoclonal Antibody [JM19-36]
cat.: ET1705-13
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Rat
Applications: WB, IHC-P, FC
Clonality: Monoclonal
Clone number: JM19-36
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: 542 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human MUC4 aa 1,564-1,673 / 2,169.
Positive control: Rat brain tissue, human lung carcinoma tissue, human colon tissue, human stomach carcinoma tissue, A549.
Subcellular location: Secreted, Cell membrane and Membrane.
Recommended Dilutions:
  WB
  IHC-P
  FC

1:500
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: Q99102 Human
Alternative names: Ascites sialoglycoprotein 1 Ascites sialoglycoprotein 2 Ascites sialoglycoprotein ASGP ASGP-1 ASGP-2 HSA276359 MUC 4 MUC-4 Muc4 MUC4_HUMAN Mucin 4 Mucin 4 cell surface associated Mucin 4 tracheobronchial Mucin-4 beta chain Pancreatic adenocarcinoma mucin Testis mucin Tracheobronchial mucin Tracheobronchial mucin Fragment
Images
ET1705-13_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-MUC4 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-13, 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.
ET1705-13_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue using anti-MUC4 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-13, 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.
ET1705-13_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-MUC4 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-13, 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.
ET1705-13_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human stomach carcinoma tissue using anti-MUC4 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-13, 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.
ET1705-13_5.jpg Fig5: Flow cytometric analysis of MUC4 was done on A549 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1705-13, 1/50) (red). After incubation of the primary antibody at room temperature for an 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.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”.