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PROTEIN A/G MAGNETIC IP-MS KIT EACH,90409,赛默飞世尔

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订货号 9SE4682
品牌型号 赛默飞世尔 90409
货期 询货期
最小订货量 1套
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产品介绍 Product Description
规格
Detection Method: Mass Spectrometry
Final Product Type: Protein
For Use With (Equipment): KingFisher™ Flex, Magnetic Stand
Product Line: Pierce™
Starting Material: Protein samples, Cell Lysate
Workflow Step: Sample Enrichment
储存
Protein A/G Magnetic Beads, 1 mL
IP-MS Cell Lysis Buffer, 100 mL
IP-MS Wash Buffer A, 75 mL
IP-MS Wash Buffer B, 40 mL
IP-MS Elution Buffer, 6 mL
MgCl2 (1 M), 0.75 mL

Store in refrigerator (2–8°C).
描述

The Thermo Scientific™ Pierce™ MS-Compatible Magnetic IP Kit (Protein A/G) provides mass spectrometry-friendly reagents and an optimized protocol to enable highly effective and efficient immunoprecipitation and co-immunoprecipitation of target antigens upstream of LC-MS analysis.

MS-compatible—reagents directly compatible with in-solution peptide digestion, enriched samples contain minimal detergent residuals detected using LC-MS
Sensitive—procedure successfully enriches low abundance proteins (low ng range)
Low background—binding, wash, and elution buffers optimized to minimize enrichment of background proteins
Robust—procedure and reagents have been robustly tested with numerous targets to ensure consistent enrichment of low abundance proteins (ng range) with at least 2 peptides identified per protein

The Pierce MS-Compatible Magnetic IP Kit (Protein A/G) uses high-quality Pierce Protein A/G Magnetic Beads to provide wider flexibility of antibody capture than either Protein A or G alone. The optimized kit components have been formulated to be compatible with downstream LC-MS analysis. After the immunoprecipitation procedure, the target-enriched elution fraction is ready for in-solution tryptic digestion without the need for gel purification, detergent removal, or desalting.

This kit has been rigorously validated using numerous target antigens with varying expression levels, including targets previously undetected without enrichment or by western blotting. Additionally, the reagents and procedures have been validated using both manual and automated magnetic separation.

Applications:
• Enrichment of low abundance targets to improve MS sensitivity
• Identification of target proteins that are not detectable by western blotting
• Quantitation of target proteins by LC-MS analysis
• Screening of antibodies for IP-MS
• Enrichment of target proteins upstream of targeted analysis (SRM)

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