Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70]
- 20ul selling size
- RabMAb
- Recombinant
- KO Validated
- What is this?
Be the first to review this product! Submit a review
|
(1 Publication)
Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] is a Rabbit Monoclonal antibody that is used in Aryl hydrocarbon Receptor Flow Cytometry (Intra), Western Blot. Suitable for Mouse samples.
The Aryl Hydrocarbon Receptor (AhR) is a ligand-activated transcription factor. It is involved in various processes such as tumor initiation, progression, and metastasis. Studies on various tumor types and tumor cell lines have shown high AhR expression, suggesting that AhR is activated constitutively in tumors and facilitates their growth. AhR affects the immune system's ability to target cancer cells. For example, inhibiting AhR can restore normal NK cell maturation and enhance their ability to kill cancer cells.
View Alternative Names
Aryl hydrocarbon receptor, Ah receptor, AhR, Ahr
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (AB309491)
Immunohistochemical analysis of formalin fixed paraffin embedded mice liver labelling Aryl hydrocarbon Receptor with ab309491 at a concentration of 1/200 dilution. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The primary antibody Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] was incubated for 30 mins at room temperature. Sections were counterstained with Hematoxylin. Positive staining on mouse liver.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (AB309491)
Immunohistochemical analysis of formalin fixed paraffin embedded mice breast carcinoma labelling Aryl hydrocarbon Receptor with ab309491 at a concentration of 1/200 dilution. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The primary antibody Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] was incubated for 30 mins at room temperature. Sections were counterstained with Hematoxylin. Positive staining on mouse breast carcinoma.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (AB309491)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Neuro-2a (mouse neuroblastoma neuroblast, Left) / HEPA1-6 (mouse hepatoma epithelial cell, Right) cells labelling Aryl hydrocarbon Receptor with ab309491 at 1/500 dilution (0.1 ug)/Right (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody. Negative control : Neuro-2a(PMID : 16956419).
- WB
Lab
Western blot - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (AB309491)
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Ahr-KO homozygous mice (Strain ID : T012419).
All lanes:
Western blot - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (ab309491) at 1/1000 dilution
Lane 1:
Wild-type mouse lung tissue lysate (male) at 20 µg
Lane 2:
Ahr knockout mouse lung tissue lysate (male case1) at 20 µg
Lane 3:
Ahr knockout mouse lung tissue lysate (male case2) 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: 100 kDa,36 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (AB309491)
Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : Neuro-2a(PMID : 16956419) Lysates were freshly made and used for Western blotting immediately to minimize protein degradation. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (ab309491) at 1/1000 dilution
Lane 1:
C2C12 (mouse myoblast) whole cell lysate at 20 µg
Lane 2:
Hepa1-6 (mouse hepatoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 100 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (AB309491)
Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : Pancreas In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (ab309491) at 1/1000 dilution
Lane 1:
Mouse lung tissue lysate at 20 µg
Lane 2:
Mouse pancreas 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 1/100000 dilution
Observed band size: 100 kDa
false
Exposure time: 180s
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] (AB309491)
Immunohistochemical analysis of formalin fixed paraffin embedded mice lung tissue labelling Aryl hydrocarbon Receptor with ab309491 at a concentration of 1/200 dilution. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The primary antibody Anti-Aryl hydrocarbon Receptor antibody [EPR27537-70] was incubated for 30 mins at room temperature. Sections were counterstained with Hematoxylin. Positive staining on (A) Lung tissue from wild-type C57BL/6J mice, no staining on (B) Lung tissue from Ahr knockout mice. The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Ahr-KO homozygous mice (Strain ID : T012419).
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The AhR plays an important role in the regulation of detoxification enzymes such as cytochrome P450s. This receptor functions as a sensor for environmental toxins activating detoxification pathways once bound to ligands. It also contributes to the modulation of immune responses and development processes. The AhR often forms part of a larger protein complex to exert its effects on gene expression and cellular processes.
Pathways
The AhR significantly participates in the xenobiotic metabolism pathway and the dioxin signaling pathway. It interacts with proteins such as ARNT and cytochrome P450 enzymes to mediate the cellular response to toxins. The activity of AhR regulates the expression of phase I and phase II detoxification enzymes making it an integral part of the body’s defense against environmental chemicals.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Heliyon 10:e32260 PubMed38882349
2024
Applications
Unspecified application
Species
Unspecified reactive species
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