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Anti-Phosphoserine antibody [PSR-45]
See all Phosphoserine products (8) ...
Mouse monoclonal [PSR-45] to Phosphoserine
Monoclonal Anti-Phosphoserine reacts against phosphorylated serine both as free amino acid or when conjugated to carriers such as BSA or KLH. No cross-reactivity is observed with non-phosphorylated serine, phosphothreonine, phosphotyrosine, AMP or ATP.
IP, Indirect ELISA, WBmore details
WB: rat brain cortex lysate ( a main 50kDa band is seen by detection with biotin-avidin AEC staining) ELISA: phosphoserine conjugated to BSA
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
0.01M Na phosphate, 0.25M NaCl, pH7.6, 0.05% Na azide, 0.01% Thimerisol, 15mg/ml BSA
Concentration information loading...
Ascites
Monoclonal
PSR-45
IgG1
unknown
Neuroscience >> Neurotransmission >> Intracellular Signaling >> Regulation
Signal Transduction >> Protein Phosphorylation >> pSer / pThr
Signal Transduction >> Metabolism >> Amino Acids
Our Abpromise guarantee covers the use of ab6639 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IP: 1/2000
I-ELISA: 1/4000
WB: 1/500 - 1/1000.Can be blocked with Phosphoserine protein (ab100812). (Do not use milk as a blocking agent or in diluents, as milk casein is phosphorylated at several serine residues. BSA is recommended instead. Stronger blocking agent percentage is recommended (e.g. 10%), in addition to varying loading amounts and shorter incubation time (1-2h RT))
Changes in the serine/threonine phosphorylation state of a protein in response to various external stimuli can have profound effects on cellular signal transduction, apoptosis and carcinogenesis. The reagents, including phosphorylated protein/peptides, antibodies against the phosphospecific amino acid, are important tools to explore the activation of serine, threonine or tyrosine containing proteins. An aberrant protein phosphorylation is a hallmark of human disease, and the enzymes, particularly protein kinases, which control protein phosphorylation are recognized as a major new drug target family.
Western blot - Phosphoserine antibody [PSR-45] (ab6639)
![Western blot - Phosphoserine antibody [PSR-45] (ab6639)](/ps/datasheet/Images/6/ab6639/ab6639_1.jpg)
Anti-Phosphoserine antibody [PSR-45] (ab6639) at 1/200 dilution + Drosophila melanogaster whole tissue lysate 40 ug per lane at 40 µg
Secondary
Sheep anti mouse (HRP) at 1/2000 dilution
Performed under reducing conditions.
This image is an edited version of an image submitted courtesy of an Abreview submitted on 17 August 2005. We do not have any further information relating to this image.
Immunoprecipitation - Anti-Phosphoserine antibody [PSR-45] (ab6639)
![Immunoprecipitation - Anti-Phosphoserine antibody [PSR-45] (ab6639)](/ps/datasheet/images/6/ab6639/Phosphoserine-Primary-antibodies-ab6639-6.jpg)
ab6639 used in Immunoprecipitation.Whole cell lysate prepared from murine mammary cells was loaded at 250µg.Cells were treated with 5ng/ml TGF beta for varying time periods.Protein A was used for the Immunoprecipitation step.ab6639 used at a 1/2000 dilution for 10 hours at 4°C.Western blot was performed with an HRP anti-PCBP1 polyclonal antibody, 1/10000 dilution.
Image courtesy of an anonymous Abreview.
This product has been referenced in:
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![Western blot - Phosphoserine antibody [PSR-45] (ab6639)](/ps/datasheet/Images/6/ab6639/ab6639_1.jpg)
Anti-Phosphoserine antibody [PSR-45] (ab6639) at 1/200 dilution + Drosophila melanogaster whole tissue lysate 40 ug per lane at 40 µg
Secondary
Sheep anti mouse (HRP) at 1/2000 dilution
Performed under reducing conditions.
This image is an edited version of an image submitted courtesy of an Abreview submitted on 17 August 2005. We do not have any further information relating to this image.
![Immunoprecipitation - Anti-Phosphoserine antibody [PSR-45] (ab6639)](/ps/datasheet/images/6/ab6639/Phosphoserine-Primary-antibodies-ab6639-6.jpg)
ab6639 used in Immunoprecipitation.Whole cell lysate prepared from murine mammary cells was loaded at 250µg.Cells were treated with 5ng/ml TGF beta for varying time periods.Protein A was used for the Immunoprecipitation step.ab6639 used at a 1/2000 dilution for 10 hours at 4°C.Western blot was performed with an HRP anti-PCBP1 polyclonal antibody, 1/10000 dilution.
Image courtesy of an anonymous Abreview.
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