Anti-Murine TNF-α (Polyclonal Goat) 0 ReviewsSubmit a Review Product Details Catalogue Number: 500-P64G Description: Source: Polyclonal Goat Preparation: Produced from sera of goats pre-immunized with highly pure recombinant Murine TNF-α. Anti-Murine TNF-α specific antibody was purified by affinity chromatography employing immobilized Murine TNF-α matrix. Immunogen: E.coli derived Recombinant Murine TNF-α (PeproTech catalog# 315-01A) Sandwich ELISA: To detect Murine TNF-α by sandwich ELISA (using 100 μl/well antibody solution) a concentration of 0.5 - 2.0 μg/ml of this antibody is required. This antigen affinity purified antibody, in conjunction with PeproTech’s Biotinylated Anti-Murine TNF-α (500-P64GBt) as a detection antibody, allows the detection of at least 0.2 - 0.4 ng/well of recombinant Murine TNF-α. Western Blot: To detect Murine TNF-α by Western Blot analysis this antibody can be used at a concentration of 0.1-0.2 µg/ml. When used in conjunction with compatible secondary reagents, the detection limit for recombinant Murine TNF-α is 1.5-3.0 ng/lane, under either reducing or non-reducing conditions. Note: Additional applications tested on a lot-to-lot basis. Please contact Technical Support for more information. crossreactivity: Mouse, Mouse + Bacteria References SDS CoA Search Product Line Country Of Origin: USA Not for human use. Research Interest COVID-19 AIDS/HIV Angiogenesis/Cardiovascular Apoptosis Cancer Diabetes/Weight Regulation Immune System Inflammation Neurobiology Stem Cells & Differentiation TNF Superfamily Allergy Transplantation product.subtitle.recentcitations First Author Tayabali, A F Title Comparison of the virulence potential of Acinetobacter strains from clinical and environmental sources. Citation PLoS ONE; 7(5) pge37024 PubMed Id 22655033 First Author Cesaro, A Title An inflammation loop orchestrated by S100A9 and calprotectin is critical for development of arthritis. Citation PLoS ONE; 7(9) pge45478 PubMed Id 23029038 First Author Cabilly, Y Title Poor cerebral inflammatory response in eIF2B knock-in mice: implications for the aetiology of vanishing white matter disease. Citation PLoS ONE; 7(10) pge46715 PubMed Id 23056417