The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/500. Detects a band of approximately 133 kDa (predicted molecular weight: 93 kDa).
Use at an assay dependent concentration.
Inactive tyrosine kinase involved in Wnt signaling pathway. Component of both the non-canonical (also known as the Wnt/planar cell polarity signaling) and the canonical Wnt signaling pathway. Functions in cell adhesion, cell migration, cell polarity, proliferation, actin cytoskeleton reorganization and apoptosis. Has a role in embryogenesis, epithelial tissue organization and angiogenesis.
Highly expressed in lung, liver, pancreas, kidney, placenta and melanocytes. Weakly expressed in thyroid gland, ovary, brain, heart and skeletal muscle. Also expressed in erythroleukemia cells. But not expressed in colon.
Belongs to the protein kinase superfamily. Tyr protein kinase family. Insulin receptor subfamily. Contains 7 Ig-like C2-type (immunoglobulin-like) domains. Contains 1 protein kinase domain.
The protein kinase domain is predicted to be catalytically inactive.
MMP14 cleaves PTK7 between Pro-621 and Leu-622 generating an N-terminal soluble (70 kDa) fragment and a membrane C-terminal (50 kDa) fragment. Proteolysis by MMP14 regulates PTK7 function in non-canonical Wnt signaling pathway.
Membrane. Cell junction. Colocalizes with MMP14 at cell junctions. Also localizes at the leading edge of migrating cells.
Human colon carcinoma kinase 4 (CCK4) mRNA complete cds antibody
Inactive tyrosine-protein kinase 7 antibody
Protein tyrosine kinase PTK 7 antibody
Protein-tyrosine kinase 7 antibody
Pseudo tyrosine kinase receptor 7 antibody
PTK 7 antibody
PTK7 protein tyrosine kinase 7 antibody
PTK7 protein tyrosine kinase antibody
Serum response factor antibody
Tyrosine-protein kinase-like 7 antibody
Anti-CCK4 antibody images
Immunocytochemistry/ Immunofluorescence - Anti-CCK4 antibody (ab117412)This image is courtesy of an anonymous Abreview
ab117412 staining CCK4 (green) in wild type mouse embryonic stem cells (D3) by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with methanol/acetone (1:1), permeabilized with 0.1% Triton X-100 and blocked with 1% serum for 30 minutes at 16°C. Samples were incubated with primary antibody (1/100 in blocking buffer) for 2 hour at 16°C. ab15007, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG polyclonal (1/200) was used as the secondary antibody. DAPI (blue) - nuclei.