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monoclonal rac1 antibodies  (Cytoskeleton Inc)


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    Structured Review

    Cytoskeleton Inc monoclonal rac1 antibodies
    White blood cell motility is critical for the inflammatory response to infection. The regulation of the actin cytoskeleton by Rho family GTPases (e.g., <t>Rac1)</t> and their kinases is crucial for leukocyte migration to sites of inflammation, making them essential biomarkers for identifying sources of bacteremia. (A) White blood cells include PMN: polymorphonuclear cells (neutrophils, eosinophils, and basophils) and PBMC: peripheral blood mononuclear cells (lymphocytes, monocytes, natural killer cells, and dendritic cells). Image courtesy of Visible Body ( https://www.visiblebody.com/learn/biology/blood-cells/blood-overview ). A complete blood count with differential reflects changes in leukocyte counts caused by various pathogens. (B) The separation of whole blood components using a Ficoll gradient allows for the isolation of PMNs and PBMCs, which are subsequently analyzed with the G-Trap assay that quantitatively measures activated Rac1 (Rac1•GTP) levels in lysates of PBMCs and PMNs. (C) Serial analysis of PBMCs from representative patients with an active immune response to bacteremia revealed that two patients were resistant to broad-spectrum antibiotic treatment, while one responded positively. Additionally, one patient exhibited immune suppression, as indicated by low Rac1•GTP levels.
    Monoclonal Rac1 Antibodies, supplied by Cytoskeleton Inc, used in various techniques. Bioz Stars score: 94/100, based on 239 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+anti+rac1+antibody/Anti-Rac1+mouse+Mab/pmc11876111-170-0-9
    Average 94 stars, based on 239 article reviews
    monoclonal rac1 antibodies - by Bioz Stars, 2026-10
    94/100 stars

    Images

    1) Product Images from "A model for predicting bacteremia species based on host immune response"

    Article Title: A model for predicting bacteremia species based on host immune response

    Journal: Frontiers in Cellular and Infection Microbiology

    doi: 10.3389/fcimb.2025.1451293

    White blood cell motility is critical for the inflammatory response to infection. The regulation of the actin cytoskeleton by Rho family GTPases (e.g., Rac1) and their kinases is crucial for leukocyte migration to sites of inflammation, making them essential biomarkers for identifying sources of bacteremia. (A) White blood cells include PMN: polymorphonuclear cells (neutrophils, eosinophils, and basophils) and PBMC: peripheral blood mononuclear cells (lymphocytes, monocytes, natural killer cells, and dendritic cells). Image courtesy of Visible Body ( https://www.visiblebody.com/learn/biology/blood-cells/blood-overview ). A complete blood count with differential reflects changes in leukocyte counts caused by various pathogens. (B) The separation of whole blood components using a Ficoll gradient allows for the isolation of PMNs and PBMCs, which are subsequently analyzed with the G-Trap assay that quantitatively measures activated Rac1 (Rac1•GTP) levels in lysates of PBMCs and PMNs. (C) Serial analysis of PBMCs from representative patients with an active immune response to bacteremia revealed that two patients were resistant to broad-spectrum antibiotic treatment, while one responded positively. Additionally, one patient exhibited immune suppression, as indicated by low Rac1•GTP levels.
    Figure Legend Snippet: White blood cell motility is critical for the inflammatory response to infection. The regulation of the actin cytoskeleton by Rho family GTPases (e.g., Rac1) and their kinases is crucial for leukocyte migration to sites of inflammation, making them essential biomarkers for identifying sources of bacteremia. (A) White blood cells include PMN: polymorphonuclear cells (neutrophils, eosinophils, and basophils) and PBMC: peripheral blood mononuclear cells (lymphocytes, monocytes, natural killer cells, and dendritic cells). Image courtesy of Visible Body ( https://www.visiblebody.com/learn/biology/blood-cells/blood-overview ). A complete blood count with differential reflects changes in leukocyte counts caused by various pathogens. (B) The separation of whole blood components using a Ficoll gradient allows for the isolation of PMNs and PBMCs, which are subsequently analyzed with the G-Trap assay that quantitatively measures activated Rac1 (Rac1•GTP) levels in lysates of PBMCs and PMNs. (C) Serial analysis of PBMCs from representative patients with an active immune response to bacteremia revealed that two patients were resistant to broad-spectrum antibiotic treatment, while one responded positively. Additionally, one patient exhibited immune suppression, as indicated by low Rac1•GTP levels.

    Techniques Used: Infection, Migration, Isolation, TRAP Assay

    Related Articles

    Incubation:

    Article Title: The pivotal role of CCN2 in mammalian palatogenesis.
    Article Snippet: Protein concentration of lysates was determined using Pierce BCA Protein Assay Kit (23225, Thermo Scientific, Rockford, IL). .. Membranes were blocked with 5 % bovine serum albumin (BSA) (BP1605, Fisher Scientific, Fair Lawn, NJ) solution in 1X TBS-T (0.1 % Tween 20 (X251-07, JT Baker, Center Valley, PA)) for 1 h at room temperature and then incubated with a goat polyclonal anti-CTGF antibody (sc-14939 Santa Cruz, Dallas, Tx) diluted 1:200, mouse monoclonal anti-Rac1 antibody (ARC03 Cytoskeleton, Denver, CO) diluted 1:500, mouse monoclonal ant i -RhoA antibody (ARH04 Cytoskeleton, Denver, CO) diluted 1:500, or Rabbit antiActin antibody (A2066, Sigma, St. Louis, MO) in blocking buffer overnight at 4 °C. .. Membranes were washed with 1X TBS-T (0.1 % Tween 20) and incubated with Donkey antigoat IRDye ® 800 CW (1:5000) (925–32214, Licor, Lincoln, NE), Donkey anti-Mouse HRP (1:5000) (715-035-50, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA), or Donkey anti-Rabbit HRP (1:5000) (711-035-152, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA) secondary antibodies diluted in blocking buffer.

    Article Title: The pivotal role of CCN2 in mammalian palatogenesis
    Article Snippet: Protein concentration of lysates was determined using Pierce BCA Protein Assay Kit (23225, Thermo Scientific, Rockford, IL). .. Membranes were blocked with 5 % bovine serum albumin (BSA) (BP1605, Fisher Scientific, Fair Lawn, NJ) solution in 1X TBS-T (0.1 % Tween 20 (X251-07, JT Baker, Center Valley, PA)) for 1 h at room temperature and then incubated with a goat polyclonal anti-CTGF antibody (sc-14939 Santa Cruz, Dallas, Tx) diluted 1:200, mouse monoclonal anti-Rac1 antibody (ARC03 Cytoskeleton, Denver, CO) diluted 1:500, mouse monoclonal anti-RhoA antibody (ARH04 Cytoskeleton, Denver, CO) diluted 1:500, or Rabbit anti-Actin antibody (A2066, Sigma, St. Louis, MO) in blocking buffer overnight at 4 °C. .. Membranes were washed with 1X TBS-T (0.1 % Tween 20) and incubated with Donkey anti-goat IRDye ® 800 CW (1:5000) (925–32214, Licor, Lincoln, NE), Donkey anti-Mouse HRP (1:5000) (715-035-50, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA), or Donkey anti-Rabbit HRP (1:5000) (711-035-152, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA) secondary antibodies diluted in blocking buffer.

    Blocking Assay:

    Article Title: The pivotal role of CCN2 in mammalian palatogenesis.
    Article Snippet: Protein concentration of lysates was determined using Pierce BCA Protein Assay Kit (23225, Thermo Scientific, Rockford, IL). .. Membranes were blocked with 5 % bovine serum albumin (BSA) (BP1605, Fisher Scientific, Fair Lawn, NJ) solution in 1X TBS-T (0.1 % Tween 20 (X251-07, JT Baker, Center Valley, PA)) for 1 h at room temperature and then incubated with a goat polyclonal anti-CTGF antibody (sc-14939 Santa Cruz, Dallas, Tx) diluted 1:200, mouse monoclonal anti-Rac1 antibody (ARC03 Cytoskeleton, Denver, CO) diluted 1:500, mouse monoclonal ant i -RhoA antibody (ARH04 Cytoskeleton, Denver, CO) diluted 1:500, or Rabbit antiActin antibody (A2066, Sigma, St. Louis, MO) in blocking buffer overnight at 4 °C. .. Membranes were washed with 1X TBS-T (0.1 % Tween 20) and incubated with Donkey antigoat IRDye ® 800 CW (1:5000) (925–32214, Licor, Lincoln, NE), Donkey anti-Mouse HRP (1:5000) (715-035-50, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA), or Donkey anti-Rabbit HRP (1:5000) (711-035-152, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA) secondary antibodies diluted in blocking buffer.

    Article Title: The pivotal role of CCN2 in mammalian palatogenesis
    Article Snippet: Protein concentration of lysates was determined using Pierce BCA Protein Assay Kit (23225, Thermo Scientific, Rockford, IL). .. Membranes were blocked with 5 % bovine serum albumin (BSA) (BP1605, Fisher Scientific, Fair Lawn, NJ) solution in 1X TBS-T (0.1 % Tween 20 (X251-07, JT Baker, Center Valley, PA)) for 1 h at room temperature and then incubated with a goat polyclonal anti-CTGF antibody (sc-14939 Santa Cruz, Dallas, Tx) diluted 1:200, mouse monoclonal anti-Rac1 antibody (ARC03 Cytoskeleton, Denver, CO) diluted 1:500, mouse monoclonal anti-RhoA antibody (ARH04 Cytoskeleton, Denver, CO) diluted 1:500, or Rabbit anti-Actin antibody (A2066, Sigma, St. Louis, MO) in blocking buffer overnight at 4 °C. .. Membranes were washed with 1X TBS-T (0.1 % Tween 20) and incubated with Donkey anti-goat IRDye ® 800 CW (1:5000) (925–32214, Licor, Lincoln, NE), Donkey anti-Mouse HRP (1:5000) (715-035-50, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA), or Donkey anti-Rabbit HRP (1:5000) (711-035-152, Jackson ImmunoResearch Laboratories, Inc, West Grove, PA) secondary antibodies diluted in blocking buffer.

    Western Blot:

    Article Title: Integrin Mediated Adhesion of Osteoblasts to Connective Tissue Growth Factor (CTGF/CCN2) Induces Cytoskeleton Reorganization and Cell Differentiation
    Article Snippet: .. Western Blot analysis was performed on the samples using a mouse monoclonal anti-Rac1 antibody (Cytoskeleton). .. When the MC3T3-E1 cells in the culture dishes were 70% confluent culture dishes, they were harvested and the cells were lysed with1X RIPA lyses buffer (Millipore) containing 1% protease inhibitor (Sigma-Aldrich).

    Article Title: Integrin mediated adhesion of osteoblasts to connective tissue growth factor (CTGF/CCN2) induces cytoskeleton reorganization and cell differentiation.
    Article Snippet: .. Western Blot analysis was performed on the samples using a mouse monoclonal anti-Rac1 antibody (Cytoskeleton). .. Co-Immunoprecipitation When the MC3T3-E1 cells in the culture dishes were 70% confluent culture dishes, they were harvested and the cells were lysed with1X RIPA lyses buffer (Millipore) containing 1% protease inhibitor (Sigma-Aldrich).

    other:

    Article Title: Rac1 S71 Mediates the Interaction between Rac1 and 14-3-3 Proteins.
    Article Snippet: Mouse monoclonal anti-Rac1 antibody was purchased from Cytoskeleton Inc. (Denver, CO, USA).

    Article Title: Phosphorylation of Rac1 T108 by Extracellular Signal-Regulated Kinase in Response to Epidermal Growth Factor: a Novel Mechanism To Regulate Rac1 Function
    Article Snippet: Mouse monoclonal anti-Rac1 antibody was purchased from Cytoskeleton, Inc. (Denver, CO).

    Article Title: Rac1 S71 Mediates the Interaction between Rac1 and 14-3-3 Proteins
    Article Snippet: Mouse monoclonal anti-Rac1 antibody was purchased from Cytoskeleton Inc. (Denver, CO, USA).



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    Image Search Results


    White blood cell motility is critical for the inflammatory response to infection. The regulation of the actin cytoskeleton by Rho family GTPases (e.g., Rac1) and their kinases is crucial for leukocyte migration to sites of inflammation, making them essential biomarkers for identifying sources of bacteremia. (A) White blood cells include PMN: polymorphonuclear cells (neutrophils, eosinophils, and basophils) and PBMC: peripheral blood mononuclear cells (lymphocytes, monocytes, natural killer cells, and dendritic cells). Image courtesy of Visible Body ( https://www.visiblebody.com/learn/biology/blood-cells/blood-overview ). A complete blood count with differential reflects changes in leukocyte counts caused by various pathogens. (B) The separation of whole blood components using a Ficoll gradient allows for the isolation of PMNs and PBMCs, which are subsequently analyzed with the G-Trap assay that quantitatively measures activated Rac1 (Rac1•GTP) levels in lysates of PBMCs and PMNs. (C) Serial analysis of PBMCs from representative patients with an active immune response to bacteremia revealed that two patients were resistant to broad-spectrum antibiotic treatment, while one responded positively. Additionally, one patient exhibited immune suppression, as indicated by low Rac1•GTP levels.

    Journal: Frontiers in Cellular and Infection Microbiology

    Article Title: A model for predicting bacteremia species based on host immune response

    doi: 10.3389/fcimb.2025.1451293

    Figure Lengend Snippet: White blood cell motility is critical for the inflammatory response to infection. The regulation of the actin cytoskeleton by Rho family GTPases (e.g., Rac1) and their kinases is crucial for leukocyte migration to sites of inflammation, making them essential biomarkers for identifying sources of bacteremia. (A) White blood cells include PMN: polymorphonuclear cells (neutrophils, eosinophils, and basophils) and PBMC: peripheral blood mononuclear cells (lymphocytes, monocytes, natural killer cells, and dendritic cells). Image courtesy of Visible Body ( https://www.visiblebody.com/learn/biology/blood-cells/blood-overview ). A complete blood count with differential reflects changes in leukocyte counts caused by various pathogens. (B) The separation of whole blood components using a Ficoll gradient allows for the isolation of PMNs and PBMCs, which are subsequently analyzed with the G-Trap assay that quantitatively measures activated Rac1 (Rac1•GTP) levels in lysates of PBMCs and PMNs. (C) Serial analysis of PBMCs from representative patients with an active immune response to bacteremia revealed that two patients were resistant to broad-spectrum antibiotic treatment, while one responded positively. Additionally, one patient exhibited immune suppression, as indicated by low Rac1•GTP levels.

    Article Snippet: Monoclonal Rac1 antibodies (Cat. # ARC03) were purchased from Cytoskeleton.

    Techniques: Infection, Migration, Isolation, TRAP Assay