Rat Anti-FLT4 Recombinant Antibody (5F63) (CBMAB-V0091-LY)

Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Cellular response to vascular endothelial growth factor stimulus Source: UniProtKB
Hematopoietic progenitor cell differentiation Source: GO_Central
Lung alveolus development Source: Ensembl
Lymphangiogenesis Source: UniProtKB
Lymph vessel development Source: BHF-UCL
Negative regulation of apoptotic process Source: UniProtKB
Peptidyl-tyrosine phosphorylation Source: UniProtKB
Positive regulation of cell population proliferation Source: UniProtKB
Positive regulation of endothelial cell migration Source: UniProtKB
Positive regulation of endothelial cell proliferation Source: UniProtKB
Positive regulation of ERK1 and ERK2 cascade Source: UniProtKB
Positive regulation of JNK cascade Source: UniProtKB
Positive regulation of kinase activity Source: GO_Central
Positive regulation of MAPK cascade Source: UniProtKB
Positive regulation of protein kinase C signaling Source: UniProtKB
Positive regulation of protein phosphorylation Source: UniProtKB
Positive regulation of vascular endothelial growth factor production Source: UniProtKB
Protein autophosphorylation Source: UniProtKB
Regulation of blood vessel remodeling Source: UniProtKB
Respiratory system process Source: Ensembl
Sprouting angiogenesis Source: UniProtKB
Transmembrane receptor protein tyrosine kinase signaling pathway Source: GO_Central
Vascular endothelial growth factor receptor signaling pathway Source: MGI
Vascular endothelial growth factor signaling pathway Source: UniProtKB
Vasculature development Source: UniProtKB
Isoform 1&2: Cell membrane. Ligand-mediated autophosphorylation leads to rapid internalization.
Isoform 3: Cytoplasm; Secreted
A form of primary lymphedema, a disease characterized by swelling of body parts due to developmental anomalies and functional defects of the lymphatic system. Patients with lymphedema may suffer from recurrent local infections. LMPHM1 is an autosomal dominant form with variable expression and severity. Onset is usually at birth or in early childhood but can occur later. Affected individuals manifest lymphedema, predominantly in the lower limbs, and hypoplasia of lymphatic vessels. Additional features are hemangioma and nail dysplasia or papillomatosis.
Hemangioma, capillary infantile (HCI):
A condition characterized by dull red, firm, dome-shaped hemangiomas, sharply demarcated from surrounding skin, usually presenting at birth or occurring within the first two or three months of life. They result from highly proliferative, localized growth of capillary endothelium and generally undergo regression and involution without scarring.
Congenital heart defects, multiple types, 7 (CHTD7):
An autosomal dominant disorder with incomplete penetrance characterized by congenital developmental abnormalities involving structures of the heart. Common defects include tetralogy of Fallot, pulmonary stenosis or atresia, absent pulmonary valve, right aortic arch, double aortic arch, and major aortopulmonary collateral arteries.
Helical: 776-796
Cytoplasmic: 797-1363
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols
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Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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