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A Simple Spectrophotometric Method for the Determination Of
J Clin Pathol: first published as 10.1136/jcp.14.2.202 on 1 March 1961. Downloaded from 202 Technical methods usual laboratory filters may give falsely increased values.) Of the clear and colourless filtrate 10 ml. is pipetted into A a 25 ml. measuring flask and 10 ml. reagent (3) added. simple spectrophotometric After mixing dilute with distilled water to the mark and method for the determination of renew mixing. After 10 minutes the mixture is ready for reading. The colour is stable, according to Watt and urea in blood and urine Chrisp, for 11 days. READING T. K. WITH, TOVE DREYER PETERSEN, AND BIRGIT PETERSEN From the Central Laboratory, Svend- The reactions are read in a spectrophotometer at 420 nm. borg County Hospital, Denmark with a blank prepared in the same way as the reaction mixture but with 3 ml. of distilled water instead of 3 ml. of blood. The urea standard (reagent 4) is treated in the Several methods for urea in determining blood and urine same way as the blood. Cuvettes of 1 cm. thickness are are in use in clinical laboratories, but none is ideal in suitable. mass routine The analysis. spectrophotometric method If p, s, and b are the extinctions of the the based on a modified Ehrlich sample, reagent proposed by Watt standard, and the blank respectively, the urea concen- and Chrisp (1954) for pure solutions is therefore of tration is interest because it can be modified for use in mass clinical analyses of blood and urine. Brown (1959) has l00(p-b)/(s-b) mg./100 ml. -
Autoclave Quick Guide
Office of Biological Safety Autoclave Operation Quick Reference Guide Training: ALL users MUST undergo documented training for operation of the autoclave. Record each use of the autoclave in a log: Date, User ID, cycle type and nature of material in load Personal Protective Equipment (PPE) needed: ¾ Wear eye protection, lab coat, gloves along with heat resistant gloves. Rubberized apron, sleeve guards and face shield are recommended when autoclave is hot or splash risk is present. Hints and Precautions ¾ Become familiar with the manufacturer’s operations manual of your autoclave model(s). ¾ Plastics used for autoclaving MUST be labeled as autoclavable – otherwise the plastic will melt. ¾ Waste bags to be autoclaved must be loosely packed and not more than 2/3 filled. Steam must be able to penetrate to all contents of the bag. ¾ Sharps or pointed hard objects should not be placed directly into an autoclave bag; a thicker or rigid container must be used (such as a sharps container). ¾ Avoid overfilling an autoclave with loads or allowing a load to contact the chamber walls. ¾ Transferring waste contents from an overfilled bag to another bag should be avoided! This practice can lead to injury and/or exposure to contaminants. ¾ Do not leave an autoclave operating unattended for long periods of time; operation should be monitored periodically during a cycle in case of failure. ¾ Never autoclave solvents, combustible, volatile, flammable, radioactive or corrosive materials (e.g. ethanol, methanol, acids, bases, phenol) ¾ Remove extraneous items and combustible materials from around the autoclave exterior. Loading ¾ Follow manufacturer’s loading instructions for your autoclave model ¾ Transport loads on a cart and in secondary containers to reduce spills ¾ Clean item/container sterilization Loosen caps or lids to avoid dangerous pressure build-up during cycle Place containers in a tray and load the tray into the autoclave – this is easier to load and unload and will catch spills. -
Pouring Plates from Prepared Bottled Media
Pouring Plates from Prepared Bottled Media Primary Hazard Warning Never purchase living specimens without having a disposition strategy in place. When pouring bottles, agar is HOT! Burning can occur. Always handle hot agar bottles with heat-protective gloves. For added protection wear latex or nitrile gloves when working with bacteria, and always wash hands before and after with hot water and soap. Availability Agar is available for purchase year round. Information • Storage: Bottled agar can be stored at room temperature for about six months unless otherwise specified. Never put agar in the freezer. It will cause the agar to breakdown and become unusable. To prevent contamination keep all bottles and Petri dishes sealed until ready to use. • Pouring Plates • Materials Needed: • Draft-free enclosure or Laminar flow hood • 70% isopropyl alcohol • Petri dishes • Microwave or hot water bath or autoclave 1. Melt the agar using one of the following methods: a) Autoclave: Loosen the cap on the agar bottle and autoclave the bottle at 15 psi for five minutes. While wearing heat-protective gloves, carefully remove the hot bottle and let it cool to between 75–55°C before pouring. This takes approximately 15 minutes. b)Water Bath: Loosen the cap on the agar bottle and place it into a water bath. Water temperature should remain at around 100°C. Leave it in the water bath until the agar is completely melted. While wearing heat- protective gloves, carefully remove the hot bottle and let it cool to between 75–55°C before pouring. c) Microwave: Loosen the cap on the agar bottle before microwaving. -
Biohazardous Waste Handling for Eastern Kentucky University May 2018
Biohazardous Waste Handling For Eastern Kentucky University May 2018 Approved by The University Laboratory Safety Biohazard Subcommittee 1 Table of Contents Page Introduction 3-4 Definitions 5-6 Responsibilities and roles 7-9 Main body of document 10-17 Appendix 1 18-22 Autoclave procedures in SB 18-20 Autoclave procedures in Disney 218 21-22 Appendix 2 copy of IACUC form H: Use of hazardous agents 23 2 3 Introduction This document has been prepared to provide guidance to Eastern Kentucky University employees and students in the use and disposal of biohazardous materials in compliance with regulatory requirements. For this document “biohazardous waste” is defined as any discarded material which might include infectious laboratory materials or agents regulated by federal, state, and local authorities. At a minimum, the following categories should be considered as biohazardous waste materials: 1. Cultures and stocks of infectious biological agents, including laboratory waste, discarded live or attenuated viruses or related agents, culture dishes and other laboratory supplies used in the production or use of these agents, and any other related devices. 2. Human blood is a biohazardous waste. Human blood should treated in accordance with the “Eastern Kentucky University Bloodborne Pathogens Exposure Control Plan”. This plan can be found at the Risk Management Insurance/ Environmental Health and Safety website https://ehsrmi.eku.edu/occupational-safety. 3. Sharps: These are defined as needles, syringes, scalpels, etc., as well as any object sharp enough to puncture the skin (i.e. microscope slides, cover slips) that is used in the laboratories that could possibly come in contact with material that may be considered biohazardous waste. -
The Eppendorf Mechanical Pipettes Research® Plus and Reference 2 – Fully Autoclavable, Easy Adjustment, Quick and Simple Maintenance
APPLICATION NOTE No. 198 The Eppendorf Mechanical Pipettes Research® plus and Reference 2 – Fully Autoclavable, Easy Adjustment, Quick and Simple Maintenance Kornelia Ewald, Ulrike Gast, Eppendorf AG, Hamburg, Germany Abstract Research plus and Reference 2 pipettes are easy to clean safe to perform. This Application Note demonstrates the and maintain. Hence, routine maintenance can be easily special features of maintaining and cleaning Research performed by the user, saving valuable time. Readjust- plus pipettes and provides detailed information on ment of the pipette for liquids whose physical properties changing the pipette‘s adjustment. diff er signifi cantly from those of water is also easy and Introduction Research plus and Reference 2 are manual pipettes with Adjustment for specifi c liquids or altitude diff erent features and functional principles (e.g. one-button / During production, piston stroke pipettes are adjusted two-button operation). Fulfi lling the highest requirements, to distilled water under certifi ed measuring conditions. both pipettes have equal functionalities in terms of decon- To indicate the adjustment, all Research plus pipettes carry tamination, maintenance and adjustment. In order to meet an adjustment seal (Fig. 1). If necessary, adjustment for the high requirements of a modern laboratory, high quality specifi c liquids or for altitude can be carried out easily by piston stroke pipettes should be partly or fully autoclavable the user. The red adjustment seal, which is applied to the as well as UV resistant. adjustment opening following an adjustment, serves to The Eppendorf Research plus and Reference 2 pipettes can visualize a change of adjustment settings (Fig. 1). be decontaminated either by UV light or by autoclaving the entire instrument. -
Elara11 Autoclave Quick Installation Guide
OVER YEARS S ince 1925 Elara11 Autoclave Quick Installation Guide 1. Examine the outer carton and autoclave for any signs of damage. Immediately notify your dealer or Tuttnauer USA of any signs of damage. 2. To avoid injuries, lifting and carrying should be done by two people. • Lifting straps have been installed for your convenience. Lifting straps are for one time use only and should be removed and discarded after initial set up. 3. Place the sterilizer on a rigid level surface. The counter top or stand must be able to support 275lbs lbs Minimum 24”depth 4. The minimum depth of the counter top needs to be 24 inches. counter top required 5. It is mandatory to leave a minimum of 2” clearance between the back of the Elara11 and the wall. If located in a cabinet, the rear panel of the cabinet must be removed for proper air circulation. Failure to provide the needed clearance will result in failed cycles. 6. Side clearances should be a minimum of 2”. 7. Make sure all the feet are on the autoclave and none of them have been lost. 8. Connect the power cord to the socket on the rear of the autoclave; then plug it into the supply outlet. Power switch a. This unit requires a 230 volt 1 or 2 phase 15A supply. b. The acceptable operating voltage range is 220 to 235 volts. c. The installation of a Buck/Boost transformer (0.5KVA) may be required to meet the acceptable operating voltage. d. The supply outlet must be a properly grounded outlet. -
Laboratory Supplies and Equipment
Laboratory Supplies and Equipment Beakers: 9 - 12 • Beakers with Handles • Printed Square Ratio Beakers • Griffin Style Molded Beakers • Tapered PP, PMP & PTFE Beakers • Heatable PTFE Beakers Bottles: 17 - 32 • Plastic Laboratory Bottles • Rectangular & Square Bottles Heatable PTFE Beakers Page 12 • Tamper Evident Plastic Bottles • Concertina Collapsible Bottle • Plastic Dispensing Bottles NEW Straight-Side Containers • Plastic Wash Bottles PETE with White PP Closures • PTFE Bottle Pourers Page 39 Containers: 38 - 42 • Screw Cap Plastic Jars & Containers • Snap Cap Plastic Jars & Containers • Hinged Lid Plastic Containers • Dispensing Plastic Containers • Graduated Plastic Containers • Disposable Plastic Containers Cylinders: 45 - 48 • Clear Plastic Cylinder, PMP • Translucent Plastic Cylinder, PP • Short Form Plastic Cylinder, PP • Four Liter Plastic Cylinder, PP NEW Polycarbonate Graduated Bottles with PP Closures Page 21 • Certified Plastic Cylinder, PMP • Hydrometer Jar, PP • Conical Shape Plastic Cylinder, PP Disposal Boxes: 54 - 55 • Bio-bin Waste Disposal Containers • Glass Disposal Boxes • Burn-upTM Bins • Plastic Recycling Boxes • Non-Hazardous Disposal Boxes Printed Cylinders Page 47 Drying Racks: 55 - 56 • Kartell Plastic Drying Rack, High Impact PS • Dynalon Mega-Peg Plastic Drying Rack • Azlon Epoxy Coated Drying Rack • Plastic Draining Baskets • Custom Size Drying Racks Available Burn-upTM Bins Page 54 Dynalon® Labware Table of Contents and Introduction ® Dynalon Labware, a leading wholesaler of plastic lab supplies throughout -
Cleaning and Decontamination Guide for Sartorius Pipettes
Operating Manual Cleaning and Decontamination Guide for Sartorius Pipettes Version 1 / 2018 / 11 Contents Contents 1 Cleaning and Decontamination in Pipette Maintenance . 4 2 Cleaning Guide . 5 2 .1 Cleaning the outer surface of the pipette (daily) . 5 2 .2 Cleaning the lower part of the pipette (every three months) . 5 3 Application-Specific Cleaning and Decontamination of Pipettes . 10 3 .1 When cleaning Sartorius pipettes for specific applications . 10 3 .2 Cleaning and decontamination reagent quick-guide . 11 3 .3 Cleaning agents and their activities . 11 3 .4 Cleaning procedures . 12 3 .5 Decontamination agents and their activities . 12 3 .6 Decontamination procedures . 13 4 Autoclaving Guide . 14 4 .1 Mechanical pipettes . 14 4 .2 Electronic pipettes . 14 4 .3 Autoclaving quick-guide . 15 4 .4 Drying of pipettes . 15 5 Summary of Pipette Parts . 16 5 .1 Mechanical pipettes parts and materials . 16 5 .1 .1 Tacta® mechanical pipette . 16 5 .1 .2 mLine® mechanical pipette . 17 5 .1 .3 Proline® Plus mechanical pipette . 17 5 .1 .4 Proline® mechanical pipette . 18 5 .2 Electronic pipette parts and materials: Picus and Picus® NxT . 18 6 Contact . 19 6 .1 Further information about pipette cleaning, decontamination and maintenance . 19 6 .2 Pipette maintenance, servicing or calibration . 19 Cleaning and Decontamination Guide for Sartorius Pipettes 3 Cleaning and Decontamination in Pipette Maintenance 1 Cleaning and Decontamination in Pipette Maintenance Pipettes are precision instruments whose performance can be significantly impacted if not adequately maintained . To maintain the level of purity that is critical in many laboratory applications, adequate cleaning and decontamination of pipettes is necessary . -
The Effect of Autoclave Resterilisation on Polyester Vascular Grafts
CORE Metadata, citation and similar papers at core.ac.uk Provided by Elsevier - Publisher Connector Eur J Vasc Endovasc Surg 18, 386±390 (1999) Article No. ejvs.1999.0891 The Effect of Autoclave Resterilisation on Polyester Vascular Grafts G. Riepe∗1, M. S. Whiteley2, A. Wente1, A. Rogge1, A. SchroÈ der1, R. B. Galland2 and H. Imig1 1Department of General, Vascular and Thoracic Surgery, General Hospital of Hamburg±Harburg, Germany; 2Department of Surgery, Royal Berkshire Hospital, Reading, U.K. Objectives: polyester grafts are expensive, single-use items. Some manufacturers of uncoated, woven grafts include instructions for autoclave resterilisation to be performed at the surgeon's own request. Others warn against such manipulation. Theoretically, the glass transition point of polyester at 70±80°C and the possible acceleration of hydrolysis suggest that autoclave resterilisation at 135°C might be a problem. Materials and methods: a DeBakey Soft Woven Dacron Vascular Prosthesis (Bard) and a Woven Double Velour Dacron Graft (Meadox) were autoclave-resterilised 0 to 20 times, having been weighed before and after sterilisation. Tactile testing was performed. Mechanical properties were examined by probe puncture and single-®lament testing, the surface was examined by scanning electron microscopy and the degree of hydrolysis by infra-red spectroscopy. Results: tactile testing revealed a change of feeling with increasing cycles of resterilisation. Investigation of weight, textile strength, single-®lament strength, electron microscopy of the surface and infra-red spectroscopy showed no change of the material. Conclusions: changes felt are presumably a surface phenomenon, not measurably affecting strength or chemistry of material after autoclave resterilisation. -
WHEATON Media Bottles
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I. Direct Titration of Sulfate, II. High Precision Spectrophotometric Analysis Max Quentin Freeland Iowa State College
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1955 I. Direct titration of sulfate, II. High precision spectrophotometric analysis Max Quentin Freeland Iowa State College Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Analytical Chemistry Commons Recommended Citation Freeland, Max Quentin, "I. Direct titration of sulfate, II. High precision spectrophotometric analysis" (1955). Retrospective Theses and Dissertations. 14746. https://lib.dr.iastate.edu/rtd/14746 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMi films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand comer and continuing from left to right in equal sections with small overlaps. -
SPECIAL SCIENTIFIC REPORT-FISHERIES Na 349
349 CHEMICAL ANALYSES OF MARINE AND ESTUARINE WATERS USED BY THE GALVESTON BIOLOGICAL LABORATORY SPECIAL SCIENTIFIC REPORT-FISHERIES Na 349 UNITED STATES DEPARTMENT OF THE INTERIOR FISH AND WILDLIFE SERVICE United States Department of the Interior, Fred A. Seaton, Secretary Fish and Wildlife Service, Arnie J. Suomela, Commissioner Bureau of Commercial Fisheries, Donald L, McKernan, Director CHEMICAL ANALYSES OF MARINE AND ESTUARINE WATERS USED BY THE GALVESTON BIOLOGICAL LABORATORY by Kenneth T. Marvin, Zoula P. Zein-Eldin, Billie Z. May and Larence M. Lansford Chemists Galveston, Texas United States Fish and Wildlife Service Special Scientific Report— Fisheries No. 349 Washington, D. C. June 1960 CONTENTS Introduction 1 Sample treatment prior to analysis 1 Sample storage containers 2 Analytical methods 2 Standard samples 2 Phosphate 3 Inorganic only 3 Total and inorganic 3 Total only 4 Nitrate-nitrite 5 Nitrite 5 Salinity 6 Copper 6 Sulfide 7 Oxygen 7 Total carbon dioxide 8 Ammonia 10 Chlorophyll 10 "Carbohydrates" 11 "Protein" (tyrosine equivalent) 12 Washing procedure for all analytical glassware 12 Literature cited 13 111 CHEMICAL AMLYSES OF MAP.INE AND ESTOARIKE mTERS USED BY TBE GALVESTON BIOLOGICAL lABORATORY by Kenneth T. Marvin, Zoula P. Zein-Eldin, Billie Z. May and Larence M. Lansford ABSTRACT This paper describes the chemical techniques and procedures used hy the Biological lahoratory of the U. S. Bureau of Commercial Jlsherles, Galveston^ Texas, for analyzing samples Involved In the chemical and hlo- logical survey of the marine and estuarlne waters of the Gulf of Mexico and also In the many laboratory and field studies and experiments that have heen made pertaining to the red tide investigation.