Anti-Smad2 (phospho S250) 抗体 [EPR26263-58] (ab300079)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR26263-58] to Smad2 (phospho S250)
- Suitable for: WB, Dot blot, IP, ICC/IF
- Knockout validated
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
製品の概要
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製品名
Anti-Smad2 (phospho S250) antibody [EPR26263-58]
Smad2 一次抗体 製品一覧 -
製品の詳細
Rabbit monoclonal [EPR26263-58] to Smad2 (phospho S250) -
由来種
Rabbit -
アプリケーション
適用あり: WB, Dot blot, IP, ICC/IFmore details
適用なし: Flow Cyt (Intra) or IHC-P -
種交差性
交差種: Mouse, Rat, Human -
免疫原
This product was produced with the following immunogens:
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers. -
ポジティブ・コントロール
- WB: Whole cell lysates: Parental HeLa (human cervix adenocarcinoma epithelial cell) untreated and treated with 0.2µM PMA for 0.5h, NIH/3T3 untreated and treated with 0.2µM PMA for 0.5h, Untreated and treated with 0.2µM PMA for 0.5h C6 (rat glial tumor glial cell), HeLa treated with 0.2µM PMA for 0.5h (Untreated membrane ). ICC/IF: HeLa IP: HeLa and HIH/3T3 treated with 0.2µM PMA for 0.5h. DB: Smad2 peptides phosphorylated at: S245+S250+S255 a, S245+S250+S255 b, S245+S250, S250+S255, S250 only.
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特記事項
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
製品の特性
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製品の状態
Liquid -
保存方法
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. -
バッファー
pH: 7.20
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA -
Concentration information loading...
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精製度
Protein A purified -
ポリ/モノ
モノクローナル -
クローン名
EPR26263-58 -
アイソタイプ
IgG -
研究分野
関連製品
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Alternative Versions
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Related Products
- VeriBlot for IP Detection Reagent (HRP) (ab131366)
- Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)
- Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730)
- Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (ab195889)
- Goat Anti-Rabbit IgG H&L (HRP) (ab97051)
アプリケーション
The Abpromise guarantee
Abpromise保証は、 次のテスト済みアプリケーションにおけるab300079の使用に適用されます
アプリケーションノートには、推奨の開始希釈率がありますが、適切な希釈率につきましてはご検討ください。
アプリケーション | Abreviews | 特記事項 |
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WB |
1/1000. Detects a band of approximately 65 kDa (predicted molecular weight: 52 kDa).
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Dot blot |
1/1000.
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IP |
1/30.
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ICC/IF |
1/50.
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特記事項 |
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WB
1/1000. Detects a band of approximately 65 kDa (predicted molecular weight: 52 kDa). |
Dot blot
1/1000. |
IP
1/30. |
ICC/IF
1/50. |
ターゲット情報
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機能
Receptor-regulated SMAD (R-SMAD) that is an intracellular signal transducer and transcriptional modulator activated by TGF-beta (transforming growth factor) and activin type 1 receptor kinases. Binds the TRE element in the promoter region of many genes that are regulated by TGF-beta and, on formation of the SMAD2/SMAD4 complex, activates transcription. May act as a tumor suppressor in colorectal carcinoma. -
組織特異性
Expressed at high levels in skeletal muscle, heart and placenta. -
配列類似性
Belongs to the dwarfin/SMAD family.
Contains 1 MH1 (MAD homology 1) domain.
Contains 1 MH2 (MAD homology 2) domain. -
翻訳後修飾
Phosphorylated on one or several of Thr-220, Ser-245, Ser-250, and Ser-255. In response to TGF-beta, phosphorylated on Ser-465/467 by TGF-beta and activin type 1 receptor kinases. Able to interact with SMURF2 when phosphorylated on Ser-465/467, recruiting other proteins, such as SNON, for degradation. In response to decorin, the naturally occurring inhibitor of TGF-beta signaling, phosphorylated on Ser-240 by CaMK2. Phosphorylated by MAPK3 upon EGF stimulation; which increases transcriptional activity and stability, and is blocked by calmodulin.
In response to TGF-beta, ubiquitinated by NEDD4L; which promotes its degradation.
Acetylated on Lys-19 by coactivators in response to TGF-beta signaling, which increases transcriptional activity. Isoform short: Acetylation increases DNA binding activity in vitro and enhances its association with target promoters in vivo. Acetylation in the nucleus by EP300 is enhanced by TGF-beta. -
細胞内局在
Cytoplasm. Nucleus. Cytoplasmic and nuclear in the absence of TGF-beta. On TGF-beta stimulation, migrates to the nucleus when complexed with SMAD4. On dephosphorylation by phosphatase PPM1A, released from the SMAD2/SMAD4 complex, and exported out of the nucleus by interaction with RANBP1. - Information by UniProt
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参照データベース
- Entrez Gene: 4087 Human
- Entrez Gene: 17126 Mouse
- Entrez Gene: 29357 Rat
- Omim: 601366 Human
- SwissProt: Q15796 Human
- SwissProt: Q62432 Mouse
- SwissProt: O70436 Rat
- Unigene: 12253 Human
see all -
別名
- Drosophila, homolog of, MADR2 antibody
- hMAD-2 antibody
- HsMAD2 antibody
see all
画像
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All lanes : Anti-Smad2 (phospho S250) antibody [EPR26263-58] (ab300079) at 1/1000 dilution
Lane 1 : Untreated parental HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate
Lane 2 : Parental HeLa treated with 0.2µM PMA for 0.5h whole cell lysate
Lane 3 : Untreated SAMD2 KO Hela whole cell lysate
Lane 4 : SAMD2 KO Hela treated with 0.2µM PMA for 0.5h whole cell lysate
Lysates/proteins at 30 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 52 kDa
Observed band size: 62 kDa why is the actual band size different from the predicted?
Exposure time: 10 seconds5% NFDM/TBST was used as blocking and diluting buffer.
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All lanes : Anti-Smad2 (phospho S250) antibody [EPR26263-58] (ab300079) at 1/1000 dilution
Lane 1 : Untreated NIH/3T3 (Mouse embryonic fibroblast) whole cell lysate
Lane 2 : NIH/3T3 treated with 0.2µM PMA for 0.5h whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 52 kDa
Observed band size: 65 kDa why is the actual band size different from the predicted?
Exposure time: 180 seconds5% NFDM/TBST was used as blocking and diluting buffer.
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All lanes : Anti-Smad2 (phospho S250) antibody [EPR26263-58] (ab300079) at 1/1000 dilution
Lane 1 : Untreated C6 (rat glial tumor cell) whole cell lysate
Lane 2 : C6 treated with 0.2µM PMA for 0.5h whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 52 kDa
Observed band size: 65 kDa why is the actual band size different from the predicted?
Exposure time: 180 seconds5% NFDM/TBST was used as blocking and diluting buffer.
Bands around and below the 50-kDa marker could be degradation fragments.
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All lanes : Anti-Smad2 (phospho S250) antibody [EPR26263-58] (ab300079) at 1/1000 dilution
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell) treated with 0.2µM PMA for 0.5h (Untreated membrane) whole cell lysate
Lane 2 : HeLa treated with 0.2µM PMA for 0.5h (phosphatase treated membrane) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 52 kDa
Observed band size: 65 kDa why is the actual band size different from the predicted?
Exposure time: 180 seconds5% NFDM/TBST was used as blocking and diluting buffer.
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Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells lebeling Smad2 (phospho S250) with ab300079 at 1/50 (10.8 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 µg/mL) dilution (Green). Confocal image showing increased cytoplasm and nuclear staining in HeLa cells treated with PMA (200 nM ) for 30 min. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5 µg/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control: Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 µg/mL) dilution.
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Smad2 (phospho S250) was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) treated with 0.2µM PMA for 0.5h whole cell lysate with ab300079 at 1/30 dilution (2 µg in 0.35 mg lysates). Western blot was performed on the immunoprecipitate using ab300079 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1: HeLa (human cervix adenocarcinoma epithelial cell) treated with 0.2µM PMA for 0.5h whole cell lysate 10 µg (Inset)
Lane 2: ab300079 in HeLa treated with 0.2µM PMA for 0.5h whole cell lysate
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab300079 in HeLa treated with 0.2µM PMA for 0.5h whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 10 seconds
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Smad2 (phospho S250) was immunoprecipitated from 0.35 mg NIH/3T3 treated with 0.2µM PMA for 0.5h whole cell lysate with ab300079 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300079 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1: NIH/3T3 treated with 0.2µM PMA for 0.5h whole cell lysate 20 µg (Inset)
Lane 2: ab300079 in NIH/3T3 treated with 0.2µM PMA for 0.5h whole cell lysate
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab300079 in NIH/3T3 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 10 seconds
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Dot blot analysis of Smad2 (phospho S250) using ab300079 at 1:1000 (0.54 µg/ml), followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1:100,000 dilution.
Lane 1: Smad2 (phospho S245+S250+S255) peptide a
Lane 2: Smad2 (phospho S245+S250+S255) peptide b
Lane 3: Smad2 (phospho S245+S250) peptide
Lane 4: Smad2 (phospho S245+S255) peptide
Lane 5: Smad2 (phospho S250+S255) peptide
Lane 6: Smad2 (phospho S245) peptideLane 7: Smad2 (phospho S250) peptide
Lane 8: Smad2 (phospho S255) peptide
Lane 9: Smad2 non-phospho peptideExposure time: 3 minutes
Blocking and diluting buffer and concentration: 5% NFDM/TBST
プロトコール
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
データシートおよび資料
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SDS download
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Datasheet download
Certificate of Compliance
参考文献 (2)
ab300079 は 2 報の論文で使用されています。
- Wang W et al. Antifibrotic Effects of Tetrahedral Framework Nucleic Acids by Inhibiting Macrophage Polarization and Macrophage-Myofibroblast Transition in Bladder Remodeling. Adv Healthc Mater 12:e2203076 (2023). PubMed: 36603196
- Liu F et al. Decreased DANCR contributes to high glucose-induced extracellular matrix accumulation in human renal mesangial cell via regulating the TGF-β/Smad signaling. FASEB J 37:e22926 (2023). PubMed: 37052733