Recombinant Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)
![Immunocytochemistry/ Immunofluorescence - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-234725-IF.jpg "Immunocytochemistry/ Immunofluorescence - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)")
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR16797-211] to JNK1+JNK2+JNK3
- Suitable for: Flow Cyt, WB, IP, ICC/IF
- Reacts with: Mouse, Rat, Chicken, Cow, Dog, Human, Zebrafish, African green monkey, Xenopus tropicalis, Recombinant fragment
Overview
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Product name
Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211]
See all JNK1+JNK2+JNK3 primary antibodies -
Description
Rabbit monoclonal [EPR16797-211] to JNK1+JNK2+JNK3 -
Host species
Rabbit -
Tested Applications & Species
See all applications and species dataApplication Species Flow Cyt HumanICC/IF MouseHumanIP HumanWB MouseRatHumanZebrafishRecombinant fragment
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Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: Human JNK1, JNK2 and JNK3 full length recombinant proteins; K562, HeLa, Jurkat, Neuro-2a, UMNSAH/DF-1, MDCK, MDBK and COS-1 whole cell lysates; Zebrafish and X. tropicalis lysates. Mouse brain, Rat brain, Rat heart, RAW 264.7, PC-12 and NIH/3T3 lysates. ICC/IF: HeLa cells. IP: Jurkat whole cell extract. Flow Cyt: HeLa cells
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General notes
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing the problem with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation.
One factor contributing to the crisis is the use of antibodies that are not suitable. This can lead to misleading results and the use of incorrect data informing project assumptions and direction. To help address this challenge, we have introduced an application and species grid on our primary antibody datasheets to make it easy to simplify identification of the right antibody for your needs.
Learn more here.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. -
Storage buffer
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol, 0.05% BSA -
Concentration information loading... -
Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR16797-211 -
Isotype
IgG -
Research areas
Associated products
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Alternative Versions
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Compatible Secondaries
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Conjugation kits
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Isotype control
Applications
The Abpromise guarantee
Our Abpromise guarantee covers the use of ab179461 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Tested applications are guaranteed to work and covered by our Abpromise guarantee.
Predicted to work for this combination of applications and species but not guaranteed.
Does not work for this combination of applications and species.
| Application | Species |
|---|---|
| Flow Cyt |
Human
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| ICC/IF |
Mouse
Human
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| IP |
Human
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| WB |
Mouse
Rat
Human
Zebrafish
Recombinant fragment
|
| All applications |
Monkey
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| Application | Abreviews | Notes |
|---|---|---|
| Flow Cyt |
1/180.
ab172730 - Rabbit monoclonal IgG, is suitable for use as an isotype control with this antibody.
|
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| WB | (4) |
1/1000. Detects a band of approximately 54, 46 kDa (predicted molecular weight: 48 kDa).
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| IP |
1/50.
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| ICC/IF | (3) |
1/250.
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| Notes |
|---|
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Flow Cyt
1/180. ab172730 - Rabbit monoclonal IgG, is suitable for use as an isotype control with this antibody.
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WB
1/1000. Detects a band of approximately 54, 46 kDa (predicted molecular weight: 48 kDa). |
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IP
1/50. |
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ICC/IF
1/250. |
Target
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Function
Serine/threonine-protein kinase involved in various processes such as cell proliferation, differentiation, migration, transformation and programmed cell death. Extracellular stimuli such as proinflammatory cytokines or physical stress stimulate the stress-activated protein kinase/c-Jun N-terminal kinase (SAP/JNK) signaling pathway. In this cascade, two dual specificity kinases MAP2K4/MKK4 and MAP2K7/MKK7 phosphorylate and activate MAPK8/JNK1. In turn, MAPK8/JNK1 phosphorylates a number of transcription factors, primarily components of AP-1 such as JUN, JDP2 and ATF2 and thus regulates AP-1 transcriptional activity. Phosphorylates the replication licensing factor CDT1, inhibiting the interaction between CDT1 and the histone H4 acetylase HBO1 to replication origins. Loss of this interaction abrogates the acetylation required for replication initiation. Promotes stressed cell apoptosis by phosphorylating key regulatory factors including p53/TP53 and Yes-associates protein YAP1. In T-cells, MAPK8 and MAPK9 are required for polarized differentiation of T-helper cells into Th1 cells. Contributes to the survival of erythroid cells by phosphorylating the antagonist of cell death BAD upon EPO stimulation. Mediates starvation-induced BCL2 phosphorylation, BCL2 dissociation from BECN1, and thus activation of autophagy. Phosphorylates STMN2 and hence regulates microtubule dynamics, controlling neurite elongation in cortical neurons. In the developing brain, through its cytoplasmic activity on STMN2, negatively regulates the rate of exit from multipolar stage and of radial migration from the ventricular zone. Phosphorylates several other substrates including heat shock factor protein 4 (HSF4), the deacetylase SIRT1, ELK1, or the E3 ligase ITCH.
JNK1 isoforms display different binding patterns: beta-1 preferentially binds to c-Jun, whereas alpha-1, alpha-2, and beta-2 have a similar low level of binding to both c-Jun or ATF2. However, there is no correlation between binding and phosphorylation, which is achieved at about the same efficiency by all isoforms. -
Sequence similarities
Belongs to the protein kinase superfamily. CMGC Ser/Thr protein kinase family. MAP kinase subfamily.
Contains 1 protein kinase domain. -
Domain
The TXY motif contains the threonine and tyrosine residues whose phosphorylation activates the MAP kinases. -
Post-translational
modificationsDually phosphorylated on Thr-183 and Tyr-185 by MAP2K7 and MAP2K4, which activates the enzyme. Phosphorylated by TAOK2. -
Cellular localization
Cytoplasm. Nucleus. - Information by UniProt
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Database links
- Entrez Gene: 5599 Human
- Entrez Gene: 5601 Human
- Entrez Gene: 5602 Human
- Entrez Gene: 26414 Mouse
- Entrez Gene: 26419 Mouse
- Entrez Gene: 26420 Mouse
- Entrez Gene: 116554 Rat
- Entrez Gene: 25272 Rat
see all -
Alternative names
- C Jun kinase 2 antibody
- c Jun N terminal kinase 1 antibody
- c Jun N terminal kinase 2 antibody
see all
Images
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Immunocytochemistry/ Immunofluorescence - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (Human epithelial cells from cervix adenocarcinoma) cells labeling JNK1+JNK2+JNK3 with ab179461 at 1/250 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/400 dilution (green). Confocal image showing both cytoplasmic and nuclear staining on HeLa cells. The nuclear counterstain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows:-
-ve control 1: - ab179461 at 1/250 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2: - ab7291 (anti-Tubulin mouse mAb) at 1/500 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/400 dilution. -
![Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-234729-WBb.jpg)
Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)All lanes : Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461) at 1/20000 dilution
Lane 1 : K562 (Human chronic myelogenous leukemia cells from bone marrow) whole cell lysates
Lane 2 : HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysates
Lane 3 : Jurkat (Human T cell leukemia cells from peripheral blood) whole cell lysates
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46,54 kDa why is the actual band size different from the predicted?Blocking/Dilution buffer: 5% NFDM/TBST.
JNKs originate from three genes that yield ten isoforms through alternative mRNA splicing, including JNK1α1, JNK1β1, JNK2α1, JNK2β1 and JNK3α1, which represent the p46 isoforms, and JNK1α2, JNK1β2, JNK2α2, JNK2β2 and JNK3β2, which represent the p54 isoforms.
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![Immunocytochemistry/ Immunofluorescence - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-385352-anti-jnk-antibody-mouse-icc.jpg)
Immunocytochemistry/ Immunofluorescence - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)Formaldehyde-fixed, NP40 permeabilized Mouse Vascular smooth muscle cells stained for JNK1+JNK2+JNK3 (Green) using ab179461 at 1/200 dilution followed by a Donkey anti-rabbit Alex Fluor® 488 antibody at 1/500 dilution. The nuclear counterstain was DAPI (Blue).
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![Flow Cytometry - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-270704-Flow-cyt.jpg)
Flow Cytometry - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)Flow Cytometry analysis of HeLa (human cervix adenocarcinoma) cells labeling JNK1+JNK2+JNK3 with purified ab179461 at 1/180 dilution (10ug/mL) (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. A Goat anti rabbit IgG (Alexa Fluor® 488) (1/2000 dilution) was used as the secondary antibody. Rabbit monoclonal IgG (Black) was used as the isotype control, cells without incubation with primary antibody and secondary antibody (Blue) were used as the unlabeled control.
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![Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-234728-WBc.jpg)
Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)All lanes : Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461) at 1/5000 dilution
Lane 1 : Neuro-2a (Mouse neuroblastoma cells) whole cell lysates
Lane 2 : UMNSAH/DF-1 (Transformed chicken embyronic fibroblast cells) whole cell lysates
Lane 3 : MDCK (Canine kidney cell line) whole cell lysates
Lane 4 : MDBK (Bovine kidney cell line) whole cell lysates
Lane 5 : COS-1 (African green monkey kidney fibroblast-like cell line) whole cell lysates
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46,54 kDa why is the actual band size different from the predicted?Blocking/dilution buffer: 5% NFDM/TBST.
JNKs originate from three genes that yield ten isoforms through alternative mRNA splicing, including JNK1α1, JNK1β1, JNK2α1, JNK2β1 and JNK3α1, which represent the p46 isoforms, and JNK1α2, JNK1β2, JNK2α2, JNK2β2 and JNK3β2, which represent the p54 isoforms.
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![Immunoprecipitation - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-234807-79467.JPG)
Immunoprecipitation - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)JNK1+JNK2+JNK3 were immunoprecipitated from 1mg of Jurkat (Human T cell leukemia cells from peripheral blood) whole cell extract with ab179461 at 1/50 dilution. Western blot was performed from the immunoprecipitate using ab179461 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution. Lane 1: Jurkat whole cell extract. Lane 2: PBS instead of Jurkat whole cell extract.
Blocking and dilution buffer and concentration: 5% NFDM/TBST.JNKs originate from three genes that yield ten isoforms through alternative mRNA splicing, including JNK1α1, JNK1β1, JNK2α1, JNK2β1 and JNK3α1, which represent the p46 isoforms, and JNK1α2, JNK1β2, JNK2α2, JNK2β2 and JNK3β2, which represent the p54 isoforms.
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![Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-234730-WBa.jpg)
Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)All lanes : Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461) at 1/20000 dilution
Lane 1 : Human JNK3 full length recombinant protein containing a proprietary tag.
Lane 2 : Human JNK2 full length recombinant protein containing a proprietary tag.
Lane 3 : Human JNK1 full length recombinant protein containing a His tag.
Lysates/proteins at 0.01 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Additional bands at: 48 kDa (possible tagged protein), 71 kDa (possible tagged protein), 71 kDa (possible tagged protein)Human JNK1, JNK2 and JNK3 full length recombinant proteins are from commercial sources. JNK1 and JNK2 have a proprietary tag, JNK3 has a His tag.
Blocking/dilution buffer: 5% NFDM/TBST.
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![Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-234727-WBd.jpg)
Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)All lanes : Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461) at 1/1000 dilution
Lane 1 : Zebrafish lysate
Lane 2 : X. tropicalis lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46,54 kDa why is the actual band size different from the predicted?Blocking/dilution buffer: 5% NFDM/TBST.
Zebrafish has only one JNK isoform, JNK1 with a MW of 44kDa. So there is only one band in Zebrafish.
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![Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-234726-WBe.jpg)
Western blot - Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)All lanes : Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461) at 1/5000 dilution
Lane 1 : Mouse brain lysate
Lane 2 : Rat brain lysate
Lane 3 : Rat heart lysate
Lane 4 : RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) lysate
Lane 5 : PC-12 (Rat adrenal gland pheochromocytoma) lysate
Lane 6 : NIH/3T3 (Mouse embyro fibroblast cells) lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46,54 kDa why is the actual band size different from the predicted?Blocking/dilution buffer: 5% NFDM/TBST.
JNKs originate from three genes that yield ten isoforms through alternative mRNA splicing, including JNK1α1, JNK1β1, JNK2α1, JNK2β1 and JNK3α1, which represent the p46 isoforms, and JNK1α2, JNK1β2, JNK2α2, JNK2β2 and JNK3β2, which represent the p54 isoforms.
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![Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)](https://www.abcam.com/ps/products/179/ab179461/Images/ab179461-10-benefits-of-recombinant-antibodies.png)
Anti-JNK1+JNK2+JNK3 antibody [EPR16797-211] (ab179461)
Protocols
References (85)
ab179461 has been referenced in 85 publications.
- Jiang L et al. Inhibition of microRNA-103 attenuates inflammation and endoplasmic reticulum stress in atherosclerosis through disrupting the PTEN-mediated MAPK signaling. J Cell Physiol 235:380-393 (2020). PubMed: 31232476
- Hao Q et al. Sulforaphane suppresses carcinogenesis of colorectal cancer through the ERK/Nrf2-UDP glucuronosyltransferase 1A metabolic axis activation. Oncol Rep 43:1067-1080 (2020). PubMed: 32323779
- Fan H et al. MsrA Suppresses Inflammatory Activation of Microglia and Oxidative Stress to Prevent Demyelination via Inhibition of the NOX2-MAPKs/NF-?B Signaling Pathway. Drug Des Devel Ther 14:1377-1389 (2020). PubMed: 32308370
- Zhang Y et al. EphB4/ TNFR2/ERK/MAPK signaling pathway comprises a signaling axis to mediate the positive effect of TNF-a on osteogenic differentiation. BMC Mol Cell Biol 21:29 (2020). PubMed: 32299362
- Jia T et al. MiR-148a inhibits oral squamous cell carcinoma progression through ERK/MAPK pathway via targeting IGF-IR. Biosci Rep 40:N/A (2020). PubMed: 32202300
