Synthetic peptide corresponding to residues at the carboxy terminus of human IKKß protein
Conjugate
Unconjugated
Applications
Application Notes
Recommended dilution: WB: 1:1000
Images
Western blot analysis of IKBKB was performed with 10 µg of A549 cells transfected with Transfection Reagent alone (Lane 1), 100nM Non-Targeting control siRNA (Lane 2), or 100nM siRNA against IKBKB (Lane 3). Proteins were resolved using a NuPAGE® Novex 4-12% Bis-Tris Gel , XCell SureLock™ Electrophoresis System , and a protein size ladder. Proteins were wet transferred to a Pierce Nitrocellulose Membrane OR Pierce PVDF Membrane and blocked with Pierce Starting Block T20 (PBS) Blocking Buffer for 1 hour at room temperature. IKBKB was detected at ~ 87 kDa using IKBKB Rabbit monoclonal antibody diluted in Pierce Starting Block T20 (PBS) Blocking Buffer 4°C overnight on a rocking platform. Pierce Goat Anti-Rabbit HRP-Conjugated Antibodies at a 1:2500 dilution were used and chemiluminescent detection was performed using Pierce Supersignal West Dura Maximum Sensitivity Substrate. Relative density of the bands normalized to GAPDH (36 kDa). IKBKB Antibody confirms silencing of IKBKB expression.
We offer labeled antibodies using our catalogue antibody products and a broad range of intensely fluorescent dyes and labels including HRP, biotin, ALP, Alexa Fluor® dyes, DyLight® Fluor dyes, R-phycoerythrin (R-PE), at scales from less than 100 μg up to 1 g of IgG antibody. Learn More
Citations
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Garimella, SV; Gehlhaus, K; et al. Identification of novel molecular regulators of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis in breast cancer cells by RNAi screening. BREAST CANCER RESEARCH 16:-(2014).
Li, W; Li, H; et al. Tumor Necrosis Factor Stimulates Matrix Metalloproteinase 9 Secretion from Cultured Human Chorionic Trophoblast Cells Through TNF Receptor 1 Signaling to IKBKB-NFKB and MAPK1/3 Pathway. BIOLOGY OF REPRODUCTION 83:481-487(2010).
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Anti-Human IKK beta monoclonal antibody
Western blot analysis of IKBKB was performed with 10 µg of A549 cells transfected with Transfection Reagent alone (Lane 1), 100nM Non-Targeting control siRNA (Lane 2), or 100nM siRNA against IKBKB (Lane 3). Proteins were resolved using a NuPAGE® Novex 4-12% Bis-Tris Gel , XCell SureLock™ Electrophoresis System , and a protein size ladder. Proteins were wet transferred to a Pierce Nitrocellulose Membrane OR Pierce PVDF Membrane and blocked with Pierce Starting Block T20 (PBS) Blocking Buffer for 1 hour at room temperature. IKBKB was detected at ~ 87 kDa using IKBKB Rabbit monoclonal antibody diluted in Pierce Starting Block T20 (PBS) Blocking Buffer 4°C overnight on a rocking platform. Pierce Goat Anti-Rabbit HRP-Conjugated Antibodies at a 1:2500 dilution were used and chemiluminescent detection was performed using Pierce Supersignal West Dura Maximum Sensitivity Substrate. Relative density of the bands normalized to GAPDH (36 kDa). IKBKB Antibody confirms silencing of IKBKB expression.
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