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Vee Gee Microscope Objective, 40x Achromatic (DIN)/0.65 N.A.

Vee Gee Scientific API ASTM 54H Hydrometers with SafetyBLUE F Thermometer, 29 to 41 API

Vee Gee Scientific Microscope Fuse, 0.75A / 250V, for 1250s, 1260s, 1270ZFs, 1270ZHs, 1130s

Vee Gee Scientific Microscope Fuse, 1270ZLs, 1250SLs, 1130ZLs, Newer 1490s

Vee Gee Scientific Microscope Fuse, 5.0A / 250V, for 1282ECM and 1286ECM External Power Supply

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 10 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 10 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 100 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 100 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 1000 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 1000 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 200 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 200 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 2000 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 2000 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 25 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 25 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 250 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 250 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 5 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 5 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 50 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 50 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 500 mL

Vee Gee SIBATA Class A Volumetric Flasks with Glass Stopper, To Contain, 500 mL

Veegum(R) HV, Granular

Veegum(R) HV, Granular

Veegum(R) HV, Granular

Veegum(R) R

Veegum(R) R

Veegum(R) R

Veegum(R) R

VEGETABLE OIL HYDROGENATED

Monoclonal Antibodies

Monoclonal Antibodies

Polyclonal Antibodies

Polyclonal Antibodies

Polyclonal Antibodies

Polyclonal Antibodies

Polyclonal Antibodies

Polyclonal Antibodies

Vascular Endothelial Growth Factor (VEGF) was initially purified from media conditioned by normal bovine pituitary folliculo-stellate cells and by a variety of transformed cell lines as a mitogen specific for vascular endothelial cells. It was subsequently found to be identical to an independently discovered vascular permeability factor (VPF), which was previously identified in media conditioned by tumor cell lines based on its ability to increase the permeability of capillary blood vessels. Three mouse cDNA clones, which arise through alternative splicing and which encode mature mouse monomeric VEGF having 120, 164, or 188, amino acids, respectively, have been identified. Two receptor tyrosine kinases (RTKs), Flt-1 and Flk-1 (the mouse homologue of human KDR), both members of the type III subclass of RTKs containing seven immunoglobulin-like repeats in their extracellular domains, have been shown to bind VEGF with high affinity. The roles of the homodimers of KDR, Flt, and the heterodimer of KDR/Flt in VEGF signal transduction remain to be elucidated. In vivo, VEGF has been found to be a potent angiogenesis inducer.

Vascular Endothelial Growth Factor (VEGF) was initially purified from media conditioned by normal bovine pituitary folliculo-stellate cells and by a variety of transformed cell lines as a mitogen specific for vascular endothelial cells. It was subsequently found to be identical to an independently discovered vascular permeability factor (VPF), which was previously identified in media conditioned by tumor cell lines based on its ability to increase the permeability of capillary blood vessels. Three mouse cDNA clones, which arise through alternative splicing and which encode mature mouse monomeric VEGF having 120, 164, or 188, amino acids, respectively, have been identified. Two receptor tyrosine kinases (RTKs), Flt-1 and Flk-1 (the mouse homologue of human KDR), both members of the type III subclass of RTKs containing seven immunoglobulin-like repeats in their extracellular domains, have been shown to bind VEGF with high affinity. The roles of the homodimers of KDR, Flt, and the heterodimer of KDR/Flt in VEGF signal transduction remain to be elucidated. In vivo, VEGF has been found to be a potent angiogenesis inducer.

Vascular Endothelial Growth Factor (VEGF) was initially purified from media conditioned by normal bovine pituitary folliculo-stellate cells and by a variety of transformed cell lines as a mitogen specific for vascular endothelial cells. It was subsequently found to be identical to an independently discovered vascular permeability factor (VPF), which was previously identified in media conditioned by tumor cell lines based on its ability to increase the permeability of capillary blood vessels. Three mouse cDNA clones, which arise through alternative splicing and which encode mature mouse monomeric VEGF having 120, 164, or 188, amino acids, respectively, have been identified. Two receptor tyrosine kinases (RTKs), Flt-1 and Flk-1 (the mouse homologue of human KDR), both members of the type III subclass of RTKs containing seven immunoglobulin-like repeats in their extracellular domains, have been shown to bind VEGF with high affinity. The roles of the homodimers of KDR, Flt, and the heterodimer of KDR/Flt in VEGF signal transduction remain to be elucidated. In vivo, VEGF has been found to be a potent angiogenesis inducer.

Vascular endothelial growth factor C (VEGF-C) is a member of the platelet-derived growth factor/vascular endothelial growth factor (PDGF/VEGF) family, is active in angiogenesis, lymphangiogenesis and endothelial cell growth and survival, and can also affect the permeability of blood vessels. VEGF-C is expressed in various tissues, however it is not produced in peripheral blood lymphocytes. It forms cell surface-associated non-covalent disulfide linked homodimers, and can bind and activate both VEGFR-2 (flk1) and VEGFR-3 (flt4) receptors. The structure and function of VEGF-C is similar to those of vascular endothelial growth factor D (VEGF-D).

Vascular endothelial growth factor C (VEGF-C) is a member of the platelet-derived growth factor/vascular endothelial growth factor (PDGF/VEGF) family, is active in angiogenesis, lymphangiogenesis and endothelial cell growth and survival, and can also affect the permeability of blood vessels. VEGF-C is expressed in various tissues, however it is not produced in peripheral blood lymphocytes. It forms cell surface-associated non-covalent disulfide linked homodimers, and can bind and activate both VEGFR-2 (flk1) and VEGFR-3 (flt4) receptors. The structure and function of VEGF-C is similar to those of vascular endothelial growth factor D (VEGF-D).

Vascular endothelial growth factor C (VEGF-C) is a member of the platelet-derived growth factor/vascular endothelial growth factor (PDGF/VEGF) family, is active in angiogenesis, lymphangiogenesis and endothelial cell growth and survival, and can also affect the permeability of blood vessels. VEGF-C is expressed in various tissues, however it is not produced in peripheral blood lymphocytes. It forms cell surface-associated non-covalent disulfide linked homodimers, and can bind and activate both VEGFR-2 (flk1) and VEGFR-3 (flt4) receptors. The structure and function of VEGF-C is similar to those of vascular endothelial growth factor D (VEGF-D).

Monoclonal Antibodies

Monoclonal Antibodies

Polyclonal Antibodies