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AB307557

Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free

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Rabbit Recombinant Monoclonal TIE2 antibody. Carrier free. Suitable for WB and reacts with Mouse, Human samples.

View Alternative Names

CD202b, TIE2, VMCM, VMCM1, TEK, Angiopoietin-1 receptor, Endothelial tyrosine kinase, Tunica interna endothelial cell kinase, Tyrosine kinase with Ig and EGF homology domains-2, Tyrosine-protein kinase receptor TEK, Tyrosine-protein kinase receptor TIE-2, p140 TEK, hTIE2

5 Images
Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)
  • WB

Supplier Data

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)

This data was developed using 307556, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

TIE 2 is specifically expressed in endothelial cells and their progenitors (PMID : 8386827; PMID : 1630810; PMID : 8382358).

Negative control : HEK-293 (PMID : 17189382; PMID : 15851516).

The identity of the bands at approximately 60 kDa and 37 kDa is unknown.

This blot was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.

All lanes:

Western blot - Anti-TIE2 antibody [EPR26540-78] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr26540-78-ab307556'>ab307556</a>) at 1/1000 dilution

Lane 1:

HUVEC (human umbilical vein endothelial cell) whole cell lysate at 20 µg

Lane 2:

HEK-293 (human embryonic kidney epithelial cell) whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution

Observed band size: 150 kDa

true

Exposure time: 180s

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)
  • WB

Lab

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)

This data was developed using ab307556, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

The antibody ab221154 exhibits low sensitivity in Western blot analyses. To improve detection of full-length TIE2, we recommend substituting with ab307556 or ab259982. Alternatively, experimental conditions can be optimized through increasing sample loading quantity, using lower antibody dilution or implementing femtogram-level sensitivity detection substrates.

Important note : TIE2 undergoes proteolytic cleavage (PMID : 32838837, PMID : 26666854). These three antibodies target distinct cleaved fragments of TIE2 due to differences in their immunogen localization.

Lane 1:

Western blot - Anti-TIE2 antibody [EPR21915] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr21915-ab221154'>ab221154</a>)

Lane 2:

Western blot - Anti-TIE2 antibody [EPR26540-78] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr26540-78-ab307556'>ab307556</a>)

Lane 3:

Western blot - Anti-TIE2 antibody [EPR23823-109] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr23823-109-ab259982'>ab259982</a>)

All lanes:

HUVEC (human umbilical vein endothelial cell line) whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 60 kDa,40 kDa,160 kDa

false

Exposure time: 40s

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)
  • WB

Supplier Data

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)

This data was developed using 307556, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST

TIE 2 is specifically expressed in endothelial cells and their progenitors (PMID : 8386827; PMID : 1630810; PMID : 8382358).

Low expression : mouse thymus (PMID : 8395828).

Lysates were freshly made and used for Western Blotting immediately to minimize protein degradation.

The identity of the bands lower than 75 kDa is unknown.

Exposure time :
Lanes 1-2 : 180 seconds
Lane 3 : 136 seconds

All lanes:

Western blot - Anti-TIE2 antibody [EPR26540-78] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr26540-78-ab307556'>ab307556</a>) at 1/1000 dilution

Lane 1:

Mouse lung tissue fresh lysate at 20 µg

Lane 2:

Mouse thymus tissue fresh lysate at 20 µg

Lane 3:

bEnd.3 (mouse brain endothelial cell) whole cell fresh lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 150 kDa

false

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)
  • WB

Lab

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)

This data was developed using ab307556, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

The antibody ab221154 exhibits low sensitivity in Western blot analyses. To improve detection of full-length TIE2 in mouse samples, we recommend substituting with ab307556. Alternatively, experimental conditions can be optimized through increasing sample loading quantity, using lower antibody dilution or implementing femtogram-level sensitivity detection substrates.

To preserve protein degradation, harvested cells were immediately lysed, followed by rapid gel electrophoresis and membrane transfer procedures.

Lanes 1 and 3:

Western blot - Anti-TIE2 antibody [EPR21915] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr21915-ab221154'>ab221154</a>) at 1/1000 dilution

Lanes 2 and 4:

Western blot - Anti-TIE2 antibody [EPR26540-78] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr26540-78-ab307556'>ab307556</a>) at 1/1000 dilution

Lanes 1 - 2:

bEnd.3 (mouse brain endothelial cell) fresh whole cell lysate at 20 µg

Lanes 3 - 4:

bEnd.3 (mouse brain endothelial cell) frozen whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 160 kDa

false

Exposure time: 180s

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)
  • WB

Lab

Western blot - Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free (AB307557)

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

The antibody ab221154 exhibits low sensitivity in Western blot analyses. To improve detection of full-length TIE2 in mouse samples, we recommend substituting with ab307556. Alternatively, experimental conditions can be optimized through increasing sample loading quantity, using lower antibody dilution or implementing femtogram-level sensitivity detection substrates.

This data was developed using ab307556, the same antibody clone in a different buffer formulation.

Lane 1:

Western blot - Anti-TIE2 antibody [EPR21915] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr21915-ab221154'>ab221154</a>) at 1/1000 dilution

Lane 2:

Western blot - Anti-TIE2 antibody [EPR26540-78] (<a href='/en-us/products/primary-antibodies/tie2-antibody-epr26540-78-ab307556'>ab307556</a>) at 1/1000 dilution

All lanes:

Mouse lung tissue lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution

Observed band size: 160 kDa

false

Exposure time: 180s

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR26540-78

Isotype

IgG

Carrier free

Yes

Reacts with

Human, Mouse

Applications

WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

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Product details

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.

Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.

Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

TIE2 also known as TEK or CD202B is a receptor tyrosine kinase with a mass of approximately 145 kDa. It plays an important role in vascular development and maintenance. TIE2 is mainly expressed in endothelial cells which line the interior surface of blood vessels. It binds angiopoietins predominantly Angiopoietin-1 (Angpt1) influencing vascular stability and permeability. Researchers use TIE2 antibodies including anti-TIE and anti-clone to study its role and functions across various contexts.
Biological function summary

TIE2 plays a central role in angiogenesis and blood vessel maturation. It forms a receptor complex with other components to mediate its effects. This interaction mainly involves Angpt1 which binds to TIE2 stabilizing blood vessels and preserving their integrity. TIE2 also participates in cell survival and migration processes necessary for normal vascular function. Researchers often perform Angpt1 ELISA in bulk to quantify interactions involving TIE2 in experiments.

Pathways

TIE2 is important in the angiopoietin-TIE signaling pathway regulating vascular development. TIE2 is related to proteins such as Angpt1 which are centrally involved in this pathway. It also interacts with various signaling molecules including phosphatidylinositol-3-kinase (PI3K) which contributes to cell survival pathways. Alterations in the TIE2 signaling cascade can lead to aberrant angiogenesis and related pathologies.

TIE2 is implicated in several vascular diseases and cancer. Mutations or dysregulation of TIE2 can result in venous malformations and further compromise blood vessel integrity. In cancer TIE2 expression can influence tumor angiogenesis enhancing tumor growth and metastasis. TIE2 interacts with proteins like vascular endothelial growth factor (VEGF) which are involved in neovascularization and cancer progression. Understanding these interactions helps target therapeutic strategies in relevant diseases.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Tyrosine-protein kinase that acts as a 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 pro-inflammatory plasma proteins and leukocytes from blood vessels. Required for normal angiogenesis and heart development during embryogenesis. Required for post-natal hematopoiesis. After birth, activates or inhibits angiogenesis, depending on the context. Inhibits angiogenesis and promotes vascular stability in quiescent vessels, where endothelial cells have tight contacts. In quiescent vessels, ANGPT1 oligomers recruit TEK to cell-cell contacts, forming complexes with TEK molecules from adjoining cells, and this leads to preferential activation of phosphatidylinositol 3-kinase and the AKT1 signaling cascades. In migrating endothelial cells that lack cell-cell adhesions, ANGT1 recruits TEK to contacts with the extracellular matrix, leading to the formation of focal adhesion complexes, activation of PTK2/FAK and of the downstream kinases MAPK1/ERK2 and MAPK3/ERK1, and ultimately to the stimulation of sprouting angiogenesis. ANGPT1 signaling triggers receptor dimerization and autophosphorylation at specific tyrosine residues that then serve as binding sites for scaffold proteins and effectors. Signaling is modulated by ANGPT2 that has lower affinity for TEK, can promote TEK autophosphorylation in the absence of ANGPT1, but inhibits ANGPT1-mediated signaling by competing for the same binding site. Signaling is also modulated by formation of heterodimers with TIE1, and by proteolytic processing that gives rise to a soluble TEK extracellular domain. The soluble extracellular domain modulates signaling by functioning as decoy receptor for angiopoietins. TEK phosphorylates DOK2, GRB7, GRB14, PIK3R1; SHC1 and TIE1.
See full target information TEK

Product promise

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