Anti-JNK1 + JNK2 + JNK3 抗体 [EPR16797-211]
Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211]
- 20ul selling size
- RabMAb
- Recombinant
- 詳細を見る
4
(8 Reviews)
|
(326 Publications)
Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (ab179461) is a rabbit monoclonal antibody detecting JNK1 + JNK2 + JNK3 in Western Blot, Flow Cytometry (Intra), IP, ICC/IF. Suitable for Chicken, Cow, Dog, Human, Mouse, Rat, Monkey, Xenopus, Zebrafish.
- Biophysical QC for unrivalled batch-batch consistency
- Over 220 publications
別名を表示する
JNK1, PRKM8, SAPK1, SAPK1C, MAPK8, Mitogen-activated protein kinase 8, MAP kinase 8, MAPK 8, JNK-46, Stress-activated protein kinase 1c, Stress-activated protein kinase JNK1, c-Jun N-terminal kinase 1, SAPK1c, JNK3, JNK3A, PRKM10, SAPK1B, MAPK10, Mitogen-activated protein kinase 10, MAP kinase 10, MAPK 10, MAP kinase p49 3F12, Stress-activated protein kinase 1b, Stress-activated protein kinase JNK3, c-Jun N-terminal kinase 3, SAPK1b, JNK2, PRKM9, SAPK1A, MAPK9, Mitogen-activated protein kinase 9, MAP kinase 9, MAPK 9, JNK-55, Stress-activated protein kinase 1a, Stress-activated protein kinase JNK2, c-Jun N-terminal kinase 2, SAPK1a
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (AB179461)
Intracellular 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.
- ICC/IF
Supplier Data
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.
- IP
Supplier Data
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.
All lanes:
Immunoprecipitation - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (ab179461)
Predicted band size: 48 kDa
false
- ICC/IF
Supplier Data
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).
- WB
Supplier Data
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (AB179461)
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.
All lanes:
Western blot - 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 at 20 µg
Lane 2:
HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysates at 20 µg
Lane 3:
Jurkat (Human T cell leukemia cells from peripheral blood) whole cell lysates at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46 kDa,54 kDa
false
- WB
Supplier Data
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (AB179461)
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.
All lanes:
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (ab179461) at 1/20000 dilution
Lane 1:
Human JNK3 full length recombinant protein containing a proprietary tag. at 0.01 µg
Lane 2:
Human JNK2 full length recombinant protein containing a proprietary tag. at 0.01 µg
Lane 3:
Human JNK1 full length recombinant protein containing a His tag. at 0.01 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 48 kDa,71 kDa
false
- WB
Supplier Data
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (AB179461)
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.
All lanes:
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (ab179461) at 1/5000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Rat brain lysate at 10 µg
Lane 3:
Rat heart lysate at 10 µg
Lane 4:
RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) lysate at 10 µg
Lane 5:
PC-12 (Rat adrenal gland pheochromocytoma) lysate at 10 µg
Lane 6:
NIH/3T3 (Mouse embyro fibroblast cells) lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46 kDa,54 kDa
false
- WB
Supplier Data
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (AB179461)
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.
All lanes:
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (ab179461) at 1/5000 dilution
Lane 1:
Neuro-2a (Mouse neuroblastoma cells) whole cell lysates at 10 µg
Lane 2:
UMNSAH/DF-1 (Transformed chicken embyronic fibroblast cells) whole cell lysates at 10 µg
Lane 3:
MDCK (Canine kidney cell line) whole cell lysates at 10 µg
Lane 4:
MDBK (Bovine kidney cell line) whole cell lysates at 10 µg
Lane 5:
COS-1 (African green monkey kidney fibroblast-like cell line) whole cell lysates at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46 kDa,54 kDa
false
- WB
Supplier Data
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (AB179461)
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.
All lanes:
Western blot - Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (ab179461) at 1/1000 dilution
Lane 1:
Zebrafish lysate at 10 µg
Lane 2:
X. tropicalis lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 48 kDa
Observed band size: 46 kDa,54 kDa
false
関連する標識済み抗体及び組成の異なる製品 (4)
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Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] - BSA and Azide free (Capture)
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Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] - BSA and Azide free
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211]
Reactivity data
製品の詳細
What is this antibody validated in?
Anti-JNK1 + JNK2 + JNK3 antibody [EPR16797-211] (ab179461) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Flow Cytometry (Intra), Flow Cytometry (Flow Cyt), Immunoprecipitation (IP), Immunocytochemistry/immunofluorescence (ICC/IF) in African green monkey, Chicken, Cow, Dog, Human, Mouse, Rat, Xenopus tropicalis, Zebrafish samples.
What is the molecular weight of JNK1 + JNK2 + JNK3?
Anti-JNK1 + JNK2 + JNK3 [EPR16797-211] (ab179461) specifically detects a band for JNK1 + JNK2 + JNK3 (UniProt: P45983) at a molecular weight of 48kDa.
Trusted by the scientific community
Anti-JNK1 + JNK2 + JNK3 [EPR16797-211] (ab179461) was first used in a scientific publication in 2014 and has been cited over 220 times in peer-reviewed journals.
Reviewed by scientists
Anti-JNK1 + JNK2 + JNK3 [EPR16797-211] (ab179461) has over 5 independent reviews from customers.
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 [EPR16797-211] also available for your convenience: ab179461, Carrier free - ab225572, Alexa Fluor® 488 - ab315841, Alexa Fluor® 647 - ab315842
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.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存期間
短期保存温度
長期保存温度
分注に関する情報
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補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
These kinases function as significant regulators of cellular responses to stress and cytokines. They do not act alone but often form part of larger signaling complexes that include other MAPKs and various scaffold proteins. Their roles are substantial in cell differentiation proliferation apoptosis and migration. Precise regulation by JNK molecules influences these critical cellular events which play a role in maintaining homeostasis and response to external stresses.
Pathways
JNK proteins are central to the MAPK signaling pathway and are tightly linked to the MAPK/ERK pathway. Activation of the JNK pathways leads to the regulation of various other proteins including those in the apoptosis pathway such as Bcl-2 and Bax. These interactions focus on cellular stress response regulation and contribute to processes like inflammation stress-induced apoptosis and some metabolic processes.
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文献 (326)
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