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CompareControl Standard Endotoxin for Kinetic-QCL™ Kinetic Chromogenic LAL, E. coli Strain O55:B5Catalog #: E50-643Sales unit: each -
CompareNK – Human Natural Killer Cells, 5 MillionCatalog #: 2W-502Human Natural Killer Cells pos selection, ≥5 million cellsSales unit: each
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CompareNK - Human Natural Killer Cells, Cryopreserved, Negative Selection, 5 MillionCatalog #: 2W-501
Crypreserved ampule of Peripheral Blood Human Natural Killer Cells (CD56 negative immunomagnetic selection) containing ≥ 5 million cells
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Compare100 L Platinum UltraPAKTM Bag, 5/caseCatalog #: 08-E314
100 L Platinum UltraPAKTM Bag
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Compare20 L Platinum UltraPAKTM Bioprocess container, 20/caseCatalog #: 08-E1325
20 L Platinum UltraPAKTM Bioprocess container
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Compare10 L Platinum UltraPAKTM Bag, 20/CaseCatalog #: 08-E1324
10 L Platinum UltraPAKTM Bag
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Compare1 L Platinum UltraPAKTM, 25/caseCatalog #: 08-E1322
1 L Platinum UltraPAKTM Bag
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Compare5 L Platinum UltraPAKTM Bag, 20/CaseCatalog #: 08-E1323
5 L Platinum UltraPAKTM Bag
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ComparePlatinum UltraPAKTM 5 L, 3 ports, 20/caseCatalog #: 08-E210
Platinum UltraPAKTM 5 L, 3 ports
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CompareNebula® Absorbance ReaderCatalog #: 25-365SThe Nebula® Absorbance Reader is a 96-well microplate reader that brings new and improved technology to the laboratory and is optimized to work with WinKQCL® Endotoxin Detection and Analysis Software and our traditional LAL assays such as the PYROGENT® 5000 Kinetic Turbidimetric Assay and the Kinetic-QCL® Kinetic Chromogenic AssaySales unit: each
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Instructions - QCL-1000™ Assay (English)Detailed instructions for performing the QCL-1000™ Endpoint Chromogenic LAL Assay
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PYROSTAR™ ES-F Series BrochureThe PYROSTAR™ ES-F series of reagents are endotoxin-specific and unreactive to β-D-Glucan
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QCL-1000™ Endpoint Chromogenic LAL Assay - Technical TipsThe Importance of Glass Tubes /The Problem with PlasticIncubation Method96-well Plates1 EU/ml Standard PreparationVortexing and Mixing Potential Endotoxin Contaminants
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Instructions – Water for Cell CultureData sheet WFI
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Troubleshooting Guide - Testing Oil Solutions with PYROGENT® Gel Clot LAL AssayEndotoxins, due to their lipid character, tend to remain associated with oils and do not readily enter the aqueous phase of water-oil mixtures. This Tech Tip describes the use of a dispersing agent, PYROSPERSE®, to allow for dissociation of the endotoxin from the oils and for subsequent detection of endotoxin in the aqueous phase by the PYROGENT® Gel Clot LAL Assay.
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Troubleshooting Guide - Endpoint Chromogenic LAL Assay Procedure (English)This is a step-by-step guide depicting how to perform the endpoint chromogenic LAL assay in a 96-well plate.
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Instructions - MycoZap™ Mycoplasma Elimination ReagentMycoZap™ Mycoplasma Elimination Reagent Instructions
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Endpoint Chromogenic Limulus Amebocyte Lysate (LAL) Assay Procedure Quick GuideThis is a step-by-step guide depicting how to perform the endpoint chromogenic LAL assay in a 96-well plate. (English)
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Overcoming Assay Inhibition or Enhancement Technical TipsOne of the most time-consuming aspects of endotoxin testing using Limulus Amebocyte Lysate (LAL) is pretreating samples to overcome assay inhibition and enhancement. All assays, independent of methodology, are standardized using endotoxin in water. Lonza offers three solutions for overcoming LAL testing inhibitions
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White-Paper LAL-vs-rFCLonza discusses the transistion From LAL to rFC Assays
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