Anti-PPP1CA + PPP1CB antibody [EP1511Y]
- RabMAb
- Recombinant
- What is this?
1
(1 Review)
|
(11 Publications)
Rabbit Recombinant Monoclonal PPP1CB antibody. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Human, Mouse, Rat samples. Cited in 11 publications.
View Alternative Names
Serine/threonine-protein phosphatase PP1-beta catalytic subunit, PP-1B, PPP1CD, PPP1CB
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
Overlay histogram showingHeLa cells stained with ab52619 (red line) at 1/150 dilution. The cells were fixed with 80% methanol. The secondary antibody used was a FITC conjugated goat anti-rabbit IgG at 1/150 dilution. Isotype control antibody (black line) was rabbit monoclonal IgG used under the same conditions. Cells also incubated without primary antibody and secondary antibody (blue line)
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
ab52619 staining PP1CA + 1CB in Human cerebrum cortex tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed and paraffin-embedded, antigen retrieval was by heat mediation in Tris/EDTA buffer pH9. Samples were incubated with primary antibody (1/50). An undiluted HRP-conjugated mouse anti-rabbit IgG was used as the secondary antibody. Tissue counterstained with Hematoxylin. PBS was used in the negative control rather than the Primary antibody.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
ab52619 staining PPP1CA + 1CB in the HepG2 cell line by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with 4% Paraformaldehyde permeabilized with 0.1% Triton X-100. Samples were incubated with primary antibody (1/50). ab150077(1/500) an Alexa Fluor®488-conjugated Goat anti-rabbit IgG was used as the secondary antibody. Nuclei were counterstained with DAPI.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
Overlay histogram showing HeLa cells stained with ab52619, unpurified (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab52619, 1/100 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
- IP
Unknown
Immunoprecipitation - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
ab52619 (purified) at 1/30 immunoprecipitating PPP1CA + 1CB in Jurkat cell lysate. For western blotting, a HRP-conjugated Goat anti-rabbit IgG, specific to the non-reduced form of IgG was used as the secondary antibody (1/1000).
Blocking buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM /TBST.
All lanes:
Immunoprecipitation - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (ab52619)
Predicted band size: 37 kDa
false
- WB
Supplier Data
Western blot - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
All lanes:
Western blot - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (ab52619) at 1/20000 dilution
Lane 1:
SKBR-3 cell lysate at 20 µg
Lane 2:
Jurkat cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), HRP-conjugated at 1/1000 dilution
Predicted band size: 37 kDa
false
- WB
Supplier Data
Western blot - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
All lanes:
Western blot - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (ab52619) at 1/100000 dilution
Lane 1:
Mouse Brain lysate at 20 µg
Lane 2:
Rat Brain lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), HRP-conjugated at 1/1000 dilution
Predicted band size: 37 kDa
false
- WB
Supplier Data
Western blot - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (AB52619)
All lanes:
Western blot - Anti-PPP1CA + PPP1CB antibody [EP1511Y] (ab52619) at 1/100000 dilution
Lane 1:
T47-D cell Lysate at 20 µg
Lane 2:
HeLa cell Lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), HRP-conjugated at 1/1000 dilution
Predicted band size: 37 kDa
false
Related conjugates and formulations (2)
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Anti-PPP1CA + PPP1CB antibody [EP1511Y] - BSA and Azide free
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HRP Anti-PPP1CA + PPP1CB antibody [EP1511Y]
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 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
Protein phosphatase 1 catalytic subunits like PPP1CA and PPP1CB regulate important processes such as cell division and glycogen metabolism. These subunits typically are part of larger multiprotein complexes allowing for specific substrate targeting. By dephosphorylating specific proteins they act as regulatory signals within cellular systems influencing numerous biochemical pathways and responses. In neuronal tissues for example these phosphatases impact learning and memory by regulating synaptic plasticity through dephosphorylation cycles.
Pathways
These phosphatase subunits engage in the MAP kinase and PI3K-Akt signaling pathways. In the MAP kinase pathway they interact with proteins such as ERK helping regulate cell proliferation and differentiation. In the PI3K-Akt pathway they modulate the activity of key components influencing processes like cell survival and growth. The regulatory function of PPP1CA and PPP1CB within these pathways facilitates critical cellular responses to various extracellular signals thereby affecting the overall cellular physiology.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (11)
Recent publications for all applications. Explore the full list and refine your search
Scientific reports 13:13927 PubMed37626185
2023
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Redox biology 64:102780 PubMed37354826
2023
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Experimental and therapeutic medicine 25:154 PubMed36911368
2023
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EMBO reports 22:e52645 PubMed34342389
2021
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Cell death and differentiation 27:2158-2175 PubMed31969690
2020
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Cells 8: PubMed31387295
2019
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Frontiers in cellular neuroscience 13:179 PubMed31118889
2019
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Molecular and cellular endocrinology 450:74-82 PubMed28454724
2017
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The Journal of neuroscience : the official journal of the Society for Neuroscience 33:15879-93 PubMed24089494
2013
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WB
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The Journal of experimental medicine 209:679-96 PubMed22430491
2012
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com