Anti-CYP2C11 antibody
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(16 Publications)
Rabbit Polyclonal CYP2C11 antibody. Suitable for IHC-P, ICC/IF and reacts with Rat, Human samples. Cited in 16 publications. Immunogen corresponding to Synthetic Peptide within Rat Cyp2c11 aa 1-100.
View Alternative Names
Cyp2c, Cyp2c-11, Cyp2c11, Cytochrome P450 2C11, CYPIIC11, Cytochrome P-450(M-1), Cytochrome P450-UT-2, Cytochrome P450-UT-A, Cytochrome P450H
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CYP2C11 antibody (AB3571)
ab3571 staining CYP2C11 (green) in HeLa (Human epithelial adenocarcinoma cell line) cells (right), compared to control (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with primary antibody (1 : 100 in 3% BSA-PBS) overnight at 4 °C. A DyLight-conjugated anti-rabbit was used as the secondary antibody. Red (phalloidin) - F-actin, Blue - nuclei. Images were taken at a magnification of 60x.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CYP2C11 antibody (AB3571)
IHC image of ab3571 staining in human renal carcinoma formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab3571, 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CYP2C11 antibody (AB3571)
ab3571 staining CYP2C11 (green) in PC-12 (Rat adrenal gland pheochromocytoma cell line) cells (right), compared to control (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with primary antibody (1 : 100 in 3% BSA-PBS) overnight at 4 °C. A DyLight-conjugated anti-rabbit was used as the secondary antibody. Red (phalloidin) - F-actin, Blue - nuclei. Images were taken at a magnification of 60x.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CYP2C11 antibody (AB3571)
ab3571 staining CYP2C11 (green) in H-4-II-E (Rat hepatoma cell line) cells (right), compared to control (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with primary antibody (1 : 100 in 3% BSA-PBS) overnight at 4 °C. A DyLight-conjugated anti-rabbit was used as the secondary antibody. Red (phalloidin) - F-actin, Blue - nuclei. Images were taken at a magnification of 60x.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CYP2C11 antibody (AB3571)
ab3571 staining CYP2C11 in the cytoplasm of rat liver tissue (right) compared with a negative control in the absence of primary antibody (left) by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). To expose target proteins, antigen retrieval method was performed using 10mM sodium citrate (pH 6.0) microwaved for 8-15 min. Tissues were then blocked in 3% H2O2-methanol for 15 min at room temperature. Sections were incubated with primary antibody (1 : 200 in 3% BSA-PBS) overnight at 4°C. A HRP-conjugated anti-rabbit was used as the secondary antibody, followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CYP2C11 antibody (AB3571)
ab3571 staining CYP2C11 in the cytoplasm of rat kidney tissue (right) compared with a negative control in the absence of primary antibody (left) by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). To expose target proteins, antigen retrieval method was performed using 10mM sodium citrate (pH 6.0) microwaved for 8-15 min. Tissues were then blocked in 3% H2O2-methanol for 15 min at room temperature. Sections were incubated with primary antibody (1 : 200 in 3% BSA-PBS) overnight at 4°C. A HRP-conjugated anti-rabbit was used as the secondary antibody, followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.
Reactivity data
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Supplementary information
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Biological function summary
Cytochrome P450 2C11 participates in the metabolism of steroids through oxidative reactions. It plays a role in converting testosterone into its hydroxylated metabolites which are important for maintaining homeostasis. CYP2C11 often acts independently but can also be associated with other proteins that facilitate the electron transfer needed for oxygenation reactions. Its activity can be influenced by factors like hormonal changes and stress.
Pathways
CYP2C11 contributes significantly to the lipid metabolism pathway and drug metabolism pathway. It has functional relevance in transforming chemicals that are either taken up by the body or produced within it. The enzyme CYP3A1 shares a functional relationship with CYP2C11 in these pathways broadening the spectrum of compounds processed. The modulation of CYP2C11 affects the concentrations of various metabolites impacting systemic homeostasis.
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Target data
Publications (16)
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Chemical & pharmaceutical bulletin 71:334-341 PubMed36858593
2023
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Frontiers in pharmacology 12:622040 PubMed33967756
2021
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Biological & pharmaceutical bulletin 44:96-102 PubMed33390555
2021
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Pharmaceutics 12: PubMed33238436
2020
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British journal of pharmacology 178:582-599 PubMed33119943
2020
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International journal of biological sciences 15:2037-2050 PubMed31592228
2019
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Molecular medicine reports 20:771-778 PubMed31180561
2019
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Journal of ethnopharmacology 235:100-110 PubMed30710735
2019
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Drug metabolism and disposition: the biological fa 45:1336-1344 PubMed28935656
2017
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Laboratory investigation; a journal of technical m 97:782-791 PubMed28319086
2017
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