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Showing 1-30 of 797 results for "80307-12-6" within Site Content
F-12 Coon's Modification Formulation
F-12 Coon's Modification Formulation
Revised IFU Method No. 12 for Alicyclobacillus spp.
New microbiological standards for fruit juices focus on detecting Alicyclobacillus spp. using BAT broth and agar.
DMEM/nutrient Mixture F-12 Formulation
Dulbecco's Modified Eagle's Medium/Ham's Nutrient Mixture F-12 (DME/F12) Formulation
Nutrient Mixture F-12 Ham Formulation
Nutrient Mixture F-12 Ham Formulation
Performing a Separation with IgG Sepharose 6 Fast Flow
Perform a separation with IgG Sepharose 6 Fast Flow from Cytiva, an Affinity Chromatography product for purification of recombinant fusion proteins containing a protein A tail.
Enzymatic Activity of Glucose-6-Phosphatase [EC 3.1.3.9]
To measure glucose-6-phosphatase activity, the Taussky-Shorr method is used. This method is a spectrophotometric stop-rate determination assay that is measured at 660 nm.
Ni Sepharose 6 Fast Flow for Protein Purification
Ni Sepharose 6 Fast Flow purifies histidine-tagged proteins efficiently, offering high cross-linked agarose beads with Ni2+ ions.
Oligonucleotide Standard 6 Mix LC-UV Analysis
Chromolith® RP-18e columns optimize Oligo Standard 6 separation with varied flow rates and ion-pairing reagent evaluation.
Update of the IFU Method No. 12 for Alicyclobacillus spp
In this webinar, we discuss the revised IFU method no. 12 for Alicyclobacillus detection in fruit juices, and aseptic filling lines sterility testing.
DMEM/F12 Media
Find DMEM/F-12 modifications for versatile cell culture needs, combining advantages of DMEM and F-12 media.
Enzymatic Assay of Glucose-6-Phosphate Dehydrogenase (EC 1.1.1.49)
To measure glucose-6-phosphate dehydrogenase activity, beta-nicotinamide adenine dinucleotide phosphate is used in a spectrophotometric rate determination assay at 340 nm.
Phorbol 12-myristate 13-acetate Molecular Biology Reagent Protocol
T-cell activation is normally triggered by the interaction of a cell surface receptor to its specific ligand molecule
Greener Alternatives Evaluation Matrix
Green chemicals evaluation aligns with the 12 Principles of Green Chemistry, emphasizing resource efficiency and hazard reduction.
Flavor & Fragrance Demo Kit Request
F&F demo kit #12 offers a variety of products for experience, supporting your research needs.
Dextran
Dextran polymer details: composed mainly of alpha-D-(1-6) linkages with varied branch lengths.
Performing a Separation or Removal of Albumin with HiTrap® Blue HP and Blue Sepharose 6 Fast Flow
This page shows how to separate or remove albumin by affinity chromatography using HiTrap Blue HP and Blue Sepharose 6 Fast Flow.
Enzymatic Assay of Peroxidase (EC 1.11.1.7) 2,2'-Azino-bis(3-Ethylbenzthiazoline-6-Sulfonic Acid) as a Substrate
To standardize a procedure for the assay of Peroxidase using 2,2'-Azino-bis(3-Ethylbenzthiazoline-6-Sulfonic Acid) as a substrate.
Ham’s Nutrient Mixture and Derivatives
Learn about Ham's F-10 and Ham's F12 and their various modifications - including Ham's F-12 with stable glutamine.
ICP-MS Heavy Metals Analysis in Hemp Food
ICP-MS analyzes 12 heavy metals in hemp-containing food samples using standard addition calibration for accurate quantification.
Removal of Albumin Using Blue Sepharose® Chromatography Media
Remove albumin from affinity chromatography samples using HiTrap™ Blue HP or Blue Sepharose® 6 Fast Flow from Cytiva.
Methods of Synthesizing Monodisperse Colloidal Quantum Dots
Colloidal quantum dots (CQDs) are semiconducting crystals of only a few nanometers (ca. 2–12 nm) coated with ligand/surfactant molecules to help prevent agglomeration.
Enzymatic Assay of Alcohol Oxidase (EC 1.1.3.13)
To measure alcohol oxidase activity, this assay uses 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) and a continuous spectrophotometric rate determination at 405 nm.
Determination of Hydrocortisone from Topical Cream Using Discovery DSC-Si SPE and Reversed-Phase HPLC-UV
Using the method described in this report, an average absolute recovery and RSD value of 99.86 ± 6.99% (n=6) was observed, to determine an average of 1.02% hydrocortisone in topical cream.
Purification or Removal of DNA-Binding Proteins
This page shows how to purify or remove DNA-binding proteins with Heparin Sepharose High Performance, Heparin Sepharose 6 Fast Flow, Capto Heparin from Cytiva.
UHPLC Analysis of Nucleosides on Supel™ Carbon LC Column: Performance Comparisons with Competitor
Ultra-high performance liquid chromatographic (UHPLC) separation of 12 nucleosides using Supel™ Carbon LC column in 15 minutes for use in identification and quantitation of nucleoside biomarkers.
USDA FSIS STEC Guidance Implementation
Discover the expanded USDA FSIS verification testing for the 'Big 6' non-O157 STEC in beef products and explore accurate testing solutions and industry practices for enhanced food safety.
DOZN™ Quantitative Green Chemistry Evaluator
Quantify the greenness of any product or process using the DOZN™ green chemistry tool, which uses the 12 Principles of Green Chemistry to evaluate chemicals, synthetic routes, and chemical processes.
Determination of Water Content in Phenol Using Karl Fischer Titration
Accurately measure the moisture content in Phenol (C6H5OH) through Karl Fischer titration, using both Volumetric and Coulometric methods.
Purification of Histidine-Tagged Recombinant Proteins Using Ni Sepharose® High Performance
Ni Sepharose High Performance consists of highly cross-linked 6% agarose beads (34 µm) to which a chelating group has been immobilized and subsequently charged with Ni2+ ions.
Preservation of Moisture-Sensitive Chemical Reagents
Preserve reagent quality of air- and moisture-sensitive reagents using nitrogen or argon in crown-cap bottles with a 6 mm diameter hole in the crown-cap and a PTFE-faced rubber liner.
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