Anti-TRPA1/TSA antibody [EPR26211-139] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal TRPA1/TSA antibody. Carrier free. Suitable for IHC-P, WB and reacts with Transfected cell line - Human, Human samples.
View Alternative Names
ANKTM1, TRPA1, Transient receptor potential cation channel subfamily A member 1, Ankyrin-like with transmembrane domains protein 1, Transformation-sensitive protein p120, Wasabi receptor, p120
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPA1/TSA antibody [EPR26211-139] - BSA and Azide free (AB320716)
This data was developed using ab320715, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded (A) HEK-293T (human epithelial cell line from embryonic kidney) transfected with a TRPA1 expression vector containing a Myc-His tag. (B) HEK-293T transfected with empty vector containing a Myc-His tag. tissue labeling TRPA1/TSA with ab320715 at 1/2000 (0.25 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on (A) HEK-293T (human epithelial cell line from embryonic kidney) transfected with a TRPA1 expression vector containing a Myc-His tag, negative staining on (B) HEK-293T transfected with empty vector containing a Myc-His tag. The section was incubated with ab320715 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPA1/TSA antibody [EPR26211-139] - BSA and Azide free (AB320716)
This data was developed using ab320715, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling TRPA1/TSA with ab320715 at 1/50 (9.98 ug/ml) dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Negative control : no staining on human liver. The section was incubated with ab320715 at 4°C overnight. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPA1/TSA antibody [EPR26211-139] - BSA and Azide free (AB320716)
This data was developed using ab320715, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human lung tissue labeling TRPA1/TSA with ab320715 at 1/50 (9.98 ug/ml) dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Negative control : no staining on human lung. The section was incubated with ab320715 at 4°C overnight. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPA1/TSA antibody [EPR26211-139] - BSA and Azide free (AB320716)
This data was developed using ab320715, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human dorsal root ganglion (DRG) tissue labeling TRPA1/TSA with ab320715 at 1/50 (9.98 ug/ml) dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Positive staining on human dorsal root ganglion (DRG). The section was incubated with ab320715 at 4°C overnight. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPA1/TSA antibody [EPR26211-139] - BSA and Azide free (AB320716)
This data was developed using ab320715, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Muscularis of human colon tissue labeling TRPA1/TSA with ab320715 at 1/50 (9.98 ug/ml) dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Positive staining on myenteric ganglia of human colon (PMID : 28478727). The section was incubated with ab320715 at 4°C overnight. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer) (ab214880). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0)
- WB
Supplier Data
Western blot - Anti-TRPA1/TSA antibody [EPR26211-139] - BSA and Azide free (AB320716)
This data was developed using ab320715, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Low expression : HEK-293, T-47D, Jurkat. The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 24008932). The identity of the band higher than 250 kDa (in lanes 2-3) is unknown. The identity of the lower MW bands at approximately 15 kDa (in lane 4) and 45 kDa (in lane 5) are unknown. In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-TRPA1/TSA antibody [EPR26211-139] (<a href='/en-us/products/primary-antibodies/trpa1-tsa-antibody-epr26211-139-ab320715'>ab320715</a>) at 1/1000 dilution
Lane 1:
U-2 OS (human bone osteosarcoma epithelial cell) whole cell lysate at 50 µg
Lane 2:
MRC-5 (human lung fibroblast) whole cell lysate at 50 µg
Lane 3:
WI-8 (human fetal lung fibroblast) whole cell lysate at 50 µg
Lane 4:
HEK-293 (human embryonic kidney epithelial cell) whole cell lysate at 50 µg
Lane 5:
T-47D (human ductal breast epithelial tumor epithelial cell) whole cell lysate at 50 µg
Lane 6:
Jurkat (human T cell leukemia T lymphocyte from peripheral blood) whole cell lysate at 50 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: 130 kDa,140 kDa,36 kDa
false
Exposure time: 81s
Related conjugates and formulations (1)
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Anti-TRPA1/TSA antibody [EPR26211-139]
Reactivity data
Product details
ab320716 is the carrier-free version of ab320715.
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
TRPA1 contributes significantly to the sensation of pain and irritation. Functioning as a part of a receptor complex on the cellular membrane it integrates environmental stimuli to trigger responses such as pain and inflammation. TRPA1 interacts with various ligands which can modulate its activity leading to the perception of noxious cold and harsh chemical conditions. Recent studies also revealed its involvement in bronchial conditions implicating compounds like eucalyptol and related derivatives in modulating its effects.
Pathways
TRPA1 interacts with several critical sensory pathways involved in pain and thermosensation. It is an important player within the neurogenic inflammation pathway and the nociceptive pathway. In these pathways TRPA1 often acts together with related proteins like TRPV1 further modulating the response to heat and capsaicin. These interactions suggest a complex interplay between different TRP channels influencing how organisms react to different harmful stimuli.
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'.
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