WB result of RhoA Recombinant Rabbit mAb
Primary antibody: RhoA Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: HeLa whole cell lysate 20 µg
Lane 2: Raji whole cell lysate 20 µg
Lane 3: K562 whole cell lysate 20 µg
Lane 4: MCF7 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 22 kDa
Observed MW: 22 kDa
Product Details
Product Details
Product Specification
Host | Rabbit |
Antigen | RhoA |
Synonyms | Transforming protein RhoA; Rho cDNA clone 12 (h12); ARH12; ARHA; RHO12 |
Immunogen | Synthetic Peptide |
Location | Cytoplasm, Nucleus, Cell membrane |
Accession | P61586 |
Clone Number | S-1310-159 |
Antibody Type | Recombinant mAb |
Isotype | IgG |
Application | WB, IHC-P, ICC |
Reactivity | Hu, Ms, Rt |
Positive Sample | HeLa, Raji, K562, MCF7, NIH/3T3, mouse brain, C6, rat brain |
Predicted Reactivity | Bv, Dg |
Purification | Protein A |
Concentration | 0.5 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
application | dilution | species |
WB | 1:1000 | Hu, Ms, Rt |
IHC-P | 1:200 | Hu, Ms, Rt |
ICC | 1:500 | Hu |
Background
RhoA is a small GTPase that plays a critical role in regulating cellular functions such as cytoskeletal structure, cell proliferation, and cell migration. It cycles between an inactive GDP-bound state and an active GTP-bound state, which is necessary to activate downstream signaling cascades. This transition relies on GDP/GTP exchange and GTP hydrolysis by regulatory proteins such as guanine nucleotide exchange factors (GEFs), GTPase-activating proteins (GAPs), and guanine nucleotide dissociation inhibitors (GDIs). Active RhoA regulates two groups of proteins: serine/threonine protein kinases, including Rho-associated, coiled-coil-containing protein kinase (ROCK), and scaffold proteins, including formin family proteins and rhotekin. RhoA is also implicated in the regulation of immune responses, cytoskeletal dynamics, cell death, and has been linked to various diseases, including neurodegenerative diseases and cardiovascular pathologies.
Picture
Picture
Western Blot
WB result of RhoA Recombinant Rabbit mAb
Primary antibody: RhoA Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: NIH/3T3 whole cell lysate 20 µg
Lane 2: mouse brain lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 22 kDa
Observed MW: 22 kDa
WB result of RhoA Recombinant Rabbit mAb
Primary antibody: RhoA Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: C6 whole cell lysate 20 µg
Lane 2: rat brain lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 22 kDa
Observed MW: 22 kDa
Immunohistochemistry
IHC shows positive staining in paraffin-embedded human colon cancer. Anti-RhoA antibody was used at 1/200 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human pancreatic cancer. Anti-RhoA antibody was used at 1/200 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded mouse kidney. Anti-RhoA antibody was used at 1/200 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded rat kidney. Anti-RhoA antibody was used at 1/200 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
Immunocytochemistry
ICC shows positive staining in HeLa cells. Anti- RhoA antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
