Mammaglobin A Mouse Monoclonal Antibody [A9A3]
cat.: HA601089
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human
Applications: IHC-P
Clonality: Monoclonal
Clone number: A9A3
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 10 kDa
Isotype: IgG1
Immunogen: Synthetic peptide within Human Mammaglobin A aa 21-70 / 93.
Positive control: Human skin tissue, human breast tissue.
Subcellular location: Secreted.
Recommended Dilutions:
  IHC-P

1:800-1:1,000
Uniprot #: SwissProt: Q13296 Human
Alternative names: Mammaglobin 1 Mammaglobin-1 Mammaglobin-A MGB1 Scgb2a2 Secretoglobin family 2A member 2 SG2A2 SG2A2_HUMAN UGB2
Images
HA601089_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human skin tissue with Mouse anti-Mammaglobin A antibody (HA601089) at 1/800 dilution.

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 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA601089) at 1/800 dilution for 1 hour 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.
HA601089_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human breast tissue with Mouse anti-Mammaglobin A antibody (HA601089) at 1/1,000 dilution.

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 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA601089) at 1/1,000 dilution for 1 hour 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.