Anti-TRPV1 抗体 [EPR25057-67] - BSA and Azide free
Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal TRPV1 antibody. Carrier free. Suitable for WB, IHC-P, IHC-Fr, IP, ICC/IF and reacts with Human, Rat, Mouse samples.
別名を表示する
VR1, TRPV1, Transient receptor potential cation channel subfamily V member 1, TrpV1, Capsaicin receptor, Osm-9-like TRP channel 1, Vanilloid receptor 1, OTRPC1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
This data was developed using ab305299, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde fixed mouse DRG primary neurons permeabilized using 0.1% Triton X-100 labelling TRPV1 with ab305299 (green) followed by ab150081 AlexaFluor®488 preadsorbed Goat anti-Rabbit secondary. ab78078 anti-beta III Tubulin (mouse mAb) was used as counterstain (magenta) with ab150120 AlexaFluor®594 Goat anti-Mouse as secondary. Nuclear DNA was labelled with DAPI (shown in blue). Image showing cytoplasmic staining in mouse DRG primary neurons was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
This data was developed using ab305299, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde fixed rat DRG primary neurons permeabilized using 0.1% Triton X-100 labelling TRPV1 with ab305299 (green) followed by ab150081 AlexaFluor®488 preadsorbed Goat anti-Rabbit secondary. ab78078 anti-beta III Tubulin (mouse mAb) was used as counterstain (magenta) with ab150120 AlexaFluor®594 Goat anti-Mouse as secondary. Nuclear DNA was labelled with DAPI (shown in blue). Image showing cytoplasmic staining in rat DRG primary neurons was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IP
Supplier Data
Immunoprecipitation - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
This data was developed using ab305299, the same antibody clone in a different buffer formulation.
TRPV1 was immunoprecipitated from 0.35 mg Rat dorsal ganglion tissue lysate 10 μg with ab305299 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab305299. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Rat dorsal ganglion tissue lysate 10 μg
Lane 2 : ab305299 at 1/30 IP in Rat dorsal ganglion tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab305299 in Rat dorsal ganglion tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST
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:
Immunoprecipitation - Anti-TRPV1 antibody [EPR25057-67] (<a href='/products/primary-antibodies/trpv1-antibody-epr25057-67-ab305299'>ab305299</a>) at 1/1000 dilution
Lane 1:
Rat dorsal ganglion tissue at 10 µg
Lane 2:
<a href='/products/primary-antibodies/trpv1-antibody-epr25057-67-ab305299'>ab305299</a> at 1/30 IP in rat dorsal ganglion tissue lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 95 kDa
true
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
This data was developed using ab305299, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST The molecular weight is consistent to what has been described in literature (PMID : 25395667) Negative control : brain, cerebellum (PMID : 11243859) Samples are non-boiled as boiling may cause protein aggregation. Exposure time : 114 seconds
All lanes:
Western blot - Anti-TRPV1 antibody [EPR25057-67] (<a href='/products/primary-antibodies/trpv1-antibody-epr25057-67-ab305299'>ab305299</a>) at 1/1000 dilution
Lane 1:
Rat dorsal galion tissue lysate at 20 µg
Lane 2:
Rat brain tissue lysate at 40 µg
Lane 3:
Human spinal cord at 20 µg
Lane 4:
Human cerebellum at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 95 kDa
false
Exposure time: 114s
- WB
Lab
Western blot - Anti-TRPV1 antibody [EPR25057-67] - BSA and Azide free (AB305300)
This data was developed using ab305299, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
For Lane1, to minimize protein degradation, cell was lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
Samples are non-boiled as boiling may cause protein aggregation.
All lanes:
Western blot - Anti-TRPV1 antibody [EPR25057-67] (<a href='/products/primary-antibodies/trpv1-antibody-epr25057-67-ab305299'>ab305299</a>) at 1/1000 dilution
Lane 1:
Rat fresh dorsal ganglion tissue lysate at 40 µg
Lane 2:
Rat dorsal ganglion tissue lysate at 40 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 75 kDa,95 kDa
false
Exposure time: 180s
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Alexa Fluor® 647 Anti-TRPV1 antibody [EPR25057-67]
Reactivity data
製品の詳細
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.
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.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存温度
長期保存温度
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The role of TRPV1 extends beyond sensory perception. It is involved in detecting and regulating body temperature and is activated by heat acidic conditions and certain lipid metabolites. The receptor operates as part of a homotetrameric complex contributing to neural signaling. It is activated by chemical ligands such as capsaicin the compound responsible for the spicy sensation in chili peppers influencing pain and inflammation pathways.
Pathways
TRPV1 plays essential roles in pain and nociception pathways. It intersects with the inflammatory pathway where its activity is modulated by protein kinase C (PKC) and phospholipase C (PLC). These pathways involve calcium signaling and relate to proteins such as PKA and calcineurin which modulate TRPV1 activity through phosphorylation and dephosphorylation affecting the body's response to noxious stimuli.
製品プロトコール
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ターゲットの情報
Abcam product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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