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Western blot analysis of Phosphoserine expression in Jurkat (A), mouse brain (B), rat brain (C) whole cell lysates.
Immunohistochemical analysis of Phosphotyrosine staining in human lung cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Product Name:	Anti-Phosphoserine Antibody
Cat No:	CPA9207
Source:	Mouse
Reactivity:	All
Applications:	WB, IH
*Application Key:
H - Human, M - Mouse, R - Rat, B - Bovine, C - Chicken, D - Dog, G - Goat, Mk - Monkey, P - Pig, Rb - Rabbit, S - Sheep, Z - Zebrafish
*Species Reactivity Key:
E- ELISA, WB - Western blot, IH - Immunohistochemistry, IF - Immunofluorescence, FC - Flow cytometry, IC - Immunocytochemistry, IP - Immunoprecipitation, ChIP - Chromatin Immunoprecipitation, EMSA - Electrophoretic Mobility Shift Assay, BL - Blocking, SE - Sandwich ELISA, CBE - Cell-based ELISA, RNAi - RNA interference

Size

Price(USD)

200 μl

350

100 μl

220

30 μl

110

50 μl

150

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Datasheet

MSDS

Description：Mouse monoclonal antibody to Phosphoserine

Immunogen：Purified protein corresponding to Phosphoserine.

Purification：Affinity chromatography

Clonality：Monoclonal

Form：Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.

Dilution：WB (1/1000 - 1/2000), IH (1/50 - 1/200)

Storage/Stability：Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.

Western blot analysis of Phosphoserine expression in Jurkat (A), mouse brain (B), rat brain (C) whole cell lysates.
Immunohistochemical analysis of Phosphotyrosine staining in human lung cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

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