Anti-MEK3 + MEK6 抗体 [EPR17340]
Anti-MEK3 + MEK6 antibody [EPR17340]
- RabMAb
- Recombinant
- 了解详情
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(4 Publications)
Rabbit Recombinant Monoclonal MEK3 antibody. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra), IHC-P and reacts with Human, Mouse, Rat, Recombinant fragment - Human samples. Cited in 4 publications.
查看别名
MEK3, MKK3, PRKMK3, SKK2, MAP2K3, Dual specificity mitogen-activated protein kinase kinase 3, MAP kinase kinase 3, MAPKK 3, MAPK/ERK kinase 3, Stress-activated protein kinase kinase 2, MEK 3, SAPK kinase 2, SAPKK-2, SAPKK2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Immunohistochemical analysis of paraffin-embedded Human spleen tissue labeling MEK3 + MEK6 with ab200831 at 1/250 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Nuclear and cytoplasmic staining on Human spleen tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Immunocytochemistry analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HepG2 (human hepatocellular carcinoma) cells labeling MEK3 + MEK6 with ab200831 at 1/1000 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Nuclear and cytoplasmic staining on HepG2 cell line is observed. The nuclear counterstain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows : -
-ve control 1 : ab200831 at 1/1000 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Intracellular Flow Cytometry analysis of HeLa cells labelling MEK3 + MEK6 (red) with purified ab200831 at dilution of 1/150. The secondary antibody used was Alexa Fluorr® 488 goat-anti-rabbit IgG (1/2000). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Isotype control antibody was Rabbit monoclonal IgG (black). The blue line shows cells without incubation with primary antibody and secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Immunohistochemical analysis of paraffin-embedded Human cervix carcinoma tissue labeling MEK3 + MEK6 with ab200831 at 1/250 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Nuclear and cytoplasmic staining on Human cervix carcinoma tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IP
Supplier Data
Immunoprecipitation - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
MEK3 + MEK6 was immunoprecipitated from 1mg of HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysate with ab200831 at 1/100 dilution. Western blot was performed from the immunoprecipitate using ab200831 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 : HeLa whole cell lysate 10ug (Input). Lane 2 : ab200831 IP in HeLa whole cell lysate. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab200831 in Jurkat whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 30 seconds.
All lanes:
Immunoprecipitation - Anti-MEK3 + MEK6 antibody [EPR17340] (ab200831)
Predicted band size: 39 kDa
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling MEK3 + MEK6 with ab200831 at 1/250 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Nuclear and cytoplasmic staining on Mouse liver tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- WB
Supplier Data
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Blocking/Dilution Buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (ab200831) at 1/1000 dilution
Lane 1:
HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
HepG2 (Human liver hepatocellular carcinoma) whole cell lysate at 20 µg
Lane 3:
Jurkat (Human T cell leukemia cells from peripheral blood) whole cell lysate at 20 µg
Lane 4:
MCF7 (Human breast adenocarcinoma cell line) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 39 kDa
Observed band size: 34 kDa,37 kDa,39 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Blocking/Dilution Buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (ab200831) at 1/10000 dilution
All lanes:
Human fetal liver tissue lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 39 kDa
Observed band size: 34 kDa,37 kDa,39 kDa
false
Exposure time: 1min
- WB
Supplier Data
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Blocking/Dilution buffer : 5% NFDM/TBST.
Recombinant fragment of Human MEK6 protein contains aa139-334 with His-Tag®(22kDa).
All lanes:
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (ab200831) at 1/10000 dilution
All lanes:
Human MEK6 recombinant protein fragment at 10 µg
Predicted band size: 39 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (AB200831)
Blocking/Dilution Buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-MEK3 + MEK6 antibody [EPR17340] (ab200831) at 1/1000 dilution
Lane 1:
Mouse spleen lysate at 10 µg
Lane 2:
Rat spleen lysate at 10 µg
Lane 3:
C6 (Rat glial tumor cells) whole cell lysate
Lane 4:
RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) whole cell lysate
Lane 5:
PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysate
Lane 6:
NIH/3T3 (Mouse embyro fibroblast cells) whole cell lysate
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 39 kDa
Observed band size: 34 kDa,37 kDa,39 kDa
false
Exposure time: 30s
不同偶联物与剂型 (2)
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Anti-MEK3 + MEK6 antibody [EPR17340] - BSA and Azide free (Capture)
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Anti-MEK3 + MEK6 antibody [EPR17340] - BSA and Azide free
反应性数据
产品详情
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
MEK3 and MEK6 are key components of the MAP kinase signaling pathway. These kinases participate in response networks that regulate stress-induced signaling and inflammatory responses. Although not explicitly forming a classic complex they interact with substrates like p38 MAPK to exert their effects. MEK3 and MEK6 contribute to cellular processes including differentiation apoptosis and gene expression.
Pathways
MEK3 and MEK6 are integral to the p38 MAPK pathway and the stress-activated protein kinase (SAPK) pathways. These pathways facilitate the cellular response to external stress hypoxia and inflammatory cytokines. Their activity is closely related to other MAP kinases like JNK in propagating signals that control cellular stress responses. Their activation mechanism involves sequential phosphorylation events that link initial stimuli to specific cellular reactions.
产品实验方案
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靶点信息
其他靶点
文献 (4)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 14:861 PubMed36792623
2023
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Pharmaceutical biology 60:570-578 PubMed35244521
2022
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Journal of cachexia, sarcopenia and muscle 11:1104-1120 PubMed32096609
2020
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Cell death & disease 9:699 PubMed29899528
2018
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