
Catalog No.: 101241
Net Contents: 100mg AggRecetin (Ristocetin)
AGGRECETIN® 100mg Ristocetin A Sulfate
AggRecetin® (Ristocetin) Reagent: Peak Platelet Precision with Over 90% Ristocetin Purity for Trusted RIPA Testing
AggRecetin® (Ristocetin) Reagent is intended for use in performing routine Ristocetin-Induced Platelet Aggregation (RIPA) testing on Platelet-Rich Plasma (PRP) samples to assess platelet function.
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Optimized for RIPA Testing: Delivers reliable platelet aggregation results at both low and high Ristocetin concentrations.
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Low-Dose RIPA Sensitivity: Facilitates detection of hyper-responsiveness in type 2B vWD and PT-vWD patients.
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High-Dose RIPA Confirmation: Verifies normal platelet-vWF interaction or rules out qualitative defects in vWF.
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Supports Targeted Guidelines: Aligns with international guidelines for vWD classification and platelet function evaluation.
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Enables GPIb-vWF Binding Assessment: Reveals abnormalities in platelet receptor binding activity central to vWD pathology.
AggRecetin® (Ristocetin) Reagent is manufactured for precision in Ristocetin-Induced Platelet Aggregation (RIPA) testing, a critical assay in the evaluation of von Willebrand Disease (vWD). With a concentration exceeding 90% pure Ristocetin, AggRecetin ensures consistent and reliable platelet aggregation responses, delivering the confidence laboratories need for both screening and confirmation stages. This high-purity formulation minimizes variability and supports accurate interpretation of platelet-von Willebrand factor (vWF) interactions.
Designed to perform across a range of concentrations, AggRecetin is ideal for both low-dose and high-dose RIPA testing protocols. Low-dose RIPA testing is particularly sensitive for detecting hyper-responsiveness in patients with type 2B vWD and platelet-type vWD (PT-vWD), enabling early and precise identification of these subtypes. High-dose RIPA serves as a valuable confirmatory step, distinguishing between normal platelet function and potential qualitative abnormalities in vWF. This dual utility enhances confidence and helps guide appropriate clinical management.
AggRecetin plays a vital role in the evaluation workup of patients with suspected vWD, particularly when used within a comprehensive testing guidelines. Its use aligns with internationally recognized guidelines, making it a trusted component in the stratification and classification of vWD subtypes. By supporting a structured evaluation pathway, AggRecetin helps laboratories streamline workflows while upholding the highest standards of clinical accuracy.
Beyond classification, AggRecetin enables precise functional assessment of the GPIb-vWF interaction, a critical step in platelet adhesion. Abnormalities in this interaction are central to the pathophysiology of vWD, especially in type 2B and PT-vWD, where enhanced binding leads to abnormal platelet clumping. With AggRecetin, laboratories gain a powerful tool to explore these mechanisms, strengthening their evaluation capabilities and ensuring the most informed patient care decisions.
Kindly explore the materials provided on this page, including the AggRecetin Reagent Product Data Sheet and Routine Agonist Expected Results Chart. Additionally, refer to the and the AggRecetin Instruction for Use (IFU) and the AggRecetin Safety Data Sheet (SDS), available in six languages. For our European and United Kingdom customers and distributors, carefully review the AggRecetin EU Declaration of Conformity and the AggRecetin UK Declaration of Conformity to ensure compliance and tailored understanding for these specific regions. This information is crucial for gaining a comprehensive understanding of the product details and specifications.