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Products:Signal Transduction >> Signaling Pathway >> Nuclear Signaling >> SMADs
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Read our guarantee »Anti-SMAD5 antibody [EP619Y]
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Rabbit monoclonal [EP619Y] to SMAD5
IHC-P, WB, ICC, Flow Cytmore details
Reacts with
Rat, Human, African Green Monkey
Predicted to work with
Mouse
Synthetic peptide corresponding to residues near the MH2 domain of human SMAD5.
Cos-1 cell lysate.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%
Concentration information loading...
Protein A purified
Monoclonal
EP619Y
IgG
Our Abpromise guarantee covers the use of ab40771 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: Use a concentration of 4 µg/ml.
WB: 1/1000. Detects a band of approximately 52 kDa (predicted molecular weight: 52 kDa).
ICC: 1/50.
Flow Cyt: 1/30 - 1/50.
Transcriptional modulator activated by BMP (bone morphogenetic proteins) type 1 receptor kinase. SMAD5 is a receptor-regulated SMAD (R-SMAD).
Ubiquitous.
Belongs to the dwarfin/SMAD family.
Contains 1 MH1 (MAD homology 1) domain.
Contains 1 MH2 (MAD homology 2) domain.
Phosphorylated on serine by BMP (bone morphogenetic proteins) type 1 receptor kinase.
Ubiquitin-mediated proteolysis by SMAD-specific E3 ubiquitin ligase SMURF1.
Cytoplasm. Nucleus. Cytoplasmic in the absence of ligand. Migrates to the nucleus when complexed with SMAD4.
Target information above from: UniProt accessionQ99717
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - SMAD5 antibody [EP619Y] (ab40771)
![Western blot - SMAD5 antibody [EP619Y] (ab40771)](/ps/datasheet/Images/40/ab40771/ab40771.bmp)
Anti-SMAD5 antibody [EP619Y] (ab40771) at 1/1000 dilution + Cos-1 cell lysate at 10 µg
Predicted band size : 52 kDa
Observed band size : 52 kDa
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)-SMAD5 antibody [EP619Y](ab40771)
](/ps/datasheet/images/40/ab40771/SMAD5-Primary-antibodies-ab40771-1.jpg)
ab40771 (4µg/ml) staining SMAD5 in human skin using an automated system (DAKO Autostainer Plus). Using this protocol there is strong staining of nuclear/cytoplasmic compartments within the stratum granulosum.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
Flow Cytometry-SMAD5 antibody [EP619Y](ab40771)
](/ps/datasheet/images/40/ab40771/SMAD5-Primary-antibodies-ab40771-2.jpg)
Overlay histogram showing HEK293 cells stained with ab40771 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab40771, 1/50 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit monoclonal IgG (1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HEK293 cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
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](/ps/datasheet/images/40/ab40771/SMAD5-Primary-antibodies-ab40771-1.jpg)
ab40771 (4µg/ml) staining SMAD5 in human skin using an automated system (DAKO Autostainer Plus). Using this protocol there is strong staining of nuclear/cytoplasmic compartments within the stratum granulosum.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
](/ps/datasheet/images/40/ab40771/SMAD5-Primary-antibodies-ab40771-2.jpg)
Overlay histogram showing HEK293 cells stained with ab40771 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab40771, 1/50 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
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