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Anti-c-Met (Phospho-Y1349) Antibody

Catalog Number: orb393106

DispatchUsually dispatched within 5-10 working days
$ 160.00
Catalog Numberorb393106
CategoryAntibodies
DescriptionRabbit polyclonal antibody to MET (Phospho-Y1349)
Species/HostRabbit
ClonalityPolyclonal
Tested applicationsIF, IH, WB
ReactivityHuman, Mouse, Porcine, Rat
ImmunogenKLH-conjugated synthetic phosphopeptide corresponding to residues surrounding Y1349 of human c-Met protein. The exact sequence is proprietary.
Dilution rangeWB: 1:500:1000
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
ConjugationUnconjugated
TargetMET
Entrez24553, 4233
UniProt IDP08581, P97523, P16056
SourceRabbit
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Alternative namesanti-AUTS9 antibody, anti-c met antibody, anti-D24
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NoteFor research use only
Expiration Date12 months from date of receipt.
Anti-c-Met (Phospho-Y1349) Antibody

Western blot analysis of c-Met (Phospho-Y1349) expression in CT26 (A), rat liver (B), HEK293T (C), LO2 (D) whole cell lysates. (Predicted band size: 155 kD; Observed band size: 145; 170 kD)

Anti-c-Met (Phospho-Y1349) Antibody

Immunohistochemical analysis of c-Met (Phospho-Y1349) staining in human colorectal cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (Phospho-H 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Anti-c-Met (Phospho-Y1349) Antibody

Immunofluorescent analysis of c-Met (Phospho-Y1349) staining in LO2 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).