P3717
Phosphoserine-BSA
2 mg/mL, buffered aqueous solution
Synonym(s):
Phosphoserine Antibody Inhibitor
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40 EA
CN¥9,720.40
About This Item
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sterility
non-sterile
Quality Level
form
buffered aqueous solution
concentration
2 mg/mL
shipped in
dry ice
storage temp.
−20°C
1 of 4
This Item | P3842 | P3967 | SRP0204 |
|---|---|---|---|
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level - |
| form buffered aqueous solution | form buffered aqueous solution | form buffered aqueous solution | form aqueous solution |
| sterility non-sterile | sterility - | sterility non-sterile | sterility - |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. −70°C |
| concentration 2 mg/mL | concentration 2 mg/mL | concentration 2 mg/mL | concentration >0.02 mg/mL |
| shipped in dry ice | shipped in dry ice | shipped in dry ice | shipped in dry ice |
General description
The activity of proteins depends on phosphorylation of specific amino acid residues. In applications involving identification of activated cellular proteins, it is important to confirm specificity of antibodies used against a particular phosphorylated amino acid. For such applications, inhibitors of phosphorylated antibodies on specific amino acid residues are suitable. Phosphoserine antibody inhibitor may be used for the specific inhibition of the reactivity of anti-phosphoserine antibodies but not that of anti-phosphothreonine- or anti-phosphotyrosine-specific antibodies.
Specificity
O-phospho-L-serine conjugated to bovine serum albumin. Phosphoserine antibody inhibitor specifically blocks the reactivity of anti-phosphoserine antibody. It does not block the activity of anti-phosphothreonine or anti-phosphotyrosine-specific antibodies. The product is useful in immunoblotting and in ELISA.
Working dilution is at least 2 μg/ml by the specific inhibition of the reactivity of Monoclonal Anti-Phosphoserine (Sigma Product No. P3430), used in immunoblotting of rat cerebral cortex extract, and in ELISA.
Working dilution is at least 2 μg/ml by the specific inhibition of the reactivity of Monoclonal Anti-Phosphoserine (Sigma Product No. P3430), used in immunoblotting of rat cerebral cortex extract, and in ELISA.
Application
Phosphoserine-BSA may be used for specific inhibition of monoclonal anti-phosphoserine (Sigma Product No. P3430) in immunoblotting and ELISA applications, at a working dilution of 2 μg/mL.
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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Birte Schulenberg et al.
Electrophoresis, 25(15), 2526-2532 (2004-08-10)
Protein phosphorylation plays a vital role in the regulation of most aspects of cellular activity, being key to propagating messages within signal transduction pathways and to modulating protein function. Pro-Q Diamond phosphoprotein gel stain is suitable for the fluorescence detection
Motoyuki Ogawa et al.
Biochemical and biophysical research communications, 304(4), 676-683 (2003-05-03)
Paxillin has been recognized as a focal adhesion adapter protein that participates in the integrin-mediated signaling. An earlier study [Ogawa et al. Biochim. Biophys. Acta 1519 (2001) 235] found that frog paxillin was expressed in the kidney epithelial cell line
Matthew G Vander Heiden et al.
Science (New York, N.Y.), 329(5998), 1492-1499 (2010-09-18)
Proliferating cells, including cancer cells, require altered metabolism to efficiently incorporate nutrients such as glucose into biomass. The M2 isoform of pyruvate kinase (PKM2) promotes the metabolism of glucose by aerobic glycolysis and contributes to anabolic metabolism. Paradoxically, decreased pyruvate
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