Anti-c-Jun (phospho S63) 抗体 [Y172]
Anti-c-Jun (phospho S63) antibody [Y172]
- 20ul selling size
- RabMAb
- Recombinant
- 了解详情
5
(4 Reviews)
|
(116 Publications)
Anti-c-Jun (phospho S63) antibody [Y172] (ab32385) is a rabbit monoclonal antibody detecting c-Jun in Western Blot, IHC-P, ICC/IF, ELISA, Dot Blot. Suitable for Human, Mouse.
- Biophysical QC for unrivalled batch-batch consistency
- Over 90 publications
- Trusted since 2006
查看别名
Transcription factor Jun, Activator protein 1, Proto-oncogene c-Jun, Transcription factor AP-1 subunit Jun, V-jun avian sarcoma virus 17 oncogene homolog, p39, AP1, JUN
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized A431 (Human epidermoid carcinoma cell line) cells labeling c-Jun (phospho S63) with ab32385 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing the expression was increased after treatment with anisomycin (1 μg/ml for 15 minutes), then decreased after treatment with the Lambda Protein Phosphatase treatment 31℃ for 2 hours. The nuclear counter stain is DAPI (blue).
Counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at a 1/200 dilution (red).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human breast tissue sections labeling c-Jun with Purified ab32385 at 1 : 250 dilution (0.46 µg/ml). Heat mediated antigen retrieval was performed using using ab93684 (Tris/EDTA buffer, pH 9.0)ImmunoHistoProbe one step HRP Polymer (ready to use)was used as the secondary antibody.Negative control : PBS instead of the primary antibody.Hematoxylinwas used as a counterstain
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Paraffin-embedded human breast carcinoma tissue stained for c-Jun (phospho S63) with unpurified ab32385 at a 1/50 dilution in immunohistochemical analysis.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Immunocytochemistry confocal image of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized anisomycin-treated NIH/3T3 cell line (mouse embryonic fibroblast), staining nuclear c-Jun with ab32385 at 1 : 500 dilution and ab150077 AlexaFluor®488 Goat anti-Rabbit secondary at 1 : 1000 dilution. The counterstain was ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at 1 : 200 dilution, and the nuclear counterstain was DAPI (blue).
The NIH/3T3 cells were treated with 250 ng/ml Anisomycin for 30 minutes and then the signal decreased after phosphatase treatment at 37°C for 2 hours.
- WB
Lab
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (ab32385) at 1/1000 dilution
Lane 1:
HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 15 µg
Lane 2:
HeLa (Human cervix adenocarcinoma epithelial cell) treated with 1ug/mL anisomycin for 15 minutes whole cell lysates at 15 µg
Lane 3:
HeLa (Human cervix adenocarcinoma epithelial cell) treated with 1ug/ml anisomycin for 15 minutes whole cell lysates. Then the membrane was incubated with phosphatase. at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 35 kDa
false
- WB
Unknown
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Blocking and diluting buffer : 5% NFDM/TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32385).
All lanes:
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (ab32385) at 0.1 µg/mL
Lane 1:
HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 15 µg
Lane 2:
HeLa (Human cervix adenocarcinoma epithelial cell) treated with 1 ug/ml anisomycin for 15 minutes whole cell lysates at 15 µg
Lane 3:
HeLa (Human cervix adenocarcinoma epithelial cell) treated with 1 ug/ml anisomycin for 15 minutes whole cell lysates 15ug. Then the membrane was incubated with phosphatase. at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 35 kDa
false
- Dot
Unknown
Dot Blot - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Unpurified ab32385 used at a 1 : 1000 dilution.
Secondary antibody is Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) used at a 1 : 100,000 dilution. Blocking/Diluting buffer and concentration : 5% NFDM/TBST.
Lane 1 : Human c-Jun (pS63) phospho peptide.
Lane 2 : Human c-Jun non-phospho peptide.
Exposure time 3 minutes.
- WB
Unknown
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
All lanes:
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (ab32385) at 1/10000 dilution
Lanes 1 and 3:
Untreated NIH/3T3 (Mouse embyro fibroblast cell line) cell lysate
Lane 2:
NIH/3T3 (Mouse embyro fibroblast cell line) cell lysate treated with ultraviolet light
Lane 4:
NIH/3T3 (Mouse embyro fibroblast cell line) cell lysate treated with 25 µg/ml Anisomycin for 15 minutes at 37°C
Predicted band size: 35 kDa
Observed band size: 42 kDa
false
- WB
Unknown
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Blocking and diluting buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-c-Jun (phospho S63) antibody [Y172] (ab32385) at 0.1 µg/mL
Lane 1:
NIH/3T3 (Mouse embryonic fibroblast) whole cell lysates at 15 µg
Lane 2:
NIH/3T3 (Mouse embryonic fibroblast) treated with 250 ng/ml anisomycin for 30 minutes whole cell lysates at 15 µg
Lane 3:
NIH/3T3 (Mouse embryonic fibroblast) treated with 250 ng/ml anisomycin for 30 minutes whole cell lysates. Then the membrane was incubated with phosphatase at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 35 kDa
false
- ELISA
Unknown
ELISA - Anti-c-Jun (phospho S63) antibody [Y172] (AB32385)
Antigen pS63 : c-Jun (phospho S63); NP : c-Jun non-phospho. Antigen concentration 0.01~1 ng/ml.
Primary antibody concentration range 0~1000 ng/ml.
Secondary antibody is an Alkaline Phosphatase-conjugated Goat Anti-Rabbit IgG(H+L) used at a 1 : 2500 dilution.
不同偶联物与剂型 (7)
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-c-Jun (phospho S63) antibody [Y172]
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-c-Jun (phospho S63) antibody [Y172]
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Anti-c-Jun (phospho S63) antibody [Y172] - BSA and Azide free
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-c-Jun (phospho S63) antibody [Y172]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-c-Jun (phospho S63) antibody [Y172]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-c-Jun (phospho S63) antibody [Y172]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-c-Jun (phospho S63) antibody [Y172]
反应性数据
产品详情
What is this antibody validated in?
Anti-c-Jun (phospho S63) antibody [Y172] (ab32385) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Immunohistochemistry (IHC-P), Immunocytochemistry/immunofluorescence (ICC/IF), ELISA, Dot Blot in Human, Mouse samples.
What is the molecular weight of c-Jun?
Anti-c-Jun (phospho S63) [Y172] (ab32385) specifically detects a band for c-Jun (UniProt: P05412) at a molecular weight of 36kDa.
Trusted by the scientific community
Anti-c-Jun (phospho S63) [Y172] (ab32385) was first used in a scientific publication in 2006 and has been cited over 90 times in peer-reviewed journals.
Trial sizes available!
Test your antibody or perform pre-screening before committing to a larger quantity. Sold in 10µl. Discover our selection of trial-size antibodies.
Other related products
We have a range of other formats of antibody clone [Y172] also available for your convenience: ab32385, Carrier free - ab227533, Alexa Fluor® 488 - ab310948, Alexa Fluor® 647 - ab311066, Alexa Fluor® 594 - ab311651, Alexa Fluor® 568 - ab312924, Alexa Fluor® 555 - ab313136, Alexa Fluor® 750 - ab321597
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.
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
C-Jun impacts cellular activities by being a significant part of the AP-1 transcription factor complex interacting with other proteins such as Fos. This interaction allows c-Jun to modulate gene expression in response to cellular stimuli. In particular c-Jun influences cell cycle progression and differentiation. Therefore its activity is necessary for physiological and pathological processes. As c-jun's function remains tightly regulated any changes can have wide-ranging effects.
Pathways
C-Jun significantly influences the MAPK/ERK and JNK pathways. These pathways play important roles in cellular responses to stress growth factors and cytokines. Within these pathways c-Jun interacts with proteins such as JNK which phosphorylates c-Jun and enhances its activity. These interactions allow c-Jun to regulate target genes involved in important cellular processes without much delay. Understanding c-Jun's function in these pathways helps elucidate how cells control division survival and apoptosis.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
文献 (116)
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