Anti-Phosphoserine antibody is a rabbit polyclonal antibody that is used to detect Phosphoserine in western blot. Suitable for chemical samples.
- Recognize proteins phosphorylated on serine residues
- Does not cross-react with phosphotyrosine
- Cited in over 150 publications
- Trusted since 2002
pH: 6 - 8
Preservative: 0.1% Sodium azide
Constituents: 50% Glycerol (glycerin, glycerine), 49.9% PBS
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Chemical | Tested |
Species | Dilution info | Notes |
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Species Chemical | Dilution info - | Notes To block use 3%BSA with 0.1% gelatin (do not use milk). We recommend that the antibody solution should contain 0.5% BSA to prevent non-specific binding. |
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PS, pSER, phospho-Ser
Anti-Phosphoserine antibody is a rabbit polyclonal antibody that is used to detect Phosphoserine in western blot. Suitable for chemical samples.
- Recognize proteins phosphorylated on serine residues
- Does not cross-react with phosphotyrosine
- Cited in over 150 publications
- Trusted since 2002
pH: 6 - 8
Preservative: 0.1% Sodium azide
Constituents: 50% Glycerol (glycerin, glycerine), 49.9% PBS
Recognize proteins phosphorylated on serine residues. Does not cross-react with phosphotyrosine. Will detect 50 ng of phosvitin with immunoblotting or 0.5 ng of phosvitin with immunocaptured ELISA.Antibody slightly cross-reacts with phosphothreonine (about 20%) based on indirect ELISA data.
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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.
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Blocking Step: 10% Milk for 1 hour at room temperature
All lanes: Western blot - Anti-Phosphoserine antibody (ab9332) at 3 µg/mL
All lanes: Whole cell lysate of monkey COS7 cells at 25 µg
All lanes: An HRP-conjugated Pig anti-rabbit IgG polyclonal at 1/3000 dilution
Western blotting of a melanoma cell lysate with anti-phosphoserine antibodies
The detected band is 53 kD, and is a similar size to the p53 tumor suppressor factor.
The cells were treated with 0, 50, 200 or 400 J UV (lane A to D, respectively) and with 0.1uM of okadaic acid(lane E). Actin level was measured as an internal standard of cell protein.
Western blotting of a melanoma cell lysate with anti-phosphoserine antibodies.
The detected band is 53 kD, and is a similar size to the p53 tumor suppressor factor.
The cells were treated with 0, 50, 200 or 400 J UV (lane A to D, respectively) and with 0.1uM of okadaic acid (lane E). Actin level was measured as an internal standard of cell protein.
Lane 1: Western blot - Biotin Anti-Phosphoserine antibody (Biotin Anti-Phosphoserine antibody ab9335)
Lane 1: Western blot - Anti-Phosphoserine antibody (ab9332)
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