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Cytoskeleton/NEW Signal-Seeker™ SUMOylation 1 Detection Kit (30 assay)/30 assays/BK165
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Details The Signal-Seeker™ line of produts have been developed to allow simple analysis of key regulatory protein modifications by specialists and non-specialists alike. The comprehensive Signal-Seeker™ kits provide an affinity bead system to isolate and enrich modified proteins from any given cell or tissue lysate. The enriched protein population is then analyzed by standard western blot procedures using a primary antibody to the target protein. Product Uses IncludeInvestigate transient regulatory mechanisms Measure signalling events of multiple pathway member proteins Discover new modifications of your protein of interest Gain insight into regulatory mechanisms Measure endogenous or transiently expressed protein signalling events Validation Data: see datasheetKit contentsThe SUMOylation 1 kit contains the following components:Lysis and protein quantitation stepIP and pre-clear stepWash stepElution stepWestern step BlastR™ Lysis Buffer BlastR™ Dilution Buffer BlastR™ Filters Protease Inhibitor Cocktail De-SUMOylation inhibitor Cocktail Precision Red™ Protein Assay Reagent SUMOylation 1 Affinity Beads IP Control Beads BlastR™ Wash Buffer Spin Columns Bead Elution Buffer Chemiluminescent Reagent A Chemiluminescent Reagent B Anti-SUMO1 antibody Example resultsThere are many applications for these kits, here we describe an interesting example:Application 1: Investigate significant SUMOylation 1 eventsImmunoprecipitating total SUMO1 profiles using the Signal-Seeker™ SUMOylation 1 Detection Kit compared to older SUMO1 tools(A) HAP1 wildtype (WT) or SUMO1 knockout (KO) lysate, was obtained using BlastR lysis and filter system. 1 mg of each lysate were incubated with 40 µg of each SUMO1 affinity reagent: ASM11-beads (Cytoskeleton), 21C7 (Invitrogen—purified), 21C7 (DSHB—supernatant), D11-beads (Santa Cruz) and conjugated SUMO1 IgG control beads (CIG03). 21C7 antibodies were captured with protein G agarose beads to enrich for SUMO-1 modified proteins. Samples were separated by SDS-PAGE and transferred to PVDF. Enriched SUMO1 samples were analyzed by western blot using ASM01 (Cytoskeleton) antibody at 1:5000, and mouse Trubelot Ultra-HRP secondary at 1:1000 in 5% milk. Trueblot secondary was used to minimize heavy and light chain detection from 21C7 samples. (B): IP was performed using ASM11 as in Fig 1A. SUMO1 modified proteins were visualized with ASM01 1:5000, and anti-mouse secondary at 1:20,000 to highlight the profile of SUMOylated proteins in the region between 64-30 kDa that may be masked by heavy and light chain interference when using unconjugated antibodies for IP.Immunoprecipitating SUMO1 modified target proteins using the Signal-Seeker™ SUMOylation 1 Detection Kit compared to older SUMO1 tools HAP1 wildtype (WT) or SUMO1 knockout (KO) lysate, was obtained using BlastR lysis and filter system. 1 mg of each lysate were incubated with 40 ug of each SUMO1 affinity reagent: ASM11-beads (Cytoskeleton), 21C7 (DSHB—supernatant), and conjugated SUMO1 IgG control beads (CIG03). 21C7 antibodies were captured with protein G agarose beads to enrich for SUMO-1 modified proteins. Samples were separated by SDS-PAGE and transferred to PVDF. Target proteins: (A) TFII-I, RanGAP1, and (B) schmd1 were analyzed for their SUMO1 modified forms by western blot. Anti-rabbitHRP labeled secondary antibody was used at 1:10,000. All three primary antibodies are rabbit polyclonal antibodies, and should not bind heavy and light chain fragments from the IP antibody.Other experiments that could be attempted in this area of research include:• Pharmacological investigation of SUMOylating and de-SUMOylating enzymes involved in regulation of target proteins.• Investigate SUMOylation under a variety of different growth factors or drug treatments.• Examine the interaction of SUMOylated target proteins with its downstream effectors.• Examine crosstalk between SUMOylation 1 and other PTMs for target proteins. For more information contact: signalseeker@cytoskeleton.comAssociated Products:Signal-Seeker™ SUMOylation 2/3 Detection Kit (Cat. # BK162)Signal-Seeker™ Ubiquitination Detection Kit (Cat. # BK161)Signal-Seeker™: BlastR™ Rapid Lysate Prep Kit (Cat. # BLR01)Signal-Seeker™ SUMOylation 2/3 Affinity Beads (Cat.# ASM11-beads)Signal-Seeker™: PTMtrue™ SUMOylation 2/3 Antibody (Cat.# ASM01)About Click on the pdf icon below to download the manual CitationsNew product released in 2018! For the most recent publications citing this and other Signal-Seeker™ products, see our Signal-Seeker™ Validation Data Page click hereFaqsVisit our Signal-Seeker™ Tech Tips and FAQs page for technical tips and frequently asked questions regarding this and other Signal-Seeker™ products click here If you have any questions concerning this product, please contact our Technical Service department at tservice@cytoskeleton.com
Cytoskeleton,Inc.成立于1993年。自成立以来,我们一直在不断扩大产品范围。
Cytoskeleton,Inc.很高兴为药物筛选,信号转导和细胞骨架研究提供广泛的试剂盒和产品。我们专注于纯化蛋白的生产和易于使用的试剂盒,以研究生化和细胞过程。我们的试剂盒既可用于基础研究或小型筛查的少量样品,也可用于大型筛查的高通量规模
除了我们现有的产品外,我们还提供产品系列中微管,微管蛋白,运动蛋白,小G蛋白效应物,GAP,GEF和其他几种蛋白的药物筛选服务。有关更多信息,请参见我们的药物筛选服务页面。
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由于我们的科学家在各自的专业领域都有多年的工作经验,因此我们能够提供高质量的产品。自1993年成立以来,我们以合理的价格生产优质的产品而闻名。
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