Anti-TIE2 antibody [EPR26540-78] - BSA and Azide free
- RabMAb
- Recombinant
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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
- 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
- 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
- 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
- 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
- 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
Related conjugates and formulations (1)
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Anti-TIE2 antibody [EPR26540-78]
Reactivity data
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
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
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.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com