![Western Blot: TRPA1 Antibody [NB100-91319] - Tissue lysates. Blocking: 1% LFDM for 30 min at RT; primary antibody: dilution 1:6000 incubated overnight at 4C.](http://images.novusbio.com/fullsize/TRPA1-Antibody-Western-Blot-NB100-91319-img0001.jpg "Western Blot: TRPA1 Antibody [NB100-91319] - Tissue lysates. Blocking: 1% LFDM for 30 min at RT; primary antibody: dilution 1:6000 incubated overnight at 4C.")
| Reactivity | Hu, Mu, Rt, PmSpecies Glossary |
| Applications | WB, ICC/IF, IHC |
| Clonality | Polyclonal |
| Host | Rabbit |
| Conjugate | Unconjugated |
| Concentration | LYOPH |
| Immunogen | A synthetic peptide from rat TRPA1 conjugated to blue carrier protein was used as the antigen. The peptide is homologous in mouse. |
| Isotype | IgG |
| Clonality | Polyclonal |
| Host | Rabbit |
| Gene | TRPA1 |
| Purity | Unpurified |
| Innovator's Reward | Test in a species/application not listed above to receive a full credit towards a future purchase. |
| Dilutions |
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| Application Notes | Use in Immunocytochemistry/immunofluorescence reported in scientific literature (PMID: 30707612). |
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| Theoretical MW | 128 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
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| Publications |
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| Storage | Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles. |
| Buffer | Lyophilized from whole antisera |
| Preservative | No Preservative |
| Concentration | LYOPH |
| Purity | Unpurified |
| Reconstitution Instructions | Reconstitute in 0.1 ml of sterile water. Centrifuge to remove any insoluble material. Glycerol may be added (1:1) for additional stability. Please note the sample size is provided in reconstituted format. |
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Secondary Antibodies |
Isotype Controls |
Research Areas for TRPA1 Antibody (NB100-91319)Find related products by research area.
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Winter is coming, and TRPM8 welcomes the cold! TRPM8, or transient receptor potential melastatin 8, is a nonselective cation channel that is activated by cold environments and menthol-like cooling compounds. While TRPM8 is best known for its location in peripheral nerve endings, it has functio... Read full blog post. |
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TRPA1: A contributor to itching and inflammation? Scratch that! Transient receptor potential A1 (TRPA1) is an ion channel found on the plasma membrane of many cell types that functions in diverse sensory processes such as pain and temperature. The TRPA1 ion channel is specifically expressed in nociceptive neurons,... Read full blog post. |
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Touch Infographic: From Touch Receptors to the Brain The body contains thousands of receptors and nerves which allow us to experience the sense of touch, also referred to as tactile perception. The somatosensory system allows organisms to perceive and decode a wide range of tactile stimuli to allow for ... Read full blog post. |
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![Western Blot: TRPA1 Antibody [NB100-91319] - TRPA1 inhibitor HC030031 significantly ameliorated the oxidative stress & apoptosis levels of Pg.LPS-induced PDLCs. (a) P.g.LPS increased intracellular calcium ion level in a dose-dependent manner (n = 3). (b) Lower HC030031 concentration significantly reversed the increase of intracellular calcium ions, & 10 μM HC030031 was used in the subsequent experiment (n = 3). (c) Flow cytometry analysis of the control group (PDLCs only, C), L group (PDLCs treated by LPS, L), & LH group (PDLCs treated by 10 μM HC030031 & LPS, LH) (n = 4). (d, e) Western blot analysis & semiquantitative statistical analysis of oxidative stress, apoptosis, & TRPA1 proteins in in C, L, & LH groups (n = 3). (f) EM images showing endoplasmic reticulum (yellow arrows) & mitochondrial morphology (red arrows) of PDLCs in Ctr, LPS, & LH groups (white stars represent cell nuclei) (n = 4). (g) Quantification of endoplasmic reticulum size, mitochondrial size, mitochondrial number per cell (n = 4), & mitochondrial crista density was analyzed (>100 mitochondria). Data analysis was performed by using one-way ANOVA (∗P < 0.05, ∗∗P < 0.01, & ∗∗∗P < 0.001). Data are presented as the mean ± SEM. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/35720191), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb100-91319_rabbit-polyclonal-trpa1-antibody-31020241628499.jpg "Western Blot: TRPA1 Antibody [NB100-91319] - TRPA1 inhibitor HC030031 significantly ameliorated the oxidative stress & apoptosis levels of Pg.LPS-induced PDLCs. (a) P.g.LPS increased intracellular calcium ion level in a dose-dependent manner (n = 3). (b) Lower HC030031 concentration significantly reversed the increase of intracellular calcium ions, & 10 μM HC030031 was used in the subsequent experiment (n = 3). (c) Flow cytometry analysis of the control group (PDLCs only, C), L group (PDLCs treated by LPS, L), & LH group (PDLCs treated by 10 μM HC030031 & LPS, LH) (n = 4). (d, e) Western blot analysis & semiquantitative statistical analysis of oxidative stress, apoptosis, & TRPA1 proteins in in C, L, & LH groups (n = 3). (f) EM images showing endoplasmic reticulum (yellow arrows) & mitochondrial morphology (red arrows) of PDLCs in Ctr, LPS, & LH groups (white stars represent cell nuclei) (n = 4). (g) Quantification of endoplasmic reticulum size, mitochondrial size, mitochondrial number per cell (n = 4), & mitochondrial crista density was analyzed (>100 mitochondria). Data analysis was performed by using one-way ANOVA (∗P < 0.05, ∗∗P < 0.01, & ∗∗∗P < 0.001). Data are presented as the mean ± SEM. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/35720191), licensed under a CC-BY license. Not internally tested by Novus Biologicals.")
![Western Blot: TRPA1 Antibody [NB100-91319] - Periodontitis-derived periodontal ligament cells & tissues were at high levels of oxidative stress & apoptosis. (a) The related gene expressions of oxidative stress, apoptosis, & some of the TRP families in healthy & periodontitis-derived periodontal ligament cells (PDLCs & P-PDLCs) (n = 3). (b, c) Western blot & semiquantitative statistical analysis of oxidative stress, apoptosis, & TRPA1 in PDLCs & P-PDLCs. (n = 3). d, Flow cytometry analysis of PDLCs & P-PDLCs (n = 4). (e, f) H&E staining (white star represent immune cell infiltration), immunohistochemistry & immunofluorescence staining, & semiquantitative statistical analysis of periodontitis & healthy derived periodontal ligament tissues (PDLTs & P-PDLTs) (n = 3). Data analysis was performed by using Student's t-test (∗P < 0.05, ∗∗P < 0.01, & ∗∗∗P < 0.001). The data are presented as the mean ± SEM. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/35720191), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb100-91319_rabbit-polyclonal-trpa1-antibody-310202416284922.jpg "Western Blot: TRPA1 Antibody [NB100-91319] - Periodontitis-derived periodontal ligament cells & tissues were at high levels of oxidative stress & apoptosis. (a) The related gene expressions of oxidative stress, apoptosis, & some of the TRP families in healthy & periodontitis-derived periodontal ligament cells (PDLCs & P-PDLCs) (n = 3). (b, c) Western blot & semiquantitative statistical analysis of oxidative stress, apoptosis, & TRPA1 in PDLCs & P-PDLCs. (n = 3). d, Flow cytometry analysis of PDLCs & P-PDLCs (n = 4). (e, f) H&E staining (white star represent immune cell infiltration), immunohistochemistry & immunofluorescence staining, & semiquantitative statistical analysis of periodontitis & healthy derived periodontal ligament tissues (PDLTs & P-PDLTs) (n = 3). Data analysis was performed by using Student's t-test (∗P < 0.05, ∗∗P < 0.01, & ∗∗∗P < 0.001). The data are presented as the mean ± SEM. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/35720191), licensed under a CC-BY license. Not internally tested by Novus Biologicals.")
![Western Blot: Goat anti-Rabbit IgG (H+L) Secondary Antibody [HRP] [NB7160] - Western blot showing vemurafenib treatment in BRAFV600E CRC cells inhibits fission mediator DRP1 with no significant effect on fusion proteins (Mfn1 & 2) using MFN-1 antibody (NBP1-51841) and corresponding secondary antibody, goat anti-rabbit IgG-HRP (NB7160). Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33738242).](https://images.novusbio.com/images/Goat-anti-Rabbit-IgG-H+L-Secondary-Antibody-HRP-Western-Blot-NB7160-img0001.jpg "Western Blot: Goat anti-Rabbit IgG (H+L) Secondary Antibody [HRP] [NB7160] - Western blot showing vemurafenib treatment in BRAFV600E CRC cells inhibits fission mediator DRP1 with no significant effect on fusion proteins (Mfn1 & 2) using MFN-1 antibody (NBP1-51841) and corresponding secondary antibody, goat anti-rabbit IgG-HRP (NB7160). Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33738242).")
![Flow Cytometry: Rabbit IgG Isotype Control [NBP2-24891] - Intracellular FACS analysis of mouse TLR6 polyclonal antibody (red), rabbit isotype control (green), RAW cells alone (shaded). Two micrograms of antibodies were used. Goat anti-rabbit FITC (Novus, 20302) was used as secondary.](https://images.novusbio.com/images/Rabbit--Mouse-IgG-Isotype-Control-Flow-Cytometry-NBP2-24891-img0001.jpg "Flow Cytometry: Rabbit IgG Isotype Control [NBP2-24891] - Intracellular FACS analysis of mouse TLR6 polyclonal antibody (red), rabbit isotype control (green), RAW cells alone (shaded). Two micrograms of antibodies were used. Goat anti-rabbit FITC (Novus, 20302) was used as secondary.")