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Tyrosine
Protein Kinase Receptors (Tek, Tie-1, and Tie-2) Antibodies
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Items
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Antigen
peptide
location
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Ab
Host
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Unpurified
Antisera
(100 ul)
Cat #
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Aff. Pure IgG
/Mono
(100 ug)
Cat #
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* Control Peptide
(100 ug)
Cat#
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Tie-1
(Ab#2)
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H, 21aa ~NT
EC domain
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Rb, poly
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TIE12-S
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TIE12-A
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TIE12-P
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Tie-1 |
H, ~740 aa, EC Domain |
m, mono
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TIE13-M |
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Recombinant Human Tie-1, Human
Protein Control
(~1-740 aa EC domain) |
Human Tie-1 protein (inactive)
Control for WB, Cat # TIE12-C (100 ul)
Human Tie-1 protein for ELISA or Standards Cat #
TIE15-R-20 (20 ug) |
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Tie-2
(Ab#2)
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H, 18aa ~NT
EC domain
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Rb
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TIE22-S
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TIE22-A
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TIE22-P
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Tie-2
(Ab#3)
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H, Tie2
~750aa ~EC
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M,
mono
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.
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TIE23-M
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.
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Recombinant Human Tie-2, Human
Protein Control
(~1-744 aa EC domain) |
Human Tie-2 protein (inactive)
Control for WB, Cat # TIE22-C (100 ul)
Human Tie-2 protein for ELISA or Standards Cat #
TIE25-R-20 (20 ug) |
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Tie-2
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M, Tie2
Protein ~EC
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M,
mono
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.
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TIE24-A
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.
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Recombinant Mouse Tie-2,
Human Protein Control
(~1-744 aa EC domain) |
Mouse Tie-2 protein (inactive)
Control for WB, Cat # TIE24-C (100 ul)
Mouse Tie-2 protein for ELISA or Standards Cat #
TIE26-R-20 (20 ug) |
M= Mouse; R=Rat; H=Human; Rb=Rabbit; G=goat; B=Bovine, MO=Monkey; P=pig;
CT= near C-terminus; NT=near N-terminus; Internal=Middle of protein.
EC=extracellular; CP=cytoplasmic domains *
TIEs (Tek) General Information
Embryonic vascular system undergoes a series of complex, highly
regulated series of events involving differentiation, migration and
association of primitive endothelial cells. This process is termed
vasculogenesis. A further remodeling of the primitive vascular system
forms the mature cardiovascular system. This process is known as
angiogenesis (sprouting of new capillary vessels from pre-existing
vasculature). The development of primordia of the heart and large
vessels, primary capillary networks in the embryo and the extraembryonic
structures in the yolk sac. Angiogenesis accounts for the formation of
vasculature into previously avascular organs such as brain and kidney.
Angiogenic activity in the adult is required during the normal tissue
repair, and for the remodeling of the female reproductive organs
(ovulation and placental development). Certain pathological conditions,
such as tumor growth and diabetic retinopathy, also require
angiogenesis. The genetic and molecular mechanism that influence
angiogenesis has only recently begun to be studied and identified. Study
of tumor angiogenesis has led to the identification of several proteins
including basic fibroblast growth factor (bFGF) and vascular endothelial
growth factor. VEGF acts by interacting
with a family of largely endothelial-specific receptor tyrosine kinases
that includes VEGFR-1 (flt-1), VEGFR-2
(flk-1/KDR), and VEGFR-3/Flt-4. Disruption of VEGFRs interferes
with differentiation of endothelial cells and it is lethal for the
embryo.
Another families of receptor tyrosine kinases TIE1
and TIE 2 or Tek have also been identified in vascular
endothelium and hematopoietic cells. Mice lacking TIE 1 or TIE 2 are
lethal. Ties may represent the earliest endothelial cell lineage marker
and may regulate the endothelial cell proliferation, differentiation,
and proper patterning during vasculogenesis. TIEs appear to be acting
downstream of the VEGFRs. In order to delineate the mechanism of actions
of the Tie receptors, novel cloning techniques have been used to
identify their natural ligands.
ADI has produced highly specific antibodies to Ang-1 and Ang-2 and their
receptors (Tie-1 and Tie-2) using specific
peptide sequences. In addition, purified recombinant VEGFs, antibodies
to VEGFs, and their receptors are also available. The control
peptides, used for immunization, are also available to determine
specificity of antibodies.
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