Anti-Rho A + B + C antibody [EPR18299]
- RabMAb
- Recombinant
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(5 Publications)
Rabbit Recombinant Monoclonal RHOA antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Mouse, Human, Rat samples. Cited in 5 publications.
View Alternative Names
ARH12, ARHA, RHO12, RHOA, Transforming protein RhoA, Rho cDNA clone 12, h12
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Immunohistochemical analysis of paraffin-embedded Human squamous cell carcinoma of lung tissue labeling Rho A + B + C with ab188103 at 1/4000 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on cancer cells of squamous cell carcinoma of lung 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Immunohistochemical analysis of paraffin-embedded Human stomach tissue labeling Rho A + B + C with ab188103 at 1/4000 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on epithelial cells of Human stomach 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.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Intracellular flow cytometric analysis of 2% paraformaldehyde-fixed Jurkat (Human T cell leukemia cells from peripheral blood) cells labeling Rho A + B + Cwith ab188103 at 1/300 dilution (red) compared with a rabbit monoclonal IgG isotype control (black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (FITC) at 1/150 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized HepG2 (Human liver hepatocellular carcinoma) cells labeling Rho A + B + C with ab188103 at 1/500 dilution followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing both nuclear and cytoplasmic staining on HepG2 cells. The nuclear counter stain 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 : ab188103 at 1/500 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Immunohistochemical analysis of paraffin-embedded Rat colon tissue labeling Rho A + B + C with ab188103 at 1/4000 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on epithelial cells of Rat colon 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Immunohistochemical analysis of paraffin-embedded Mouse muscle tissue labeling Rho A + B + C with ab188103 at 1/4000 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on mouse muscle 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
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized NIH/3T3 (Mouse embyro fibroblast cells) cells labeling to RhoA + RhoB + RhoC with ab188103 at 1/500 dilution followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing both nuclear and cytoplasmic staining on NIH/3T3 cells. The nuclear counter stain 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 : ab188103 at 1/500 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.
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Rho A + B + C antibody [EPR18299] (ab188103) at 1/2000 dilution
Lane 1:
Human fetal brain lysate at 10 µg
Lane 2:
Human fetal kidney 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: 22 kDa
Observed band size: 22 kDa
false
Exposure time: 1min
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Rho A + B + C antibody [EPR18299] (ab188103) at 1/2000 dilution
Lane 1:
HepG2 (Human liver hepatocellular carcinoma) whole cell lysate at 10 µg
Lane 2:
HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysate at 10 µg
Lane 3:
Jurkat (Human T cell leukemia cells from peripheral blood) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 22 kDa
Observed band size: 22 kDa
false
Exposure time: 1min
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Human RhoA full length protein (Catalog# ab101594) contains aa1-193 with His-Tag® N-Terminus; Human RhoB full length protein (Catalog# ab107139) contains aa1-193 with His-Tag® N-Terminus.
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Rho A + B + C antibody [EPR18299] (ab188103) at 1/20000 dilution
Lane 1:
Human RhoA full length protein at 0.01 µg
Lane 2:
Human RhoB full length protein at 0.01 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 22 kDa
Observed band size: 24 kDa
false
Exposure time: 30s
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Human RhoC full length protein (Catalog# ab98085) contains aa1-190 with His-Tag® N-Terminus.
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Rho A + B + C antibody [EPR18299] (ab188103) at 1/500 dilution
All lanes:
Human RhoC full length protein at 0.01 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 22 kDa
Observed band size: 24 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature (PMID : 27043630).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-Rho A + B + C antibody [EPR18299] staining at 1/1000 dilution.
All lanes:
Western blot - Anti-RhoA + RhoB (ADP-ribosylated) antibody [VIF140-A1] - Mouse IgG2a (Chimeric) (<a href='/en-us/products/primary-antibodies/rhoa-rhob-adp-ribosylated-antibody-vif140-a1-mouse-igg2a-chimeric-ab324029'>ab324029</a>) at 1/1000 dilution
Lane 1:
Untreated HT-22 (mouse hippocampal neuronal cell) whole cell lysate at 20 µg
Lane 2:
HT-22 treated with 500nM C3 for 6 hours whole cell lysate at 20 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Observed band size: 22 kDa,36 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Rho A + B + C antibody [EPR18299] (ab188103) at 1/2000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Mouse kidney lysate at 10 µg
Lane 3:
Rat brain lysate at 10 µg
Lane 4:
Rat kidney lysate at 10 µg
Lane 5:
C6 (Rat glial tumor cells) whole cell lysate at 10 µg
Lane 6:
RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) whole cell lysate at 10 µg
Lane 7:
PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysate at 10 µg
Lane 8:
NIH/3T3 (Mouse embyro fibroblast cells) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 22 kDa
Observed band size: 22 kDa
false
Exposure time: 1min
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature (PMID : 27043630).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-Rho A + B + C antibody [EPR18299] staining at 1/1000 dilution.
All lanes:
Western blot - Anti-RhoA + RhoB (ADP-ribosylated) antibody [VIF140-A1] (<a href='/en-us/products/primary-antibodies/rhoa-rhob-adp-ribosylated-antibody-vif140-a1-ab324028'>ab324028</a>) at 1/1000 dilution
Lane 1:
Untreated HT-22 (mouse hippocampal neuronal cell) whole cell lysate at 20 µg
Lane 2:
HT-22 treated with 500nM C3 for 6 hours whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Human IgG Fc (HRP) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-human-igg-fc-hrp-preadsorbed-ab98624'>ab98624</a>) at 1/10000 dilution
Observed band size: 22 kDa,36 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature (PMID : 27043630).
In Western blot, Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade (ab176842) staining at 1/200000 dilution.
In Western blot, Anti-6X His tag® antibody [EPR20547] - ChIP Grade (ab213204) staining at 1/5000 dilution.
In Western blot, Anti-Rho A + B + C antibody [EPR18299] staining at 1/1000 dilution.
All lanes:
Western blot - Anti-RhoA + RhoB (ADP-ribosylated) antibody [VIF140-A1] - Mouse IgG2a (Chimeric) (<a href='/en-us/products/primary-antibodies/rhoa-rhob-adp-ribosylated-antibody-vif140-a1-mouse-igg2a-chimeric-ab324029'>ab324029</a>) at 1/1000 dilution
Lane 1:
293T (human embryonic kidney epithelial cell) transfected with an empty vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 2:
293T transfected with an empty vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Lane 3:
293T transfected with an human RhoA expression vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 4:
293T transfected with an human RhoA expression vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Lane 5:
293T transfected with an human RhoB expression vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 6:
293T transfected with an human RhoB expression vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Lane 7:
293T transfected with an human RhoC expression vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 8:
293T transfected with an human RhoC expression vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Observed band size: 22 kDa,17 kDa
false
Exposure time: 1s
- WB
Supplier Data
Western blot - Anti-Rho A + B + C antibody [EPR18299] (AB188103)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature (PMID : 27043630).
In Western blot, Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade (ab176842) staining at 1/200000 dilution.
In Western blot, Anti-6X His tag® antibody [EPR20547] - ChIP Grade (ab213204) staining at 1/5000 dilution.
In Western blot, Anti-Rho A + B + C antibody [EPR18299] staining at 1/1000 dilution.
All lanes:
Western blot - Anti-RhoA + RhoB (ADP-ribosylated) antibody [VIF140-A1] (<a href='/en-us/products/primary-antibodies/rhoa-rhob-adp-ribosylated-antibody-vif140-a1-ab324028'>ab324028</a>) at 1/1000 dilution
Lane 1:
293T (human embryonic kidney epithelial cell) transfected with an empty vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 2:
293T transfected with an empty vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Lane 3:
293T transfected with an human RhoA expression vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 4:
293T transfected with an human RhoA expression vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Lane 5:
293T transfected with an human RhoB expression vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 6:
293T transfected with an human RhoB expression vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Lane 7:
293T transfected with an human RhoC expression vector containing a myc-his-tag whole cell lysate at 20 µg
Lane 8:
293T transfected with an human RhoC expression vector containing a myc-his-tag were treated with 500nM C3 for 30 minutes whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Human IgG Fc (HRP) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-human-igg-fc-hrp-preadsorbed-ab98624'>ab98624</a>) at 1/10000 dilution
Observed band size: 22 kDa,17 kDa
false
Exposure time: 1s
Related conjugates and formulations (1)
-
Anti-Rho A + B + C antibody [EPR18299] - BSA and Azide free
Reactivity data
Product details
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
Rho proteins influence cell shape migration and adhesion. They are part of the Rho GTPase family which interacts with other molecules to form a complex that manages cellular structure. Rho proteins impact the formation of stress fibers and focal adhesions which are essential for maintaining tissue integrity and facilitating cellular responses. This activity makes Rho proteins vital players in wound healing and embryonic development.
Pathways
Rho proteins are critical parts of the Rho-ROCK (Rho-associated protein kinase) pathway and the Wnt signaling pathway. Both pathways are important for cell signaling that orchestrates changes in the cytoskeleton and cell behavior. In these pathways Rho proteins interact with kinases like ROCK1 and ROCK2 connecting to a larger network of signaling proteins that guide cellular outcomes involved in proliferation and structural maintenance.
Product protocols
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Target data
Additional targets
Publications (5)
Recent publications for all applications. Explore the full list and refine your search
The ISME journal 19: PubMed40899693
2025
Applications
Unspecified application
Species
Unspecified reactive species
Cancers 16: PubMed38791874
2024
Applications
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Species
Unspecified reactive species
Cancer management and research 12:13085-13097 PubMed33376401
2020
Applications
Unspecified application
Species
Unspecified reactive species
Frontiers in cell and developmental biology 8:254 PubMed32411702
2020
Applications
Unspecified application
Species
Unspecified reactive species
FEBS letters 591:3296-3309 PubMed28889652
2017
Applications
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Species
Unspecified reactive species
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