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Cytoskeleton/NEW SUMOylation 1 Affinity Beads/3 x 400 ul/ASM11-beads
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Details As part of the Signal-Seeker™ product line, SUMOylation 1 affinity beads have been optimized in order to detect endogenous levels of SUMO1 modified proteins, which often represent <1% of the target protein. SUMOylation 1 affinity beads comprise an anti-SUMO1 antibody (Clone 7A1A2) that has been chemically conjugated to Protein G beads. Validation studies done in HAP1 wildtype and SUMO1 knockout cells have shown that these beads can immunoprecipitate a wide range of SUMO 2/3 modified proteins without detectable leaching of either heavy or light chains in an IP assay. A comprehensive Signal-Seeker™ SUMOylation 2/3 Detection Kit is also available (BK162) and is recommended for first time users.Validation Data: see datasheetEach lot of affinity-bead is quality controlled to provide high batch to batch consistency, see COA documents. Validated Applications Immunoprecipitating total SUMO1 profiles using the Signal-Seeker™ SUMOylation 1 Affinity Beads 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 Affinity Beads compared to older SUMO1 toolsHAP1 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 (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-rabbit-HRP 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.Amount:Each package contains enough SUMOylation 1 beads for 30 reactions. For more information contact: signalseeker@cytoskeleton.comAssociated Products:Signal-Seeker™ SUMOylation 1 Detection Kit (Cat. # BK165)Signal-Seeker™ SUMOylation 2/3 Detection Kit (Cat. # BK162)Signal-Seeker™ Ubiquitination Detection Kit (Cat. # BK161)Signal-Seeker™ Phosphotyrosine Detection Kit (Cat. # BK160)Signal-Seeker™: BlastR™ Rapid Lysate Prep Kit (Cat. # BLR01)Signal-Seeker™: PTMtrue™ SUMOylation 1 Antibody (Cat.# ASM01)AboutFor product Datasheets and MSDSs please click on the PDF links below.Click on the pdf icon below to download the datasheet Certificate of Analysis: available upon requestCitationsNew 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。
如果您想从市场上购买到特定产品,请随时与我们联系。我们在这里为您提供帮助。
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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