Anti-AKR1C1/AKR1C2 antibody [EPR11542] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal AKR1C1 antibody. Carrier free. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Recombinant full length protein - Human samples. Cited in 1 publication.
View Alternative Names
DDH, DDH1, AKR1C1, Aldo-keto reductase family 1 member C1, 20alpha-hydroxysteroid dehydrogenase, 3beta-hydroxysteroid 3-dehydrogenase, Chlordecone reductase homolog HAKRC, Dihydrodiol dehydrogenase 1, High-affinity hepatic bile acid-binding protein, 20-alpha-HSD, DD1, HBAB
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-AKR1C1/AKR1C2 antibody [EPR11542] - BSA and Azide free (AB250092)
This data was developed using ab179448, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of permeabilized U87-MG cells labeling AKR1C1/AKR1C2 with ab179448 at 1/10 dilution (red), compared to a rabbit IgG negative control (green).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-AKR1C1/AKR1C2 antibody [EPR11542] - BSA and Azide free (AB250092)
Immunocytochemical/immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized U-87 MG (human glioblastoma- astrocytoma epithelial cell) cells labelling AKR1C1/AKR1C2 with primary antibody anti-AKR1C1/AKR1C2 (ab179448) at 1/500 dilution, followed by AlexaFluor®488 Goat anti-Rabbit (ab150077) secondary antibody at 1/1000 dilution. Confocal image showing cytoplasmic and nuclear staining in U-87 MG cell line. Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) was used to counterstain tubulin at 1 : 200 dilution. The nuclear counter stain is DAPI (blue).
This data was developed using ab179448, the same antibody clone in a different buffer formulation.
- IP
Supplier Data
Immunoprecipitation - Anti-AKR1C1/AKR1C2 antibody [EPR11542] - BSA and Azide free (AB250092)
AKR1C1/AKR1C2 was immunoprecipitated from U-87 MG lysates with ab179448 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab179448 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP) (ab131366) was used at 1/5000 dilution. Lane 1 : U-87 MG (human glioblastoma-astrocytoma epithelial cell) whole cell lysate 10 μg Lane 2 : ab179448 in U-87 MG (human glioblastoma-astrocytoma epithelial cell) whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab179448 in U-87 MG whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-AKR1C1/AKR1C2 antibody [EPR11542] (<a href='/en-us/products/primary-antibodies/akr1c1-akr1c2-antibody-epr11542-ab179448'>ab179448</a>) at 1/30 dilution
All lanes:
U-87 MG lysates
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: 180s
- WB
Supplier Data
Western blot - Anti-AKR1C1/AKR1C2 antibody [EPR11542] - BSA and Azide free (AB250092)
Blocking buffer and concentration : 5% NFDM/TBST. Diluting buffer and concentration : 5% NFDM/TBST. This data was developed using ab179448, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-AKR1C1/AKR1C2 antibody [EPR11542] (<a href='/en-us/products/primary-antibodies/akr1c1-akr1c2-antibody-epr11542-ab179448'>ab179448</a>) at 1/1000 dilution
Lane 1:
His-tagged human AKR1C1 recombinant protein, full-length
Lane 2:
His-tagged human AKR1C2 recombinant protein, full-length
Lane 3:
His-tagged human AKR1C3 recombinant protein, full-length
Lane 4:
His-tagged human AKR1C4 recombinant protein, full-length
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 1/20000 dilution
Observed band size: 39 kDa
false
Exposure time: 40s
- WB
Supplier Data
Western blot - Anti-AKR1C1/AKR1C2 antibody [EPR11542] - BSA and Azide free (AB250092)
This data was developed using ab179448, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-AKR1C1/AKR1C2 antibody [EPR11542] (<a href='/en-us/products/primary-antibodies/akr1c1-akr1c2-antibody-epr11542-ab179448'>ab179448</a>) at 1/1000 dilution
Lane 1:
HepG2 lysate at 10 µg
Lane 2:
U87-MG lysate at 10 µg
Lane 3:
Human fetal liver lysate at 10 µg
Lane 4:
HeLa lysate at 10 µg
Predicted band size: 37 kDa
false
Related conjugates and formulations (1)
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Anti-AKR1C1/AKR1C2 antibody [EPR11542]
Reactivity data
Product details
ab250092 is the carrier-free version of ab179448.
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.
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The AKR1C1/AKR1C2 enzymes play significant roles in steroid hormone metabolism. They modulate the conversion of active hormones to their inactive forms and vice versa affecting the cellular concentration of these hormones. The proteins do not function as part of a larger complex but influence multiple biochemical processes through their enzymatic actions. Their roles in the regulation of sex steroids are important for maintaining normal cellular activity and tissue homeostasis.
Pathways
AKR1C1 and AKR1C2 are involved in intricate steroid hormone signaling and metabolism pathways. They engage with the androgen and estrogen receptor signaling pathways by modulating hormone availability. The interplay with enzymes like 5-alpha reductase and aromatase highlights their role in the balance of active and inactive hormone forms within these pathways. Their function can influence cellular proliferation and differentiation processes within different tissues.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Journal of neuroinflammation 22:74 PubMed40069860
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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