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Products:Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Microfilaments >> Actin etc >> Actin Assembly
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Read our guarantee »Anti-RhoA antibody
RhoA 抗体 (11件) 一覧
Rabbit polyclonal to RhoA
WB, IHC-P, IHC-Fr, FPIA, ICC/IFmore details
Reacts with
Mouse, Rat, Human
Predicted to work with
Chicken, Cow, Dog, Xenopus laevis, Zebrafish, Orangutan
Synthetic peptide (Human), conjugated to an immunogenic carrier protein
Spinal cord.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C (add glycerol to a final volume of 40% for extra stability). Avoid repeated freeze / thaw cycles.
Preservative: None
Constituents: 1X PBS
Whole antiserum
Polyclonal
IgG
Cancer >> Signal transduction >> G protein signaling >> Small G proteins >> Ras family
Signal Transduction >> Signaling Pathway >> G Protein Signaling >> Small G Proteins >> Ras Family
Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Microfilaments >> Actin etc >> Actin Assembly
Our Abpromise guarantee covers the use of ab68826 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/300 - 1/3000. Detects a band of approximately 22 kDa (predicted molecular weight: 22 kDa).
IHC-P: 1/300 - 1/3000. Antigen retrieval is recommended.
IHC-Fr: 1/300 - 1/3000.
FPIA: Use at an assay dependent concentration. PubMed: 21543326
ICC/IF: 1/200.
Regulates a signal transduction pathway linking plasma membrane receptors to the assembly of focal adhesions and actin stress fibers. Serves as a target for the yopT cysteine peptidase from Yersinia pestis, vector of the plague, and Yersinia pseudotuberculosis, which causes gastrointestinal disorders. May be an activator of PLCE1. Activated by ARHGEF2, which promotes the exchange of GDP for GTP.
Belongs to the small GTPase superfamily. Rho family.
The basic-rich region is essential for yopT recognition and cleavage.
Substrate for botulinum ADP-ribosyltransferase.
Cleaved by yopT protease when the cell is infected by some Yersinia pathogens. This removes the lipid attachment, and leads to its displacement from plasma membrane and to subsequent cytoskeleton cleavage.
AMPylation at Tyr-34 and Thr-37 are mediated by bacterial enzymes in case of infection by H.somnus and V.parahaemolyticus, respectively. AMPylation occurs in the effector region and leads to inactivation of the GTPase activity by preventing the interaction with downstream effectors, thereby inhibiting actin assembly in infected cells. It is unclear whether some human enzyme mediates AMPylation; FICD has such ability in vitro but additional experiments remain to be done to confirm results in vivo.
Ubiquitinated by the BCR(BACURD1) and BCR(BACURD2) E3 ubiquitin ligase complexes, leading to its degradation by the proteasome, thereby regulating the actin cytoskeleton and cell migration.
Cell membrane. Cytoplasm > cytoskeleton.
Target information above from: UniProt accessionP61586
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - RhoA antibody (ab68826)

Lane 1 : Anti-RhoA antibody (ab68826) at 1/2000 dilution
Lane 2 : Anti-RhoA antibody (ab68826) at 1/2000 dilution (pre-absorbed with immunizing peptide)
Lane 1 : Rat spinal cord lysate
Lane 2 : Rat spinal cord lysate
Predicted band size : 22 kDa
Observed band size : 22 kDa
Immunohistochemistry (Frozen sections) - RhoA antibody (ab68826)

ab68826 (1/500) staining RhoA (red) and ab72019 staining Sortilin (green) in rat trigeminal tissue. DAPI counterstaining appears in blue.
Immunocytochemistry/ Immunofluorescence - RhoA antibody (ab68826)

ICC/IF image of ab68826 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab68826 1/200 dilution overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti- rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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See all 2 publications for this product
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ab68826 (1/500) staining RhoA (red) and ab72019 staining Sortilin (green) in rat trigeminal tissue. DAPI counterstaining appears in blue.

ICC/IF image of ab68826 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab68826 1/200 dilution overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti- rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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