Protein Mass Spectrometry Sample Prep
Thermo Scientific™ Pierce™ 6 Protein Digest, equimolar, LC-MS grade
Calibrate and maintain quality control for mass spectrometry (MS) analysis of proteomic samples using the Thermo Scientific™ Pierce™ 6 Protein Digest Standard, Equimolar, LC-MS Grade, a highly validated equimolar protein digest mixture.
Thermo Scientific™ Pierce™ Triple Quadrupole Calibration Solution
Calibrate Triple Stage Quadrupole (TSQ) mass spectrometers using a mixture of high purity, ionizable components specifically designed for positive mode calibration.
Promega 6 x 5 LC-MS/MS Peptide Reference Mix
The 6 x 5 LC-MS/MS Peptide Reference Mix is a unique reagent designed to monitor liquid chromatography (LC) and mass spectrometry (MS) instrument performance and assist in method development and optimization.
Thermo Scientific™ Pierce™ MS-Compatible Magnetic IP Kits
Achieve highly efficient, compatible immunoprecipitation and co-immunoprecipitation of target antigens for downstream LC-MS analysis using Thermo Scientific Pierce MS-Compatible Magnetic IP Kits with streptavidin or Protein A/G magnetic beads.
Thermo Scientific™ High Select™ Depletion Spin Columns
Decrease albumin, immunoglobulins, and other high-abundance proteins from human serum or plasma in preparation for mass spectrometry analysis, or 1D and 2D gel electrophoresis using High Select depletion spin columns or resin.
Cytiva HiTrap™ IMAC Columns
For optimizing purification of histidine-tagged proteins when Ni +2 is not the best choice of metal ion
Thermo Scientific™ Pierce™ C18 Spin Tips & Columns
Thermo Scientific Pierce C18 Spin Columns (10–150 μL) and Spin Tips (10–100 μL) effectively remove interfering contaminants, while also maintaining excellent binding and recovery of peptide samples for use upstream of mass spectrometry and other high sensitivity detection methods.
Cayman Chemical Sp-5 6-dIchloro-cBIMPsodIu 1mg
A potent activator of PKA (Ki = 30 nM) that is selective for PKA over PKG (Ki = 10 µM); resistant to degradation by cyclic nucleotide phosphodiesterases, displays good cell permeability, and prevents the aggregation of platelets stimulated with thrombin
Cayman Chemical Sp-5 6-dIchloro-cBIMPsodIu 5mg
A potent activator of PKA (Ki = 30 nM) that is selective for PKA over PKG (Ki = 10 µM); resistant to degradation by cyclic nucleotide phosphodiesterases, displays good cell permeability, and prevents the aggregation of platelets stimulated with thrombin
Biotium Spastin(Sp 6C6), CF488A conjugate, 0.1mg/mL
The AAA protein family members share an ATPase domain and have roles in various cellular processes including intracellular motility, membrane trafficking, proteolysis, protein folding and organelle biogenesis. Spastin, a member of the AAA protein family, is a 616 amino acid protein and is involved in the function or assembly of nuclear protein complexes. The Spastin protein is expressed ubiquitously and localizes to the nucleus and the cytoplasm, where it may also be involved in microtubule dynamics. Mutations in the Spastin gene (SPAST, SPG4) cause the most common form of spastic paraplegia 4, an autosomal dominant form of hereditary spastic paraplegia (HSP). HSPs comprise a group of inherited neurological disorders characterized by spastic lower extremity weakness due to a length-dependent, retrograde axonopathy of corticospinal motor neurons. SPAST-specific mutations account for approximately 40% of all autosomal dominant HSPs. Primary antibodies are available purified, or
Biotium Spastin(Sp 6C6), CF488A conjugate, 0.1mg/mL
The AAA protein family members share an ATPase domain and have roles in various cellular processes including intracellular motility, membrane trafficking, proteolysis, protein folding and organelle biogenesis. Spastin, a member of the AAA protein family, is a 616 amino acid protein and is involved in the function or assembly of nuclear protein complexes. The Spastin protein is expressed ubiquitously and localizes to the nucleus and the cytoplasm, where it may also be involved in microtubule dynamics. Mutations in the Spastin gene (SPAST, SPG4) cause the most common form of spastic paraplegia 4, an autosomal dominant form of hereditary spastic paraplegia (HSP). HSPs comprise a group of inherited neurological disorders characterized by spastic lower extremity weakness due to a length-dependent, retrograde axonopathy of corticospinal motor neurons. SPAST-specific mutations account for approximately 40% of all autosomal dominant HSPs. Primary antibodies are available purified, or