Mouse Monoclonal PPM1A antibody. Suitable for ELISA, WB, IHC-P, ICC/IF and reacts with Mouse, Human samples. Cited in 20 publications. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human PPM1A.
查看别名
PPPM1A, PPM1A, Protein phosphatase 1A, Protein phosphatase 2C isoform alpha, Protein phosphatase IA, PP2C-alpha
- WB
AbReview4237****
Western blot - Anti-PPM1A antibody [p6c7] (AB14824)
This image is courtesy of an Abreview submitted by Xia Lin on 2 March 2006.
This image was generated using the ascites version of the product.
All lanes:
Western blot - Anti-PPM1A antibody [p6c7] (ab14824) at 1/1000 dilution
All lanes:
HeLa whole cell lysate
Secondary
All lanes:
HRP conjugated anti-mouse antibody
Predicted band size: 42 kDa
Observed band size: 45 kDa
true
Exposure time: 10s
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PPM1A antibody [p6c7] (AB14824)
ab14824 staining human colon. Staining is localised to cytoplasm.
Left panel : with primary antibody at 4ug/ml. Right panel : isotype control.
Sections were stained using an automated system DAKO Autostainer Plus , at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 antigen retrieval buffer EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
This image was generated using the ascites version of the product.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-PPM1A antibody [p6c7] (AB14824)
Immunocytochemistry/ Immunofluorescence analysis of PP2C alpha/PPM1A in HeLa cells. The cell was stained with ab14824 (1 : 100). The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue).
- WB
Supplier Data
Western blot - Anti-PPM1A antibody [p6c7] (AB14824)
All lanes:
Western blot - Anti-PPM1A antibody [p6c7] (ab14824) at 1/1000 dilution
Lane 1:
Jurkat cell lysate at 40 µg
Lane 2:
HeLa cell lysate at 40 µg
Lane 3:
K-562 cell lysate at 40 µg
Lane 4:
MCF7 cell lysate at 40 µg
Lane 5:
A549 cell lysate at 40 µg
Lane 6:
Raji cell lysate at 40 µg
Lane 7:
Mouse kidney tissue lysate at 40 µg
Lane 8:
Mouse brain tissue lysate at 40 µg
Lane 9:
Mouse liver tissue lysate at 40 µg
Secondary
All lanes:
goat anti-mouse secondary antibody conjugated to HRP
Predicted band size: 42 kDa
false
- WB
Unknown
Western blot - Anti-PPM1A antibody [p6c7] (AB14824)
Western blot analysis of mouse liver cytosol extract using ab14824 at a dilution of 1/250. Proteins were visualised using a goat anti-mouse secondary antibody conjugated to HRP and a DAB detection system. Western blot analysis of mouse liver cytosol extract using ab14824 at a dilution of 1/250. Proteins were visualised using a goat anti-mouse secondary antibody conjugated to HRP and a DAB detection system.
This image was generated using the ascites version of the product.
All lanes:
Western blot - Anti-PPM1A antibody [p6c7] (ab14824)
Predicted band size: 42 kDa
false
- WB
Lab
Western blot - Anti-PPM1A antibody [p6c7] (AB14824)
Lane 1 : Wild-type HAP1 cell lysate (20 μg)
Lane 2 : PPM1A knockout HAP1 cell lysate (20 μg)
Lane 3 : HeLa cell lysate (20 μg)
Lane 4 : Jurkat cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab14824 observed at 42 kDa. Red - loading control, ab18251, observed at 52 kDa.
ab14824 was shown to specifically react with PPM1A when PPM1A knockout samples were used. Wild-type and PPM1A knockout samples were subjected to SDS-PAGE. ab14824 diluted to 1/250 and ab18251 (loading control to alpha Tubulin) diluted to 1/10000 were incubated overnight at 4°C. Blots were developed with Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (ab216772) and Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (ab216777) secondary antibodies at 1/10000 dilution for 1 hour at room temperature before imaging.
This image was generated using the ascites version of the product.
All lanes:
Western blot - Anti-PPM1A antibody [p6c7] (ab14824)
Predicted band size: 42 kDa
false
- WB
Lab
Western blot - Anti-PPM1A antibody [p6c7] (AB14824)
Lanes 1-4 : Merged signal (red and green). Green - ab14824 observed at 42 kDa. Red - loading control ab181602 observed at 36 kDa.
ab14824 Anti-PPM1A antibody [p6c7] was shown to specifically react with PPM1A in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab265348 (knockout cell lysate ab259055) was used. Wild-type and PPM1A knockout samples were subjected to SDS-PAGE. ab14824 and Anti-GAPDH antibody[EPR16891] - Loading Control (ab181602) were incubated overnight at 4°C at 1 in 500 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (ab216777) and Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (ab216772) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-PPM1A antibody [p6c7] (ab14824) at 1/500 dilution
Lane 1:
Wild-type HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
PPM1A knockout HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
Western blot - Human PPM1A knockout HeLa cell line (<a href='/products/cell-lines/human-ppm1a-knockout-hela-cell-line-ab265348'>ab265348</a>)
Lane 3:
HAP1 whole cell lyate at 20 µg
Lane 4:
Jurkat (Human T cell leukemia cell line from peripheral blood) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-680rd-preadsorbed-ab216777'>ab216777</a>) at 1/10000 dilution
Predicted band size: 41 kDa,42 kDa
Observed band size: 42 kDa
false
反应性数据
产品详情
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
PPM1A regulates many cellular mechanisms by dephosphorylating targets and acting as a negative regulator of several signaling pathways. It modulates stress responses cell cycle progression and immune responses. PPM1A does not typically form complexes with other proteins but interacts closely with specific signaling molecules to control their activity. This regulation influences cellular homeostasis and growth in response to external and internal signals.
Pathways
PPM1A influences the TGF-beta signaling pathway where it interacts with and deactivates SMAD proteins by dephosphorylation. It also participates in the p38 MAPK pathway. These interactions highlight its role in controlling transduction signals initiated by growth factors and stress. By regulating these pathways PPM1A maintains a balance in cellular responses to growth and environmental stresses.
产品实验方案
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靶点信息
文献 (20)
Recent publications for all applications. Explore the full list and refine your search
Phytotherapy research : PTR 37:4771-4790 PubMed37434441
2023
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JCI insight 8: PubMed36752205
2023
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Cell reports 41:111862 PubMed36543129
2022
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Science advances 8:eabq2423 PubMed36179025
2022
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Disease markers 2021:2217663 PubMed34336002
2021
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Allergy, asthma & immunology research 12:859-876 PubMed32638565
2020
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Experimental and therapeutic medicine 20:926-932 PubMed32742335
2020
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EBioMedicine 42:458-469 PubMed30926424
2019
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Cell reports 23:1124-1137 PubMed29694890
2018
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Nature cell biology 17:434-44 PubMed25751141
2015
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