Protease Inhibitors and Phosphatase Inhibitors
Thermo Scientific™ Pierce Protease Inhibitor Tablets
Thermo Scientific™ Pierce Protease Inhibitor Tablets are broad-spectrum protease inhibitors that are highly effective at preventing proteolytic degradation for cell lysis and protein extraction experiments
Thermo Scientific™ Halt™ Protease and Phosphatase Inhibitor Cocktails
Prevent protein degradation and stabilize phosphorylation with this all-in-one cocktail of protease and phosphatase inhibitors.
Thermo Scientific™ Halt™ Protease Inhibitor Cocktails
Inhibit proteolytic degradation during cell lysis and protein extraction with these ready-to-use concentrated stock solutions of protease inhibitors.
Thermo Scientific™ Pierce Protease Inhibitor Mini Tablets
Thermo Scientific™ Pierce Protease Inhibitor Mini Tablets are broad-spectrum protease inhibitors that are highly effective at preventing proteolytic degradation for cell lysis and protein extraction experiments
Thermo Scientific™ Halt™ Phosphatase Inhibitor Cocktail
Stabilize serine, threonine and tyrosine phosphorylation of proteins in cells and tissues with this cocktail of phosphatase inhibitors.
Thermo Scientific™ Pierce Protease and Phosphatase Inhibitor Mini Tablets
Thermo Scientific™ Pierce Protease and Phosphatase Inhibitor Mini Tablets broad-spectrum protease and pghospahatase inhibitor formulation provides complete protection from dephosphorylation and proteolytic degradation.
Thermo Scientific™ Pierce Phosphatase Inhibitor Mini Tablets
Thermo Scientific™ Pierce Phosphatase Inhibitor Mini Tablets provide complete cell lysate and biological sample protection from dephosphorylation with a broad spectrum phosphatase inhibitor formulation.
Thermo Scientific™ Pierce™ Protease Inhibitor Tablets
Thermo Scientific™ Pierce Protease Inhibitor Tablets and Mini Tablets are broad-spectrum protease inhibitors that are highly effective at preventing proteolytic degradation for cell lysis and protein extraction experiments.
Invitrogen™ Novex™ AcTEV™ Protease
Specifically recognizes a seven amino acid sequence (Glu-Asn-Leu-Tyr-Phe-Gln-Gly, cleaving between Gln and Gly), ideal for removing affinity tags from fusion proteins
EMD Millipore™ Calbiochem™ N-Ethylmaleimide
Sulfhydryl alkylating reagent that inhibits H+-ATPase and suppresses the short circuit current (IC50 = 22 μM) in pancreatic duct cells.
Thermo Scientific™ Protease Inhibitor Cocktails
Protect your sample from proteolytic degradation during cell lysis with these broad-spectrum protease inhibitor cocktails.
Thermo Scientific™ Pierce™ Protease Inhibitors
Customize your protease inhibitor cocktail formulation with these small packages of individual protease inhibitor peptides and compounds.
EMD Millipore™ Calbiochem™ Fucosyltransferase Inhibitor, 2F-Peracetyl-Fucose
2F-Peracetyl-Fucose is a cell-permeable fluorinated fucose derivative that acts as an inhibitor of fucosyltransferases following its uptake and metabolic transformation into a GDP-fucose mimetic.
Invitrogen™ Novex™ SUMO Protease
A recombinant fragment of ULP1 (Ubl-specific protease 1) from Saccharomyces cerevisiae
EMD Millipore™ Calbiochem™ Protease Inhibitor Cocktail Set V, EDTA-Free
A cocktail of four protease inhibitors for the inhibition of serine, cysteine, but not metalloproteases.
EMD Millipore™ Calbiochem™ Protease Inhibitor Cocktail Set III, EDTA-Free
Protease inhibitor cocktail III, EDTA-free for inhibiting aspartic, cysteine, and serine proteases as well as aminopeptidases in mammalian cells and tissues.
EMD Millipore™ Calbiochem™ Smoothened Agonist, SAG
A cell-permeable Smoothened Agonist, SAG, CAS 364590-63-6, modulates the coupling of Smo with its downstream effector by interacting with the Smo heptahelical domain (KD = 59 nM).
EMD Millipore™ Calbiochem™ Beclin-1 Activator II, retro-inverso TAT-Beclin-1
A cell-permeable, all-D-amino acid autophagy-inducing peptide.
EMD Millipore™ Calbiochem™ Protease Inhibitor Cocktail Set I
A cocktail of five protease inhibitors that will inhibit a broad range of proteases and esterases. Supplied with a data sheet.
EMD Millipore™ Calbiochem™ InSolution™ γ-Secretase Inhibitor X
InSolution™ γ-Secretase Inhibitor X is a 1 mM solution in DMSO. A highly potent inhibitor of g-secretase (IC50 = 17, 48, 67 nM for Aβtotal, Aβ40 & Aβ42 in SHSY5Y cells overexpressing spβA4CTF).
Promega™ Protease Inhibitor Cocktail
A mixture of six different protease inhibitors with different target protease specificities
EMD Millipore™ Calbiochem™ Phosphatase Inhibitor Cocktail Set II
A cocktail of five phosphatase inhibitors for the inhibition of acid and alkaline phosphatases as well as protein tyrosine phosphatases (PTPs). Suitable for use with cell lysates and tissue extracts.
EMD Millipore™ Calbiochem™ InSolution™ Y-27632
Y-27632A, CAS 146986-50-7, is a cell-permeable, reversible, inhibitor of Rho kinases (Ki = 140 nM for p160ROCK). Enhances survival & cloning efficiency of ESC without affecting their pluripotency.
EMD Millipore™ Calbiochem™ Adenosine 3′,5′-cyclic Monophosphate, N6,O2′-Dibutyryl-, Sodium Salt
This Dibutyryl-cAMP, CAS 16980-89-5, is a cell-permeable cAMP analog that preferentially activates PKA.
EMD Millipore™ Calbiochem™ Plasminogen Activator Inhibitor-1, Mutant, Human, Recombinant
Primarily used for Protease Inhibitors applications.
EMD Millipore™ Calbiochem™ Beclin-1 Activator I, TAT-Beclin-1, Scrambled
A randomly shuffled Beclin-1 (267-284) peptide made cell-permeable by covalently attaching to HIV-1 Tat protein transduction domain via a diglycine linker
EMD Millipore™ Calbiochem™ InSolution™ TAPI-2
A 10 mM (1 mg/241 μL) sterile-filtered solution of TAPI-2 in H2O.
EMD Millipore™ Calbiochem™ PPACK, Dihydrochloride
PPACK, Dihydrochloride, CAS 142036-63-3, is an extremely potent and selective irreversible inhibitor of thrombin (Kobs/[I] = 107M−1S−1). Reacts with thrombin in a 1:1 stoichiometry.
EMD Millipore™ Calbiochem™ Cathepsin D/E Substrate, Fluorogenic
An internally quenched fluorogenic 11-mer peptide that acts as a sensitive and selective substrate for cathepsins D and E, but not cathepsins B, H, or L .
EMD Millipore™ Calbiochem™ STING Agonist, 2ʹ3ʹ-cGAMP
A cyclic-dinucleotide (cyclic-GMP-AMP) based compound that binds to the C-terminal domain of adaptor endoplasmic reticulum protein known as STING with high affinity (Kd = 4nM) and induces the synthesis of interferon-b (IFN-b) in mammalian cells (EC50 =