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Anti-Protein phosphotase inhibitor 1 antibody [EP902Y]
See all Protein phosphotase inhibitor 1 products (2) ...
Rabbit monoclonal [EP902Y] to Protein phosphotase inhibitor 1
WB, IP, Flow Cyt, ICC/IF, IHC-Pmore details
Reacts with
Mouse, Rat, Human
Synthetic peptide corresponding to residues in the N-terminus of human Protein phosphotase inhibitor 1.
Brain tissue/lysate
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.01% Sodium Azide
Constituents: 40% Glycerol, 0.05% BSA, 0.15M Sodium chloride, 50mM Tris glycine, pH 7.4
Tissue culture supernatant
Monoclonal
EP902Y
IgG
Western blot - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)
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Immunohistochemistry (Paraffin-embedded sections) - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)
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Immunocytochemistry/ Immunofluorescence-Protein phosphotase inhibitor 1 antibody [EP902Y](ab40877)
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Our Abpromise guarantee covers the use of ab40877 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/100000Detects a band of approximately 27 kDa (predicted molecular weight: 19 kDa).
IP: 1/50
Flow Cyt: 1/20
ICC/IF: Use a concentration of 5 µg/ml
IHC-P: 1/100 - 1/250.
Inhibitor of protein-phosphatase 1. This protein may be important in hormonal control of glycogen metabolism. Hormones that elevate intracellular cAMP increase I-1 activity in many tissues. I-1 activation may impose cAMP control over proteins that are not directly phosphorylated by PKA. Following a rise in intracellular calcium, I-1 is inactivated by calcineurin (or PP2B). Does not inhibit type-2 phosphatases.
Belongs to the protein phosphatase inhibitor 1 family.
Phosphorylation of Thr-35 is required for activity.
Target information above from: UniProt accessionQ13522
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)
![Western blot - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)](/ps/datasheet/Images/40/ab40877/ab40877wb.jpg)
Anti-Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877) at 1/40000 dilution + Rat brain at 10 µg
Predicted band size : 19 kDa
Observed band size : 27 kDa (why is the actual band size different from the predicted?)
Immunohistochemistry (Paraffin-embedded sections) - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)
![Immunohistochemistry (Paraffin-embedded sections) - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)](/ps/datasheet/Images/40/ab40877/ab40877IHCP.jpg)
Immunohistochemical analysis of paraffin-embedded human normal brain tissue using ab40877 diluted 1:100.
Immunocytochemistry/ Immunofluorescence-Protein phosphotase inhibitor 1 antibody [EP902Y](ab40877)
](/ps/datasheet/images/40/ab40877/Protein-phosphotase-inhibitor-1-Primary-antibodies-ab40877-1.jpg)
ICC/IF image of ab40877 stained PC12 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab40877, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
Flow Cytometry-Protein phosphotase inhibitor 1 antibody [EP902Y](ab40877)
](/ps/datasheet/images/40/ab40877/Protein-phosphotase-inhibitor-1-Primary-antibodies-ab40877-2.jpg)
Overlay histogram showing SH-SY5Y cells stained with ab40877 (red line). The cells were fixed with 4% paraformaldehyde (10 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 (ab40877, 1/20 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 IgG (monoclonal) ( 1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in SH-SY5Y cells fixed with 80% methanol/permeabilized in 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See all 2 publications for this product
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![Western blot - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)](/ps/datasheet/Images/40/ab40877/ab40877wb.jpg)
Anti-Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877) at 1/40000 dilution + Rat brain at 10 µg
Predicted band size : 19 kDa
Observed band size : 27 kDa (why is the actual band size different from the predicted?)
![Immunohistochemistry (Paraffin-embedded sections) - Protein phosphotase inhibitor 1 antibody [EP902Y] (ab40877)](/ps/datasheet/Images/40/ab40877/ab40877IHCP.jpg)
Immunohistochemical analysis of paraffin-embedded human normal brain tissue using ab40877 diluted 1:100.
](/ps/datasheet/images/40/ab40877/Protein-phosphotase-inhibitor-1-Primary-antibodies-ab40877-1.jpg)
ICC/IF image of ab40877 stained PC12 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab40877, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
](/ps/datasheet/images/40/ab40877/Protein-phosphotase-inhibitor-1-Primary-antibodies-ab40877-2.jpg)
Overlay histogram showing SH-SY5Y cells stained with ab40877 (red line). The cells were fixed with 4% paraformaldehyde (10 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 (ab40877, 1/20 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
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