Anti-Smad2 (phospho S250) antibody [EPR2855(2)]
- BOND RX™ Validated
- 20ul selling size
- RabMAb
- Recombinant
- KO Validated
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(8 Publications)
Rabbit Recombinant Monoclonal SMAD2 phospho S250 antibody. Suitable for WB, Flow Cyt (Intra), IHC-P and reacts with Human, Mouse samples. Cited in 8 publications.
View Alternative Names
MADH2, MADR2, SMAD2, SMAD family member 2, SMAD 2, hSMAD2, JV18-1, Mad-related protein 2, Mothers against decapentaplegic homolog 2, hMAD-2, MAD homolog 2, Mothers against DPP homolog 2
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (AB184557)
Intracellular flow cytometric analysis of2% paraformaldehyde-fixed and permeabilized HeLa cells labeling Smad2 (phospho S250) with ab184557 at 1/20 dilution (red) compared to a Rabbit monoclonal IgG isotype control (green), followed by Goat anti rabbit IgG (FITC) secondary antibody at 1/150 dilution. HeLa cells labeled using ab184557 preincubated with Smad2 (phospho S250) peptide (blue) or non-phospho-Smad2 peptide (orange).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (AB184557)
Immunohistochemical analysis of paraffin-embedded human endometrial carcinoma tissue labeling Smad2 (phospho S250) with ab184557 at 1/1000 dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on human endometrial carcinoma without alkaline phosphatase treatment (image A). No signal was detected when tissues were treated with alkaline phosphatase (image B).
The section was incubated with ab184557 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (AB184557)
Immunohistochemical analysis of paraffin-embedded human colon tissue labeling Smad2 (phospho S250) with ab184557 at 1/1000 dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on human colon without alkaline phosphatase treatment (image A). No signal was detected when tissues were treated with alkaline phosphatase (image B).
The section was incubated with ab184557 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (AB184557)
Immunohistochemical analysis of paraffin-embedded mouse lung cancer tissue labeling Smad2 (phospho S250) with ab184557 at 1/1000 dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on mouse lung cancer without alkaline phosphatase treatment (image A). No signal was detected when tissues were treated with alkaline phosphatase (image B).
The section was incubated with ab184557 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- WB
Lab
Western blot - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (AB184557)
In Western blot, ab184557 was shown to bind specifically to SMAD2. Target of interest was observed at 58 kDa in wild-type HeLa cell lysates (lane 1) with no signal observed at this size in SMAD2 knockout cell line (lane 2) (lane 2, knockout cell line ab255430).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (ab184557) at 1/1000 dilution
Lane 1:
Wild-type HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
SMAD2 knockout HeLa 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: 58 kDa
false
Exposure time: 10s
- WB
Supplier Data
Western blot - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (AB184557)
All lanes:
Western blot - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (ab184557) at 1/1000 dilution
Lane 1:
untreated HeLa cells lysates at 10 µg
Lane 2:
HeLa cell lysate treated with alkaline phosphatase at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution
Predicted band size: 52 kDa
Observed band size: 58 kDa
false
- WB
Lab
Western blot - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (AB184557)
The expression of Smad2 (phospho S250) is upregulated in response to PMA treatment.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Smad2 (phospho S250) antibody [EPR2855(2)] (ab184557) at 1/1000 dilution
Lane 1:
Untreated NIH/3T3 (mouse embryonic fibroblast) whole cell lysate (untreated membrane) at 20 µg
Lane 2:
NIH/3T3 treated with 200nM PMA for 30 minutes whole cell lysate (untreated membrane) at 20 µg
Lane 3:
Untreated NIH/3T3 (mouse embryonic fibroblast) whole cell lysate (alkaline phosphatase treated membrane) at 20 µg
Lane 4:
NIH/3T3 treated with 200nM PMA for 30 minutes whole cell lysate (alkaline phosphatase treated membrane) 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: 58 kDa
false
Exposure time: 10s
Related conjugates and formulations (1)
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Anti-Smad2 (phospho S250) antibody [EPR2855(2)] - 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
Smad2 acts as an intracellular mediator for TGF-β signaling a pathway important for regulating cell proliferation differentiation and apoptosis. Smad2 typically functions as part of a heteromeric complex with Smad4 another key player in TGF-β signaling. Upon activation phosphorylated Smad2 combines with Smad4 to form a complex that translocates into the nucleus. This complex then binds to specific DNA sequences to regulate the transcription of target genes involved in processes such as cell growth inhibition and extracellular matrix production.
Pathways
Smad2 is integral to the TGF-β and activin receptor signaling pathways. These pathways are essential in controlling cell growth and immune responses. Smad2 interacts with other proteins such as Smad3 in addition to Smad4 to modulate gene expression effectively. The interaction between Smad2 and these proteins ensures precise control of cellular responses to external stimuli emphasizing its pivotal role in maintaining cellular homeostasis.
Product protocols
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Target data
Publications (8)
Recent publications for all applications. Explore the full list and refine your search
International journal of molecular sciences 26: PubMed39941126
2025
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Unspecified application
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Unspecified reactive species
Endocrinology 162: PubMed33955458
2021
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Unspecified reactive species
Therapeutic advances in chronic disease 12:2040622320987348 PubMed33948156
2021
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Unspecified reactive species
Molecular medicine reports 23: PubMed33760134
2021
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Unspecified application
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Unspecified reactive species
Brazilian journal of medical and biological resear 54:e9206 PubMed33503202
2021
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Unspecified application
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Unspecified reactive species
Molecular medicine reports 20:2667-2674 PubMed31524262
2019
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Unspecified reactive species
Aging 11:3298-3314 PubMed31147529
2019
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Unspecified application
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Unspecified reactive species
American journal of translational research 9:591-600 PubMed28337286
2017
Applications
WB
Species
Human
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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