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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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TEK / TIE2 Antibody (phospho‑Tyr992) LS‑C152798
TIE2 antibody LS-C152798 is an unconjugated rabbit polyclonal antibody to human TIE2 (TEK). Validated for IHC, IP and WB.
Catalog
Size
Price
LS-C152798-100
100 µg
Unavailable

Popular TEK / TIE2 Products

Antibody
Species: Human
Applications: IHC, IHC - Paraffin, IHC - Frozen, Western blot
Antibody
Species: Human
Applications: Western blot, ELISA
Antibody
Species: Mouse, Human
Applications: IHC, IHC - Frozen, Flow Cytometry
Two-color surface staining of mouse bone marrow with 1 ug PE anti-mouse CD202b (TEK4) and APC Sca-1 (D7) (LS-C107045) + APC CD117/c-Kit (2B8) (LS-C107024). Total viable lineage negative cells were used for analysis. This image was taken for the unconjugated form of this product. Other forms have not been tested.
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Product Description

TIE2 antibody LS-C152798 is an unconjugated rabbit polyclonal antibody to human TIE2 (TEK). Validated for IHC, IP and WB.
About TEK / TIE2
Tyrosine-protein kinase that acts as cell-surface receptor for ANGPT1, ANGPT2 and ANGPT4 and regulates angiogenesis, endothelial cell survival, proliferation, migration, adhesion and cell spreading, reorganization of the actin cytoskeleton, but also maintenance of vascular quiescence. Has anti-inflammatory effects by preventing the leakage of proinflammatory plasma proteins and leukocytes from blood vessels. Required for normal angiogenesis and heart development during embryogenesis. Q02763 NM_000459 NP_000450.2

TEK Antibody, Angiopoietin-1 receptor Antibody, CD202b antigen Antibody, CD202B Antibody, Endothelial tyrosine kinase Antibody, HTIE2 Antibody, Hyk Antibody, Soluble TIE2 variant 1 Antibody, Soluble TIE2 variant 2 Antibody, TIE-2 Antibody, TIE2 Antibody, VMCM Antibody, Tek tyrosine kinase Antibody, VMCM1 Antibody, p140 TEK Antibody


Specifications

Target
Human TEK / TIE2
Host
Rabbit
Reactivity
Human (tested or 100% immunogen sequence identity)
Clonality
IgG Polyclonal
Conjugations
Unconjugated
Purification
Affinity purified
Modifications
Unmodified
Applications
  • IHC
  • Western blot
  • Immunoprecipitation
Performing IHC? See our complete line of Immunohistochemistry Reagents including antigen retrieval solutions, blocking agents ABC Detection Kits and polymers, biotinylated secondary antibodies, substrates and more.
Immunogen
TEK / TIE2 antibody was raised against synthetic peptide encompassing and including phosphorylated Tyr992 of human TIE2
Epitope
pTyr992
Specificity
Recognizes TIE2/TEK phosphorylated on Tyr992
Presentation
PBS, 0.05% sodium azide in 50% glycerol
Storage
Store at -20°C. Aliquot to avoid freeze-thaw cycles. Store undiluted.
Restrictions
For research use only.
Guarantee
This antibody carries the LSBio 100% Guarantee.

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Images


Western blot

WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.
WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.

Western blot

WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.
WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.

Western blot

WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.
WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.

Western blot

WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.
WB: Untreated and pervanadate-treated HUVEC (lanes 1 and 2, respectively) were resolved by SDS-PAGE, transferred to PVDF (Immobilon-P), and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated HUVEC lysate was either unblocked, TIE2 Tyr992 phosphorylated-peptide blocked, or TIE2 non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-TIE2 (Tyr992) (1:1,000). Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated TIE2.


Requested From: 
Date Requested: 6/24/2018

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