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Multiple affinity removal system columns

Manufactured by Agilent Technologies
Sourced in United States

The Agilent Multiple Affinity Removal System (MARS) columns are designed to remove high-abundance proteins from complex biological samples, such as plasma or serum. The columns use affinity-based chromatography to selectively remove the most abundant proteins, allowing for the detection and analysis of low-abundance proteins that may be of interest for research or diagnostic purposes.

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2 protocols using multiple affinity removal system columns

1

Quantitative Proteomic Sample Preparation

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Iodoacetamide (IAA), tris(2-carboxyethyl) phosphine hydrochloride (TCEP), triethylammonium hydrogen carbonate buffer (TEAB) 1M pH = 8.5, sodium dodecyl sulfate (SDS), and LACB from bovine milk were purchased from Sigma (St. Louis, MO, USA). Formic acid (FA, 99%) was from BDH (VWR International Ltd., Poole, UK). Hydroxylamine solution 50 wt% in H2O (99.999%) was acquired from Aldrich (Milwaukee, WI, USA). Water (18.2 MΩ·cm at 25 °C) was obtained from a Milli-Q apparatus (Millipore, Billerica, MA, USA) and acetonitrile from BDH. Trifluoroacetic acid Uvasol® was sourced from Merck Millipore (Billerica, MA, USA). The sixplex tandem mass tags (TMTs) were purchased from Thermo Scientific (Rockford, IL, USA). Sequencing grade-modified trypsin was procured from Promega (Madison, WI, USA). For immuno-affinity depletion of 14 abundant human proteins, multiple affinity removal system (MARS) columns, Buffer A, and Buffer B were obtained from Agilent Technologies (Wilmington, DE, USA). Oasis HLB cartridges (1cc, 30 mg) were acquired from Waters (Milford, MA, USA) and strong cation-exchange (SCX) solid-phase extraction (SPE) cartridges from Phenomenex (Torrance, CA, USA).
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2

Quantitative Proteomics with TMT Labeling

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Iodoacetamide (IAA), tris(2‐carboxyethyl) phosphine hydrochloride (TCEP), triethylammonium hydrogen carbonate buffer 1 M pH 8.5, sodium dodecyl sulfate, and β‐lactoglobulin (LACB) from bovine milk were purchased from Sigma (St. Louis, MO, USA). Formic acid (FA, 99%) and CH3CN were from BDH (VWR International Ltd., Poole, UK). Hydroxylamine solution 50 wt% in H2O (99.999%) was acquired from Aldrich (Milwaukee, WI, USA). H2O (18.2 MΩ cm at 25°C) was obtained from a Milli‐Q apparatus (Millipore, Billerica, MA, USA). Trifluoroacetic acid Uvasol was sourced from Merck Millipore (Billerica, MA, USA). The 6‐plex isobaric tandem mass tags (TMTs) were purchased from Thermo Scientific (Rockford, IL, USA). Sequencing grade modified Lys‐C/trypsin was procured from Promega (Madison, WI, USA). For immuno‐affinity depletion of 14 abundant human proteins, multiple affinity removal system (MARS) columns, Buffer A, and Buffer B were obtained from Agilent Technologies (Wilmington, DE, USA). Oasis HLB cartridges (1cc, 30 mg) were acquired from Waters (Milford, MA, USA) and Strata‐X 33u Polymeric reversed‐phase (RP) and Strata‐X‐C 33u Polymeric strong cation‐exchange (SCX) solid‐phase extraction (SPE) cartridges (30 mg/1 mL) from Phenomenex (Torrance, CA, USA).
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