产品名称
Phosphothreonine-BSA, 2 mg/mL, buffered aqueous solution
form
buffered aqueous solution
concentration
2 mg/mL
shipped in
dry ice
storage temp.
−20°C
Quality Level
Application
Phosphothreonine-BSA can be used in various immunochemical assays like ELISA and immunoblotting for the specific inhibition of the reactivity of anti-phosphothreonine antibodies.
Phosphothreonine-BSA has been used in Pro-Q Diamond phosphoprotein gel staining method to detect phosphoamino acids.
Biochem/physiol Actions
O-phospho-L-threonine conjugated to bovine serum albumin. Phosphothreonine antibody inhibitor specifically blocks the reactivity of anti-phosphothreonine antibody. It does not block the activity of anti-phosphotyrosine or anti-phosphoserine-specific antibodies.
Working dilution is at least 10 μg/ml by the specific inhibition of the reactivity of Monoclonal Anti-Phosphothreonine (Sigma Product No. P 3555) in ELISA.
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.
General description
Phosphothreonine-BSA is a Phosphothreonine antibody inhibitor which blocks the reactivity of anti-phosphothreonine antibody. Antibodies against phosphorylated amino acid can be used as a tool for identification, quantification and immunoaffinity isolation of activated cellular proteins. The product specifically blocks the reactivity of anti-phosphothreonine antibody but does not block anti-phosphoserine- or anti-phosphotyrosine specific antibodies.
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Characterization of dynamic and steady-state protein phosphorylation using a fluorescent phosphoprotein gel stain and mass spectrometry
Schulenberg B, et al.
Electrophoresis, 25(15), 2526-2532 (2004)
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
相关内容
Datasheet
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持