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A protein cross-linking probe designed to be used with MS; contains two symmetric collision-induced dissociation-cleavable sites that allow effective identification of DSSO-cross-linked peptides based on their distinct fragmentation patterns
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VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Apoquel Chewable (oclacitinib chewable tablet) is an oral chewable tablet that works differently from other skin allergy medications for dogs. It goes straight to the source to help relieve itch and inflammation at its core. Provides rapid relief from allergic dermatitis and has demonstrated to control allergic pruritus within 24 hours. Addresses the underlying cause of irritation and soothes allergic reactions For dogs older than 12 months of age to help lessen itch and inflammation due to allergic dermatitis Ideal for both short- or long-term treatment and can help to offer relief without many of the side effects associated with other medications
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MF: C4 H4 N O6 S . Na, MW: 217.13, Alternative Names: Sulfo NHS; Hydroxy-2,5-dioxopyrrolidine-3-sulfonicacid; S-NHS. N-hydroxysulfosuccinimide (Sulfo-NHS) is used in conjunction with EDC-HCl (EDAC-HCl) to convert carboxyl groups to Sulfo-NHS esters which react with primary amines.
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Rosmarinic acid is a naturally-occurring phenolic compound with antioxidant and anti-inflammatory properties. This compound inhibits lipid peroxidation of rat liver microsomes by 90% at a concentration of 25 UG/ml.{4778} Rosmarinic acid suppresses endotoxin-induced activation of complement and concomitant formation of prostacyclin.{4407,4408} Formation of 5-HETE and LTB4 from human PMNL is inhibited by rosmarinic acid at concentrations of 10-5 to 10-3 M.{4706}
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Fmoc-Val-Ala-PAB-OH is a protease-cleavable linker used in the synthesis of antibody-drug conjugates. It combines an Fmoc-protected Val-Ala dipeptide with a para-aminobenzyl spacer and a free carboxyl group to enable coupling and self-immolative payload release. Supplied as a high-purity solid, it includes documented solubility and storage guidelines for research use.
PEG4-SPDP is a PEGylated, disulfide-cleavable SPDP linker used to construct antibody-drug conjugates (ADCs). It provides a PEG4 spacer to improve solubility and linker flexibility, and is designed to release payloads under reductive intracellular conditions.
Cleavable disulfide linker for intracellular payload release.
PEG4 spacer improves solubility and linker flexibility.
High purity supplied (~98.0%).
Suitable for antibody-drug conjugation and bioconjugation workflows.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More