c-Met Mouse Monoclonal Antibody [A9A5]
cat.: HA601093
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: A9A5
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: 156 kDa
Isotype: IgG1
Immunogen: Synthetic peptide within Human c-Met aa 1,341-1,390 / 1,390.
Positive control: A549 cell lysate, HepG2 cell lysate, human lung carcinoma tissue.
Subcellular location: Membrane; Secreted.
Recommended Dilutions:
  WB
  IHC-P

1:500
1:400
Uniprot #: SwissProt: P08581 Human
Alternative names: Hepatocyte growth factor receptor EC:2.7.10.1 HGF receptor HGF/SF receptor Proto-oncogene c-Met Scatter factor receptor (SF receptor) Tyrosine-protein kinase Met
Images
HA601093_1.jpg Fig1: Western blot analysis of c-Met on different lysates with Mouse anti-c-Met antibody (HA601093) at 1/500 dilution.

Lane 1: A549 cell lysate
Lane 2: HepG2 cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 156 kDa
Observed band size: 130 kDa

Exposure time: 2 minutes;

6% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA601093) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:150,000 dilution was used for 1 hour at room temperature.
HA601093_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue with Mouse anti-c-Met antibody (HA601093) at 1/400 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 (HA601093) at 1/400 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”.