Key features and details
- Mouse monoclonal [1B34A10] to RhoA + C
- Suitable for: IP, ICC/IF, WB
- Reacts with: Mouse, Human
- Isotype: IgG
Product nameAnti-RhoA + C antibody [1B34A10]
DescriptionMouse monoclonal [1B34A10] to RhoA + C
Tested applicationsSuitable for: IP, ICC/IF, WBmore details
Species reactivityReacts with: Mouse, Human
Recombinant full length protein corresponding to Human RhoA + C aa 1-193.
MAAIRKKLVIVGDGACGKTCLLIVFSKDQFPEVYVPTVFENYVADIEVDG KQVELALWDTAGQEDYDRLRPLSYPDTDVILMCFSIDSPDSLENIPEKWT PEVKHFCPNVPIILVGNKKDLRNDEHTRRELAKMKQEPVKPEEGRDMANR IGAFGYMECSAKTKDGVREVFEMATRAALQARRGKKKSGCLVL
Database link: P61586
- HeLa, A431, HEK293T, NIH 3T3, U2 OS and K562 whole cell lysates; RhoA and RhoC recombinant proteins; HeLa cells.
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We are also updating the applications & species that this product has been “predicted to work with,” however this information is not covered by our Abpromise guarantee.
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Storage instructionsShipped 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 bufferPreservative: 0.05% Sodium azide
Constituents: 0.1% BSA, 30% Glycerol (glycerin, glycerine), 69% PBS
Concentration information loading...
PurityProtein A purified
Our Abpromise guarantee covers the use of ab175359 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|IP||Use at an assay dependent concentration.
|ICC/IF||1/100 - 1/200.|
|WB||1/500 - 1/1500. Predicted molecular weight: 22 kDa.|
RelevanceRhoA regulates a signal transduction pathway linking plasma membrane receptors to the assembly of focal adhesions and actin stress fibers. Involved in a microtubule-dependent signal that is required for the myosin contractile ring formation during cell cycle cytokinesis. Plays an essential role in cleavage furrow formation. Required for the apical junction formation of keratinocyte cell-cell adhesion. Serves as a target for the yopT cysteine peptidase from Yersinia pestis, vector of the plague, and Yersinia pseudotuberculosis, which causes gastrointestinal disorders. Stimulates PKN2 kinase activity. May be an activator of PLCE1. Activated by ARHGEF2, which promotes the exchange of GDP for GTP. Essential for the SPATA13-mediated regulation of cell migration and adhesion assembly and disassembly. The MEMO1-RHOA-DIAPH1 signaling pathway plays an important role in ERBB2-dependent stabilization of microtubules at the cell cortex. It controls the localization of APC and CLASP2 to the cell membrane, via the regulation of GSK3B activity. In turn, membrane-bound APC allows the localization of the MACF1 to the cell membrane, which is required for microtubule capture and stabilization. RhoC regulates a signal transduction pathway linking plasma membrane receptors to the assembly of focal adhesions and actin stress fibers. Serves as a microtubule-dependent signal that is required for the myosin contractile ring formation during cell cycle cytokinesis. Regulates apical junction formation in bronchial epithelial cells.
Cellular localizationRhoA: Cell membrane; Lipid-anchor; Cytoplasmic side. Cytoplasm; cytoskeleton. Cleavage furrow. Cytoplasm; cell cortex. Midbody. RhoC:Cell membrane; Lipid-anchor; Cytoplasmic side Potential. Cleavage furrow.
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All lanes : Anti-RhoA + C antibody [1B34A10] (ab175359) at 1/1000 dilution
Lane 1 : HeLa whole cell lysate at 25 µg
Lane 2 : A431 whole cell lysate at 25 µg
Lane 3 : HEK293T whole cell lysate at 25 µg
Lane 4 : U2 OS whole cell lysate at 25 µg
Lane 5 : NIH 3T3 whole cell lysate at 25 µg
Lane 6 : K562 whole cell lysate at 25 µg
Lane 7 : RhoA purified protein at 0.5 µg
Lane 8 : RhoB purified protein at 0.5 µg
Lane 9 : RhoC purified protein with proprietary tag at 0.5 µg
All lanes : goat anti-mouse IgG-HRP at 1/15000 dilution
Developed using the ECL technique.
Predicted band size: 22 kDa
Immunofluorescent analysis of HeLa cells (formalin-fixed, 0.1% Triton X-100 permeabilized) labeling RhoA + C with ab175359 at 1/100 dilution followed with DyLight 488 goat anti-mouse IgG secondary antibody at 1/400 dilution. Nuclei (blue) were stained with Hoechst 33342 dye.
Immunoprecipitation analysis of RhoA + C was performed on HeLa cells. Antigen-antibody complexes were formed by incubating 500μg of whole cell lysate with 2μg ab175359 (lane 2).
HeLa cell lysate was run as a control (lane 1).
For WB detection, ab175359 was used at 1/1000 dilution.
ab175359 has not yet been referenced specifically in any publications.