Mouse Monoclonal antibody. Suitable for WB, Dot, ICC/IF and reacts with Synthetic peptide samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
IP | WB | Dot | ICC/IF | |
---|---|---|---|---|
Synthetic peptide | Not recommended | Tested | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide | Dilution info 1/100 | Notes - |
Mouse Monoclonal antibody. Suitable for WB, Dot, ICC/IF and reacts with Synthetic peptide samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
The T2A and P2A sequences commonly referred to as 2A peptides function as self-cleaving peptides that facilitate the expression of multiple proteins from a single gene construct. These peptides act as short sequences of amino acids that cause ribosomal skipping during translation resulting in discrete protein products. T2A and P2A are used as linker sequences and their use is often interchangeable in molecular biology techniques for polycistronic expression systems. The T2A peptide is derived from the Thosea asigna virus while P2A originates from the Porcine teschovirus-1. These sequences are small with a mass typically around 2 kDa and they are primarily expressed where polycistronic vectors are utilized such as in transgenic organisms or recombinant protein production systems.
T2A and P2A peptides play a significant role in the facilitation of protein co-expression in a variety of organisms. They do not form part of any multi-protein complex but enable independent expression of protein components from within a single vector by cleaving themselves during protein translation. This ability is especially beneficial for engineering purposes where researchers require stable gene expression and production of multiple proteins simultaneously without the complication of internal ribosomal entry sites (IRES) or additional subunits.
T2A and P2A peptides do not directly belong to classical biological pathways as they do not exist as conventional proteins. Instead they influence pathways facilitated by the proteins they help express. These peptides are employed in reverse engineering cellular pathways where simultaneous gene expression is desired such as the Wnt signaling pathway or apoptosis regulation. Both pathways involve key proteins that can be expressed using T2A and P2A sequences allowing researchers to construct and study artificial biological systems with enhanced control.
T2A and P2A peptides find significance in the study and therapeutic targeting of conditions like cancer and neurodegenerative diseases. In cancer research for instance these peptides enable the co-expression of oncogenes and tumor suppressors helping to elucidate their roles in tumorigenesis. Neurodegenerative disorders such as Parkinson's disease also benefit from their application as T2A and P2A sequences allow for the expression of multiple therapeutic proteins including growth factors like GDNF offering insights into potential combinatorial treatments. By facilitating multi-gene expression these peptides are integral to advancing understanding and therapeutic developments in complex diseases.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
All lanes: Western blot - Anti-T2A + P2A antibody [3H4] (ab269488) at 1/1000 dilution
Lane 1: 293T( human embryonic kidney epithelial cell) transfected with an empty vector (vector control), containing a GFP tag and myc-His-tag®, whole cell lysate at 10 µg
Lane 2: 293T transfected with T2A expression vector containing a GFP tag and myc-His-tag®, whole cell lysate at 10 µg
Lane 3: 293T transfected with P2A expression vector containing a GFP tag and myc-His-tag®, whole cell lysate at 10 µg
Lane 4: HeLa (human epithelial cell line from cervix adenocarcinoma), whole cell lysate at 10 µg
Lane 5: NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 10 µg
Lane 6: C6 (rat glial tumor glial cell), whole cell lysate at 10 µg
All lanes: Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/5000 dilution
Exposure time: 10s
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized 293T cells labelling T2A + P2A with ab269488 at 1/100 (9.29 ug/ml) dilution, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119 Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed (Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119) antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing cytoplasmic and nuclear staining in HEK-293T cells transfected with a T2A expression vector containing a GFP tag is observed. The Nuclear counterstain was DAPI (Blue). Secondary antibody only control: Secondary antibody is Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119 Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed (Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119) at 1/1000 2 ug/ml dilution.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized 293T cells labelling T2A + P2A with ab269488 at 1/100 (9.29 ug/ml) dilution, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119 Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed (Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119) antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing cytoplasmic and nuclear staining in HEK-293T cells transfected with a P2A expression vector containing a GFP tag is observed. The Nuclear counterstain was DAPI (Blue). Secondary antibody only control: Secondary antibody is Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119 Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed (Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119) at 1/1000 2 ug/ml dilution.
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