P3430
Monoclonal Anti-Phosphoserine antibody produced in mouse
clone PSR-45, ascites fluid
Synonyme(s) :
Monoclonal Anti-Phosphoserine, Phospho Ser, Phospho serine, Phospho−Ser, Phospho−serine
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A propos de cet article
NACRES:
NA.44
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
PSR-45, monoclonal
Application:
ELISA (i), WB
Citations:
56
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Laissez-nous vous aiderbiological source
mouse
conjugate
unconjugated
antibody form
ascites fluid
antibody product type
primary antibodies
clone
PSR-45, monoclonal
contains
15 mM sodium azide
technique(s)
indirect ELISA: 1:4,000, western blot: 1:500-1:1,000
isotype
IgG1
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
General description
Monoclonal Anti-Phosphoserine (mouse IgG1 isotype) is derived from the hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse.
Immunogen
phosphoserine conjugated to Keyhole Limpet Hemocyanin (KLH).
Application
Anti-Phosphoserine antibody may be used for indirect ELISA at a working dilution of 1:4000. For immunoblotting using rat brain cortex extracts, a working dilution of 1:500-1:1100 may be used. The antibody was used for immunoblotting to detect proteins phosphorylated at serine in stem extracts of Arabidopsis thalliana at a working dilution of 1:250.
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Western Blotting (1 paper)
Western blotting following immunoprecipitation (1 paper)
Western Blotting (1 paper)
Western blotting following immunoprecipitation (1 paper)
Monoclonal Anti-Phosphoserine antibody produced in mouse has been used in western blotting.
Biochem/physiol Actions
By ELISA and dot blot, the antibody reacts specifically with phosphorylated serine, both as free amino acid or conjugated to carriers such as BSA or KLH. No cross-reactivity is observed with non-phosphorylated serine, phosphothreonine, phosphotyrosine, AMP or ATP. This antibody has been used in immunoblotting for the localization of some phosphoserine-containing proteins. Certain proteins known to contain phosphorylated serine may not be recognized by this antibody due to steric hindrance of the recognition site.
Phosphoserine (PS) can be used as a template to detect cancer antigen 125 (CA 125).
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.
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Classe de stockage
12 - Non Combustible Liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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Sapan J Patel et al.
Journal of cellular and molecular medicine, 21(3), 456-466 (2016-09-30)
B-cell novel protein-1 (BCNP1) or Family member of 129C (FAM129C) was identified as a B-cell-specific plasma-membrane protein. Bioinformatics analysis predicted that BCNP1 might be heavily phosphorylated. The BCNP1 protein contains a pleckstrin homology (PH) domain, two proline-rich (PR) regions and
Vinculin but not alpha-actinin is a target of PKC phosphorylation during junctional assembly induced by calcium
Perez-MM, et al.
Journal of Cell Science, 111(23), 3563-3571 (1998)
Identification of cellulose synthase AtCesA7 (IRX3) in vivo phosphorylation sites?a potential role in regulating protein degradation
Taylor NG
Plant Molecular Biology, 64(1-2), 161-171 (2007)
Pierrick Dudognon et al.
FEBS letters, 561(1-3), 44-50 (2004-03-12)
Endoplasmic reticulum (ER)-to-Golgi transport is blocked in mammalian cells during mitosis; however, the mechanism underlying this blockade remains unknown. Since COPII proteins are involved in this transport pathway, we investigated at the biochemical level post-translational modifications of COPII components during
Neil G Taylor
Plant molecular biology, 64(1-2), 161-171 (2007-04-12)
Cellulose is central to plant development and is synthesised at the plasma membrane by an organised protein complex that contains three different cellulose synthase proteins. The ordered assembly of these three catalytic subunits is essential for normal cellulose synthesis. The
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