Anti-c-Jun (phospho S63) antibody [Y172]
- 20ul selling size
- RabMAb
- Recombinant
- What is this?
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
View Alternative Names
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='/en-us/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='/en-us/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='/en-us/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.
Related conjugates and formulations (7)
-
Anti-c-Jun (phospho S63) antibody [Y172] - BSA and Azide free
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-c-Jun (phospho S63) antibody [Y172]
-
603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-c-Jun (phospho S63) antibody [Y172]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-c-Jun (phospho S63) antibody [Y172]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-c-Jun (phospho S63) antibody [Y172]
-
565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-c-Jun (phospho S63) antibody [Y172]
-
775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-c-Jun (phospho S63) antibody [Y172]
Reactivity data
Product details
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.
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
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.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (116)
Recent publications for all applications. Explore the full list and refine your search
Nature 644:516-526 PubMed40681898
2025
Applications
Unspecified application
Species
Unspecified reactive species
Cell reports. Medicine 6:102000 PubMed40056904
2025
Applications
Unspecified application
Species
Unspecified reactive species
Frontiers in immunology 16:1515605 PubMed39963142
2025
Applications
Unspecified application
Species
Unspecified reactive species
Cellular and molecular life sciences : CMLS 82:45 PubMed39833479
2025
Applications
Unspecified application
Species
Unspecified reactive species
Journal of cellular and molecular medicine 28:e70237 PubMed39643939
2024
Applications
Unspecified application
Species
Unspecified reactive species
The Journal of physiology 602:4959-4985 PubMed39197117
2024
Applications
Unspecified application
Species
Unspecified reactive species
Signal transduction and targeted therapy 9:214 PubMed39117631
2024
Applications
Unspecified application
Species
Unspecified reactive species
iScience 27:110286 PubMed39055952
2024
Applications
Unspecified application
Species
Unspecified reactive species
Military Medical Research 11:41 PubMed38937853
2024
Applications
Unspecified application
Species
Unspecified reactive species
iScience 27:109502 PubMed38591009
2024
Applications
Unspecified application
Species
Unspecified reactive species
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