Mouse Recombinant Monoclonal SMAD2 antibody. Suitable for IHC-P, WB and reacts with Rat, Mouse, Human samples.
IgG1
Mouse
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Liquid
Monoclonal
IHC-P | WB | ICC/IF | IP | |
---|---|---|---|---|
Human | Tested | Tested | Not recommended | Not recommended |
Mouse | Tested | Tested | Not recommended | Not recommended |
Rat | Tested | Tested | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/100 - 1/250 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Mouse | Dilution info 1/100 - 1/250 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Human | Dilution info 1/100 - 1/250 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/1000 | Notes - |
Species Mouse | Dilution info 1/1000 | Notes - |
Species Human | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat, Human, Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Rat, Mouse | Dilution info - | Notes - |
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. Promotes TGFB1-mediated transcription of odontoblastic differentiation genes in dental papilla cells (PubMed:33548622). Positively regulates PDPK1 kinase activity by stimulating its dissociation from the 14-3-3 protein YWHAQ which acts as a negative regulator (By similarity).
Madh2, Madr2, Madh2, Madr2, Smad2, Mothers against decapentaplegic homolog 2, MAD homolog 2, Mothers against DPP homolog 2, Mad-related protein 2, SMAD family member 2, mMad2, SMAD 2, Smad2
Mouse Recombinant Monoclonal SMAD2 antibody. Suitable for IHC-P, WB and reacts with Rat, Mouse, Human samples.
IgG1
Mouse
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Liquid
Monoclonal
18-Smad2-3
Affinity purification Protein A
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
This supplementary information is collated from multiple sources and compiled automatically.
Smad2 and Smad3 also known as Smad family member 2 and Smad family member 3 are intracellular proteins involved in signaling cascades. Smad2 has a molecular mass of approximately 58 kDa and Smad3 is around 52 kDa. These proteins are part of the Smad family which functions in the signal transduction for the Transforming Growth Factor-beta (TGF-β) superfamily. Smad2 and Smad3 are widely expressed in many tissues including the brain heart and lung suggesting their broad biological roles.
Smad2 and Smad3 regulate transcriptional responses essential for cellular processes including proliferation differentiation and apoptosis. These proteins form a trimeric complex with Smad4 upon activation by TGF-β receptors. The activated complex translocates into the nucleus where it binds to DNA and influences gene expression. Such actions highlight their fundamental role in controlling cell behavior and fate.
Smad2 and Smad3 play critical roles within the TGF-β signaling pathway. This pathway has significant effects on cell cycle control and immune regulation. Both Smad2 and Smad3 interact closely with the protein Smad4 to mediate various downstream effects integrating signals with other pathways such as MAPK pathway which involves different cellular responses.
Smad2 and Smad3 are closely associated with cancer and fibrosis. Aberrant TGF-β signaling often leads to tumor progression and metastasis partly due to the dysregulated actions of Smad2 and Smad3. Additionally these proteins through their pathway functions contribute to the pathological process of fibrosis in organs like the liver and lungs. It is important to note their interaction with the ERK protein which can also influence disease outcomes in these contexts.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Immunohistochemical analysis of paraffin-embedded rat colon tissue labeling Smad2 + Smad3 with ab305325 at 1/250 dilution (3.756 ug/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat colon is observed.
The section was incubated with ab305325 for 30 mins at room temperature, followed by anti-mouse IgG1 antibody (Rabbit monoclonal [M1gG51-4] Anti-Mouse IgG1 H&L ab125913) for 8 mins during the LeicaDS9800 kit staining procedure. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is 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.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 18809571).
The identity of the band around 37 kDa is unknown.
Exposure times: Lanes 1, 4 and 5: 180 seconds; Lanes 2 and 3: 37 seconds.
All lanes: Western blot - Anti-Smad2 + Smad3 antibody [18/Smad2/3] (ab305325) at 1/1000 dilution
Lane 1: HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate 20 μg
Lane 2: A549 (human lung carcinoma epithelial cell), whole cell lysate 20 μg
Lane 3: HT-1080 (human fibrosarcoma epithelial cell), whole cell lysate 20 μg
Observed band size: 58 kDa, 62 kDa
Exposure time: 114s
Immunohistochemical analysis of paraffin-embedded mouse breast cancer tissue labeling Smad2 + Smad3 with ab305325 at 1/250 dilution (3.756 ug/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse breast cancer is observed.
The section was incubated with ab305325 for 30 mins at room temperature, followed by anti-mouse IgG1 antibody (Rabbit monoclonal [M1gG51-4] Anti-Mouse IgG1 H&L ab125913) for 8 mins during the LeicaDS9800 kit staining procedure. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is 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.
Immunohistochemical analysis of paraffin-embedded human colon tissue labeling Smad2 + Smad3 with ab305325 at 1/100 dilution (9.39 ug/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human colon is observed.
The section was incubated with ab305325 for 30 mins at room temperature, followed by anti-mouse IgG1 antibody (Rabbit monoclonal [M1gG51-4] Anti-Mouse IgG1 H&L ab125913) for 8 mins during the LeicaDS9800 kit staining procedure. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is 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.
Immunohistochemical analysis of paraffin-embedded human colon cancer tissue labeling Smad2 + Smad3 with ab305325 at 1/100 dilution (9.39 ug/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human colon cancer is observed.
The section was incubated with ab305325 for 30 mins at room temperature, followed by anti-mouse IgG1 antibody (Rabbit monoclonal [M1gG51-4] Anti-Mouse IgG1 H&L ab125913) for 8 mins during the LeicaDS9800 kit staining procedure. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is 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.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 18809571).
The identity of the band around 37 kDa is unknown.
Exposure time: 59 seconds.
All lanes: Western blot - Anti-Smad2 + Smad3 antibody [18/Smad2/3] (ab305325) at 1/1000 dilution
Lane 1: RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate 10 μg
Lane 2: C2C12 (mouse myoblasts myoblast), whole cell lysate 10 μg
Lane 3: C6 (rat glial tumor glial cell), whole cell lysate 10 μg
Observed band size: 58 kDa, 62 kDa
Exposure time: 59s
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Exposure time: 15 seconds.
All lanes: Western blot - Anti-Smad2 + Smad3 antibody [18/Smad2/3] (ab305325) at 1/1000 dilution
Lane 1: His-tagged human Smad2 recombinant protein fragment 10ng
Lane 2: His/GST-tagged human Smad3 recombinant protein fragment 10ng
Observed band size: 37 kDa, 60 kDa
Exposure time: 15s
Immunohistochemical analysis of paraffin-embedded mouse colon tissue labeling Smad2 + Smad3 with ab305325 at 1/250 dilution (3.756 ug/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse colon is observed.
The section was incubated with ab305325 for 30 mins at room temperature, followed by anti-mouse IgG1 antibody (Rabbit monoclonal [M1gG51-4] Anti-Mouse IgG1 H&L ab125913) for 8 mins during the LeicaDS9800 kit staining procedure. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is 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.
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