Anti-cMet antibody
种属反应性Human, Mouse, Rat
验证应用WB, ICC, IHC-P, FC
抗体类型兔多抗
免疫原Synthetic peptide within mouse cMet aa 650-690.
偶联Non-conjugated
Anti-cMet antibody性能
形态Liquid
浓度1 mg/mL.
存放说明Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
存储缓冲液1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
亚型IgG
纯化方式Peptide affinity purified
亚细胞定位Cell membrane.
其它名称AUTS9 antibody
c met antibody
D249 antibody
Hepatocyte growth factor receptor antibody
HGF antibody
HGF receptor antibody
HGF/SF receptor antibody
HGFR antibody
MET antibody
Met proto oncogene tyrosine kinase antibody
MET proto oncogene, receptor tyrosine kinase antibody
Met proto-oncogene (hepatocyte growth factor receptor) antibody
Met proto-oncogene antibody
Met protooncogene antibody
MET_HUMAN antibody
Oncogene MET antibody
Par4 antibody
Proto-oncogene c-Met antibody
RCCP2 antibody
Scatter factor receptor antibody
SF receptor antibody
Tyrosine-protein kinase Met antibody
more
Anti-cMet antibody应用
WB: 1:1,000
ICC: 1:200
IHC-P: 1:200
FC: 1:100-1:200
Fig1: Western blot analysis of cMet on different cell lysates using anti-cMet antibody at 1/1000 dilution.
Positive control:
Lane 1: Mouse liver
Lane 2: Mouse kidney
Lane 3: D3
Lane 4: MEF
Fig2: ICC staining cMet in N2A cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig3: ICC staining cMet in Hela cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig4: ICC staining cMet in HepG2 cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Fig5: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-cMet antibody. Counter stained with hematoxylin.
Fig6: Immunohistochemical analysis of paraffin-embedded mouse spleen tissue using anti-cMet antibody. Counter stained with hematoxylin.
Fig7: Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-cMet antibody. Counter stained with hematoxylin.
Fig8: Flow cytometric analysis of Hela cells with cMet antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti rabbit IgG (FITC) was used as the secondary antibody.
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