Anti-Cytochrome P450 1A2 antibody [EPR28416-31]
- BOND RX™ Validated
- 20ul selling size
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal Cytochrome P450 1A2 antibody. Suitable for IHC-P, WB, IP and reacts with Mouse, Rat, Transfected cell lysate - Mouse samples. Cited in 1 publication.
View Alternative Names
Cyp1a-2, Cyp1a2, Cytochrome P450 1A2, CYPIA2, Cholesterol 25-hydroxylase, Cytochrome P450-P2, Cytochrome P450-P3, Hydroperoxy icosatetraenoate dehydratase
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Immunohistochemical analysis of paraffin-embedded Mouse colon tissue labeling Cytochrome P450 1A2 with ab314666 at 1/2000 (0.256 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on mouse colon (PMID : 31147315). The section was incubated with ab314666 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-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling Cytochrome P450 1A2 with ab314666 at 1/2000 (0.256 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on mouse cerebrum (PMID : 31147315). The section was incubated with ab314666 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-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Immunohistochemical analysis of paraffin-embedded Rat colon tissue labeling Cytochrome P450 1A2 with ab314666 at 1/2000 (0.256 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on rat colon. The section was incubated with ab314666 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-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling Cytochrome P450 1A2 with ab314666 at 1/2000 (0.256 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on rat cerebrum. The section was incubated with ab314666 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-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Immunohistochemical analysis of paraffin-embedded rat liver tissue labeling Cytochrome P450 1A2 with ab314666 at 1/2000 (0.256 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Rat liver showed expected staining patterns (PMID : 36220068, PMID : 34873187). The section was incubated with ab314666 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-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Immunohistochemical analysis of paraffin-embedded mouse liver tissue labeling Cytochrome P450 1A2 with ab314666 at 1/2000 (0.256 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Mouse liver showed expected staining patterns (PMID : 36220068, PMID : 34873187)). The section was incubated with ab314666 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.
- IP
Supplier Data
Immunoprecipitation - Anti-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Cytochrome P450 1A2 was immunoprecipitated from 0.35 mg Mouse liver tissue lysate with ab314666 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab314666 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : Mouse liver tissue lysate Lane 2 : ab314666 IP in Mouse liver tissue lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab314666 in mouse liver tissue lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-Cytochrome P450 1A2 antibody [EPR28416-31] (ab314666) at 1/30 dilution
All lanes:
Mouse liver tissue lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 41s
- WB
Supplier Data
Western blot - Anti-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : colon, brain, testis, spleen. In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Cytochrome P450 1A2 antibody [EPR28416-31] (ab314666) at 1/1000 dilution
Lane 1:
Mouse liver tissue lysate at 20 µg
Lane 2:
Mouse colon tissue lysate at 20 µg
Lane 3:
Mouse brain tissue lysate at 20 µg
Lane 4:
Mouse testis tissue lysate at 20 µg
Lane 5:
Mouse spleen 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: 55 kDa
false
Exposure time: 59s
- WB
Supplier Data
Western blot - Anti-Cytochrome P450 1A2 antibody [EPR28416-31] (AB314666)
Blocking and diluting buffer and concentration : 5% NFDM/TBST This antibody does not cross-react with mouse CP1A1. In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution. In Western blot, Anti-6X His tag antibody [EPR20547]-CHIP Grade (ab213204) staining at 1/5000 dilution.
All lanes:
Western blot - Anti-Cytochrome P450 1A2 antibody [EPR28416-31] (ab314666) at 1/1000 dilution
Lane 1:
293T cells transfected with an empty vector containing a His-tag, whole cell lysate at 20 µg
Lane 2:
293T cells transfected with a mouse CP1A1 expression vector containing a His-tag, whole cell lysate at 20 µg
Lane 3:
293T cells transfected with a mouse CP1A2 expression vector containing a His-tag, whole cell 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: 55 kDa
false
Exposure time: 92s
Related conjugates and formulations (1)
-
Anti-Cytochrome P450 1A2 antibody [EPR28416-31] - BSA and Azide free
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
CYP1A2 plays a central role in the oxidative biotransformation of drugs and procarcinogens. It does not form part of a larger complex but interacts dynamically with other enzymes in the detoxification process. CYP1A2 metabolizes several clinical drugs such as caffeine and theophylline and regulates the detoxification of aromatic amines and hydrocarbons. Studying CYP1A2 inhibitors can provide insights into clinically relevant drug interactions and potential side effects in pharmacotherapy.
Pathways
CYP1A2 functions within the drug metabolism and synthesis of cholesterol steroids and other lipids pathways. In the drug metabolism pathway CYP1A2 works alongside other cytochrome P450 enzymes such as CYP1A1 and CYP1B1 which together ensure the metabolism and clearance of various exogenous and endogenous compounds. These pathways are vital for maintaining drug efficacy and preventing toxicity through the metabolic clearance of pharmaceutical agents and harmful substances.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Materials today. Bio 32:101700 PubMed40225139
2025
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'.
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