Anti-Phosphoserine antibody [EPR28666-51]
- BOND RX™ Validated
- Recombinant
- RabMAb
- 20ul selling size
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Rabbit Recombinant Monoclonal Phosphoserine antibody. Suitable for Dot, I-ELISA, IHC-P, WB and reacts with Synthetic peptide, Human, Mouse samples.
View Alternative Names
PS, pSER, phospho-Ser
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Phosphoserine antibody [EPR28666-51] (AB322140)
Immunohistochemical analysis of paraffin-embedded (A) HeLa (human cervix adenocarcinoma epithelial cell) without alkaline phosphatase treatment cell pellet; (B) HeLa+Calyculin A(100nM 30min) without alkaline phosphatase treatment cell pellet ; (C) HeLa with alkaline phosphatase treatment cell pellet; (D) HeLa +Calyculin A(100nM 30min) with alkaline phosphatase treatment cell pellet tissue labeling Phosphoserine with ab322140 at 1/500 (0.98 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on cell pellets of (A) untreated HeLa (human cervix adenocarcinoma epithelial cell), (B) HeLa+Calyculin A(100nM 30min), no staining on cell pellets of (C) HeLa with alkaline phosphatase treatment and (D) HeLa +Calyculin A(100nM 30min) with alkaline phosphatase treatment. The section was incubated with ab322140 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Phosphoserine antibody [EPR28666-51] (AB322140)
Immunohistochemical analysis of paraffin-embedded (A) Human lung without alkaline phosphatase treatment; (B) Human lung with alkaline phosphatase treatment tissue labeling Phosphoserine with ab322140 at 1/100 (4.9 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on (A) human lung without alkaline phosphatase treatment; negative staining on (B) human lung with alkaline phosphatase treatment. The section was incubated with ab322140 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Phosphoserine antibody [EPR28666-51] (AB322140)
Immunohistochemical analysis of paraffin-embedded (A) Mouse lung without alkaline phosphatase treatment; (B) Mouse lung with alkaline phosphatase treatment tissue labeling Phosphoserine with ab322140 at 1/100 (4.9 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on (A) mouse lung without alkaline phosphatase treatment; negative staining on (B) mouse lung with alkaline phosphatase treatment. The section was incubated with ab322140 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Phosphoserine antibody [EPR28666-51] (AB322140)
Immunohistochemical analysis of paraffin-embedded (A) RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) without alkaline phosphatase treatment cell pellet; (B) RAW 264.7 with alkaline phosphatase treatment cell pellet tissue labeling Phosphoserine with ab322140 at 1/500 (0.98 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on cell pellets of (A) RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) and no staining on cell pellets of (B) RAW 264.7 with alkaline phosphatase treatment. The section was incubated with ab322140 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins.
- WB
Supplier Data
Western blot - Anti-Phosphoserine antibody [EPR28666-51] (AB322140)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
This blot was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.
All lanes:
Western blot - Anti-Phosphoserine antibody [EPR28666-51] (ab322140) at 1/1000 dilution
Lane 1:
Untreated HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 60 µg
Lane 2:
HeLa treated with 100nM calyculin A for 30min) whole cell lysate at 60 µg
Lane 3:
Untreated B16-F0 (mouse melanoma epithelial-like cell) whole cell lysate at 60 µg
Lane 4:
B16-F0 treated with 1uM Okadaic Acid for 60min whole cell lysate at 60 µg
Lane 5:
Untreated Jurkat (human T cell leukemia T lymphocyte from peripheral blood) whole cell lysate at 60 µg
Lane 6:
Jurkat treated with 100nM Calyculin A for 30min whole cell lysate at 60 µg
Lane 7:
Untreated RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 60 µg
Lane 8:
RAW 264.7 treated with 100nM Calyculin A for 30min) whole cell lysate at 60 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 25-300 kDa,36 kDa
true
Exposure time: 70s
- I-ELISA
Supplier Data
Indirect ELISA - Anti-Phosphoserine antibody [EPR28666-51] (AB322140)
Indirect ELISA analysis of ab322140 at 1000-0 ng/ml. The Secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1 : 2500 dilution.
Antigen : Phosphoserine peptide, Phosphothreonine peptide, Phosphotyrosine peptide, Non-phosphoserine peptide.
Antigen concentration : 1000 ng/ml
- Dot
Supplier Data
Dot Blot - Anti-Phosphoserine antibody [EPR28666-51] (AB322140)
Dot blot analysis of Phosphoserine using ab322140 at 1 : 1000 (0.49 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Lane1 : Phosphoserine peptide a
Lane2 : Phosphoserine peptide b
Lane3 : phosphothreonine peptide
Lane4 : phosphotyrosine peptide
Lane5 : Non-phosphoserine peptide
Exposure time : 180 seconds.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Dot Blot - Anti-Phosphoserine antibody [EPR28666-51] (ab322140) at 1/1000 dilution
Lane 1:
Phosphoserine peptide a
Lane 2:
Phosphoserine peptide b
Lane 3:
phosphothreonine peptide
Lane 4:
phosphotyrosine peptide
Lane 5:
Non-phosphoserine peptide
Secondary
All lanes:
Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-Phosphoserine antibody [EPR28666-51] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Phosphorylated serine residues are involved in controlling a multitude of cellular processes including cell cycle regulation and apoptosis. These phosphorylated regions form parts of protein kinases phosphatases and glycoproteins acting as switches for cellular signaling. Phosphoserine is often part of multi-protein complexes binding to other proteins and influencing their activity through changes in conformation. This active participation in biological pathways signifies its significant influence in maintaining cellular homeostasis.
Pathways
Phosphoserine plays a significant role in the MAPK signaling and PI3K/AKT pathways both important for cell growth and survival. It interacts with proteins like AKT and MAPK facilitating cellular responses to extracellular stimuli. This phosphorylation state dictates the activation or inactivation of these proteins effectively regulating key steps in signal transduction and transcriptional control. Such pathways highlight the importance of phosphoserine in coordinating complex cellular activities.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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