Antihistamines or H1 blockers

The RPI L-histidine hydrochloride monohydrate is suitable for use in research facilities and chemical laboratories to conduct wide range of experiments. It is available in sturdy bottle that endures heavy and rigorous usage.

Mixture of four protease inhibitors for inhibiting serine proteases. Supplied in 1ml DMSO. Contains: AEBSF Aprotinin Elastatinal GGACK Specificity: Chymotrypsin Kallikrein Plasmin Thrombin Trypsin Elastase Urokinase Factor Xa

A major drawback of current blocking solutions, such as BSA , casein and milk powder, is that they are derived from animal sources. The presence of animal proteins can often lead to high non-specific backgrounds as antigens and antibodies, generated

An active, deacetylated metabolite of T-2 toxin inhibits protein synthesis and cell proliferation in plants causes acute and chronic toxic effects in animals that ingest contaminated plant materials.

A major metabolite of histamine used as a biomarker of histaminergic system activity.

Cayman&rsquos HDAC1 Inhibitor Screening Assay provides a fast, fluorescence based method for screening HDAC1 inhibitors. The procedure requires only two easy steps, both performed in the same microplate.

An active, deacetylated metabolite of T-2 toxin inhibits protein synthesis and cell proliferation in plants causes acute and chronic toxic effects in animals that ingest contaminated plant materials.

A non-sedating antihistamine that acts as a selective inverse agonist of peripheral histamine H1 receptors (Ki = 35 nM) inhibits the release of LTC4 (IC₅₀ = 8 &microM) and histamine (IC₅₀ = 11 &microM) from rodent mast cells

A snake venom-derived toxin that irreversibly binds nAChRs (Ki = ~ 2.5 &microM in rat) present in skeletal muscle, blocking action of ACh at the postsynaptic membrane and leading to paralysis.

A competitive antagonist of muscarinic (M) receptors (Ki = 1.4, 2.7, 3.6, 3.1, and 2.2 nM for M1 through M5, respectively).

Synonyms: MIBG

A non-sedating antihistamine that acts as a selective inverse agonist of peripheral histamine H1 receptors (Ki = 35 nM) inhibits the release of LTC4 (IC₅₀ = 8 &microM) and histamine (IC₅₀ = 11 &microM) from rodent mast cells