Anti-ERK1 + ERK2 抗体 [ERK-7D8]
Anti-ERK1 + ERK2 antibody [ERK-7D8]
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5
(2 Reviews)
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(136 Publications)
Mouse Monoclonal ERK1 antibody. Suitable for IHC-P, ICC/IF and reacts with Mouse, Human samples. Cited in 136 publications. Immunogen corresponding to Synthetic Peptide within Rat Mapk3 aa 300-350.
查看别名
ERK1, PRKM3, MAPK3, Mitogen-activated protein kinase 3, MAP kinase 3, MAPK 3, ERT2, Extracellular signal-regulated kinase 1, Insulin-stimulated MAP2 kinase, MAP kinase isoform p44, Microtubule-associated protein 2 kinase, p44-ERK1, ERK-1, p44-MAPK
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ERK1 + ERK2 antibody [ERK-7D8] (AB54230)
Immunocytochemistry/ Immunofluorescence analysis of ERK1 + ERK2 Antibody (ab54230) was done on 70% confluent log phase U87-MG cells. The cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilized with 0.25% Triton™ X-100 for 10 minutes, and blocked with 5% BSA for 1 hour at room temperature. The cells were labeled with ERK1 + ERK2 Antibody [ERK-7D8] (ab54230) at 1μg/mL in 1% BSA and incubated for 3 hours at room temperature and then labeled with Alexa Flour 488® Rabbit Anti-Mouse IgG Secondary Antibody at a dilution of 1/400 for 45 minutes at room temperature (Panel a : green). Nuclei (Panel b : blue) were stained with DAPI. F-actin (Panel c : red) was stained with Alexa Fluor 594® Phalloidin. Panel d is a merged image showing cytoplasmic and nuclear localization. Panel e is a no primary antibody control. The images were captured at 40X magnification.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ERK1 + ERK2 antibody [ERK-7D8] (AB54230)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast carcinoma tissue labeling ERK1 + ERK2 with ab54230. Staining in the cytoplasm and nucleus (right), compared to a negative control without primary antibody (left). To expose target proteins, antigen retrieval was performed using 10mM sodium citrate (pH 6.0), microwaved for 8-15 min. Following antigen retrieval, tissues were blocked in 3% H2O2-methanol for 15 min at room temperature, washed with ddH2O and PBS, and then probed with a ERK1/2 monoclonal antibody (ab54230) diluted in 3% BSA-PBS at a dilution of 1/50 overnight at 4°C in a humidified chamber. Tissues were washed extensively in PBST and detection was performed using an HRP-conjugated secondary antibody followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ERK1 + ERK2 antibody [ERK-7D8] (AB54230)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human cortex tissue labeling ERK1 + ERK2 with ab54230.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ERK1 + ERK2 antibody [ERK-7D8] (AB54230)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of mouse stomach tissue labeling ERK1 + ERK2 with ab54230. Staining in the cytoplasm and nucleus (right) compared to a negative control without primary antibody (left). To expose target proteins, antigen retrieval was performed using 10mM sodium citrate (pH 6.0), microwaved for 8-15 min. Following antigen retrieval, tissues were blocked in 3% H2O2 -methanol for 15 min at room temperature, washed with ddH2O and PBS, and then probed with a ERK1/2 monoclonal antibody (ab54230) diluted in 3% BSA-PBS at a dilution of 1/20 overnight at 4°C in a humidified chamber. Tissues were washed extensively in PBST and detection was performed using an HRP-conjugated secondary antibody followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.
反应性数据
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存时间
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
ERK1 and ERK2 play key roles in cell proliferation differentiation and survival. They form part of a cascade that includes upstream activators such as MEK1/2 and downstream targets including transcription factors. As components of the MAPK signaling complex ERK1/2 regulate gene expression through phosphorylation events impacting cellular responses to various stimuli. Their activation often hinges on growth factors cytokines and stress signals facilitating cellular adaptation to environmental changes.
Pathways
Regarding pathways ERK1/2 sit within the MAPK/ERK pathway and are significant in the Ras/Raf/MEK/ERK cascade one of the foremost signaling mechanisms in cells. They interact with several proteins including Ras and Raf which modulate their activation. This pathway is important for transmitting signals from the cell surface to the DNA in the cell nucleus impacting gene regulation and cell fate decisions. ERK1/2 proteins therefore serve as critical nodes linking extracellular signals to cellular responses ensuring balanced cell function.
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靶点信息
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文献 (136)
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American journal of cancer research 15:2353-2374 PubMed40520857
2025
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Scientific reports 15:12914 PubMed40234489
2025
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Asian Pacific journal of cancer prevention : APJCP 25:2193-2201 PubMed38918683
2024
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Cell death and differentiation 31:804-819 PubMed38698060
2024
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Cell death discovery 9:406 PubMed37919290
2023
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Acta biochimica et biophysica Sinica 55:449-459 PubMed36942990
2023
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Journal of functional biomaterials 14: PubMed36976051
2023
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Annals of translational medicine 10:1392 PubMed36660714
2023
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Advanced healthcare materials 12:e2202275 PubMed36625629
2023
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EMBO molecular medicine 15:e16244 PubMed36533294
2022
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