Procurou por: FUJIFILM+WAKO+CHEMICALS

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αBET™ CMD Rapid Endotoxin Detection System

Fornecedor: FUJIFILM WAKO CHEMICALS

Descrição: The CMD αBET™ system is a fully integrated testing system that provides a rapid and sustainable solution to endotoxin testing without compromising on sensitivity or performance. Using our FDA-licensed turbidimetric Limulus amebocyte lysate (LAL) reagent, quantitative results are provided in under half the time of other testing formats, with less reagent consumption and minimal user input.

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Limulus Color Ky Test

Código de Artigo: (WAKF291-53101)

Fornecedor: FUJIFILM WAKO CHEMICALS

Descrição: The Limulus Color KY Series are quantitative kinetic chromogenic assays (KCA) that are endotoxin-specific and unreactive to (1→3)-β-D-glucan. This series includes both a multi-test kit and a single-test kit, which utilise a synthetic substrate that produces a yellow color to detect endotoxin with high sensitivity.

UOM: 1 * 60 unid.

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Accessories for Endotoxin Tests

Fornecedor: FUJIFILM WAKO CHEMICALS

Descrição: LAL Reagent Water can be used to fulfill all aspects of endotoxin testing. From reconstitution of both the CSE and LAL for the creation of standard curves to the making of product dilutions, LAL reagent water provides reliable and reproducible data when paired with our endotoxin-specific LAL reagents.

Limulus Color Ky Single Test

Código de Artigo: (WAKF291-53601)

Fornecedor: FUJIFILM WAKO CHEMICALS

Descrição: The Limulus Color KY Series are quantitative kinetic chromogenic assays (KCA) that are endotoxin-specific and unreactive to (1→3)-β-D-glucan. This series includes both a multi-test kit and a single-test kit, which utilize a synthetic substrate that produces a yellow color to detect endotoxin with high sensitivity.

UOM: 1 * 25 unid.

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Toximaster® QC8 software

Fornecedor: FUJIFILM WAKO CHEMICALS

Descrição: The Toximaster® QC8 software supports data processing based on the protocols complying with three types of pharmacopeia (USP, EP, JP) for bacterial endotoxin testing. This software is compliant with FDA 21 CFR Part 11 ERES (electronic records/electronic signature), which requires the proper information from all parties involved in the testing of the sample.