PAK1/2/3 (Phospho-S144/141/139) Antibody

• Catalog Number: orb393128
• Category: Antibodies
• Description: The PAK1/2/3 (Phospho-S144/141/139) Antibody is suitable for IHC, WB. It is a Polyclonal, Unconjugated antibody which raised against KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S144/141/139 of human PAK1/2/3 protein. The exact sequence is proprietary. Purification: The antibody was purified by immunogen affinity chromatography.
• Clonality: Polyclonal
• Species/Host: Rabbit
• Conjugation: Unconjugated
• Reactivity: Human, Mouse, Rat
• Form/Appearance: Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
• Purification: The antibody was purified by immunogen affinity chromatography.
• Immunogen: KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S144/141/139 of human PAK1/2/3 protein. The exact sequence is proprietary.
• UniProt ID: Q13177, P35465, Q64303, O75914, Q62829, O88643, Q13153, Q61036, Q8CIN4
• Tested applications: IHC, WB
• Dilution range: WB: 1:500:1000, IHC-P: 1:100:200
• Antibody Type: Primary Antibody
• Storage: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
• Alternative names: PAK1; Serine/threonine-protein kinase PAK 1; Alpha
• Research Area: Apoptotic, Cancer, Epigenetics, Neuroscience, Sign
• Note: For research use only
• Entrez: 100910732, 5058, 5062, 18481, 29433, 29431, 224105, 5063

Western blot analysis of PAK1/2/3 (Phospho-S144/141/139) expression in HepG2 (A), mouse brain (B) whole cell lysates. (Predicted band size: 60; 58; 62 kD; Observed band size: 68 kD)

Immunohistochemical analysis of PAK1/2/3 (Phospho-S144/141/139) staining in human breast cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (Phospho-H 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.