№ lp_1_2_49570
File format: docx
Character count: 4063
File size: 857 KB
Year:
2014
Region / city:
Bethesda, MD
Topic:
Hematology, Immunohematology, Laboratory Procedures
Document Type:
Procedure Manual
Organization / Institution:
American Association of Blood Banks
Author:
Roback JD
Target Audience:
Laboratory personnel, medical professionals
Period of validity:
Ongoing, as of revision date
Approval Date:
March 1, 2014
Date of Changes:
March 1, 2014
References:
AABB Technical Manual, 17th ed., Methods in Immunhematology 3rd ed., Standards for Hospital Transfusion Services Version 3
Scope:
The document provides instructions for the removal of antibodies from coated red blood cells using freeze-thaw elution techniques, specifically for investigating ABO hemolytic disease of the fetus and newborn.
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
The product description is provided for reference. Actual content and formatting may differ slightly.
Section Number:
33 47 16
Title:
Temporary Exposed Geomembrane Cover Using Woven Coated Polyethylene
Product Name:
RhinoSkin™ Woven Coated Polyethylene Geomembrane
Material Type:
Woven Coated Polyethylene (WCPE)
Available Thicknesses:
12 mil, 16 mil, 20 mil, 24 mil
Standards Referenced:
ASTM D751; ASTM D4218; ASTM D4355; ASTM D4833; ASTM D5261; ASTM E96; ASTM G154
Manufacturer:
Owens Corning
Manufacturer Address:
One Owens Corning Parkway, Toledo, OH 43659
Application:
Temporary Exposed Geomembrane Cover (TEGC)
Warranty Period:
1.5, 2, 2.5, or 10 years (exposed applications)
Quality Requirements:
Manufacturer Quality Control Program and Certificate of Compliance required
Minimum Manufacturer Experience:
5 years continuous production; 5,000,000 square feet produced in last 5 years
Minimum Fabricator Experience:
5 years continuous fabrication; 5,000,000 square feet fabricated in last 5 years
Minimum Installer Experience:
5 years continuous installation; 5,000,000 square feet installed in last 5 years
Labeling Requirements:
Manufacturer name, fabricator name (if applicable), product identification, production date, thickness, roll dimensions, roll or panel number, deployment instructions
Storage Requirements:
Protected from damage; sacrificial cover required if stored on site more than six months; maximum stacking three rolls high
Testing Requirements:
Physical and mechanical properties verified by ASTM test methods
Intended Use:
Exposed geomembrane liner applications
Year:
2024
Region / City:
Global
Topic:
Antimicrobial Activity, Silver Nanoparticles, Green Synthesis
Document Type:
Research Article
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Researchers, Scientists in Biotechnology, Microbiology, and Nanotechnology
Period of Validity:
Not applicable
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2026
Region / City:
Not specified
Subject:
Building insulation materials
Document Type:
Technical specification
Organization / Institution:
Atlas Roofing Corporation
Author:
Not specified
Target Audience:
Specification writers and construction professionals
Applicable Period:
Project-specific
Approval Date:
Not specified
Revision Date:
Not specified
Material Standards:
CAN/ULC S704-03, ASTM D 1621, ASTM D 1623, ASTM C 203, ASTM D 2842, ASTM D 2126, ASTM E 96
Fire Performance:
Flame spread less than 500, Smoke developed <500
Board Sizes:
1219 mm x 2438 mm, 1219 mm x 2743 mm, 406 mm x 2438 mm, 610 mm x 2438 mm
Thickness Options:
13 mm, 19 mm, 25 mm, 38 mm, 51 mm, 64 mm, 76 mm, 89 mm, 102 mm
Thermal Performance:
RSI values from 0.53 to 4.40, R-values from 3.0 to 25
Compressive Strength:
>140 kPa
Tensile Strength:
>35 kPa
Flexural Strength:
>275 kPa
Water Vapour Permeance:
>60 ng/(Pa s m2)
Water Absorption:
<3.5% by volume
Dimensional Stability:
<1% linear change
Service Temperature Range:
-73ºC to +122ºC
Sustainability:
Produced without HCFC, CFC, HFC blowing agents
Submittals:
Product test reports, data sheets, samples, LEED documentation if applicable
Waste Management:
Separate and recycle materials per project requirements
Year:
N/A
Region / City:
N/A
Topic:
Quality Control, Blood Grouping, Antibody Screening
Document Type:
Standard Operating Procedure
Organization / Institution:
N/A
Author:
N/A
Target Audience:
Laboratory personnel involved in blood grouping and antibody screening
Period of validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2018
Disorder Type:
Neuro-inflammatory disease
Target:
Central nervous system
Symptoms:
Optic neuritis, spinal cord inflammation, demyelination
Diagnosis:
Positive MOG antibody test, MRI evidence of demyelination
Treatment:
Immunoglobulin therapy (IVIG/SCIG), other therapies as determined by physician
Prevalence:
1 per 500,000 people
References:
Fan S et al., 2018; Kezuka T & Ishikawa H, 2018; Dos Passos GR et al., 2018; Weber MS et al., 2018
Journal:
World Journal of Gastrointestinal Pathophysiology
Manuscript Type:
Original Article
Study Design:
Retrospective Cohort Study
Authors:
Hyun Ah Chung; Sun-Young Lee; Hee Won Moon; Jeong Hwan Kim; In-Kyung Sung; Hyung Seok Park; Chan Sup Shim; Hye Seung Han
Affiliations:
Department of Internal Medicine, Department of Laboratory Medicine, and Department of Pathology, Konkuk University School of Medicine, Seoul 05030, South Korea
Corresponding Author:
Sun-Young Lee, MD, PhD
Country:
South Korea
Funding:
Supported by Konkuk University in 2015 (No. KU2015-A019-0270)
Institutional Review Board Approval:
Konkuk University School of Medicine (KUH1010625)
Clinical Trial Registration:
ClinicalTrials.gov ID: KCT0001302
Received:
December 27, 2015
Accepted:
July 11, 2016
Publication Year:
2016
Keywords:
Antibody; Helicobacter pylori; Hepatitis B; Immunoglobulin G; Pepsinogen
License:
Creative Commons Attribution Non Commercial (CC BY-NC 4.0)
Year:
2023
Region / City:
Not specified
Topic:
Anti-nuclear antibody testing, technical issues
Document type:
Update
Author:
Dr. Anna McHugh
Target audience:
Healthcare professionals
Action period:
May 2023
Approval date:
Not specified
Change date:
16th May 2023
Context:
The document is an update on delays and technical issues with anti-nuclear antibody testing, outlining the steps being taken to resolve the situation and advising healthcare professionals on necessary actions for patients.
Year:
2024
Region / city:
Hull, United Kingdom
Topic:
Coeliac Disease Screening
Document Type:
Medical Guidelines
Organization:
NHS
Author:
Anna McHugh
Target Audience:
Healthcare Professionals
Period of Validity:
From January 2023
Approval Date:
Not specified
Date of Changes:
February 2024
Year:
2023
Region / City:
Not specified
Topic:
Monoclonal antibody sequences, growth rate inhibition in cell models
Document type:
Research Supplementary Material
Organization / Institution:
Not specified
Author:
Not specified
Target audience:
Researchers, biomedical professionals
Effective period:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Year:
2012
Region / City:
United Kingdom
Subject:
Blood Grouping, Red Cell Antibody Testing, Pregnancy
Document Type:
Audit Tool
Institution:
British Committee for Standards in Haematology (BCSH)
Author:
N/A
Target Audience:
Healthcare professionals involved in blood transfusion, obstetrics, and fetal medicine
Period of Application:
Ongoing
Date of Approval:
N/A
Date of Changes:
N/A
Year:
2021
Region / city:
Various locations in the United States
Topic:
COVID-19 Treatment
Document type:
Clinical Trial Report
Institution:
Regeneron Pharmaceuticals, NIAID/CoVPN
Author:
Multiple investigators and research teams
Target audience:
Healthcare professionals, researchers, clinical trial coordinators
Period of validity:
Study conducted during 2020-2021
Approval date:
Not specified
Date of changes:
Not specified
Year:
2026
Region / City:
Canada, multiple cities
Subject:
COVID-19 treatment eligibility
Document Type:
Medical referral form
Organization / Institution:
Health Canada; regional hospitals
Author:
Clinicians completing referral
Target Audience:
Healthcare providers and eligible patients
Eligibility Criteria:
Adults and pediatric patients ≥12 years, ≥40 kg, at high risk of severe COVID-19
Treatment Window:
Within 7 days of symptom onset
Authorization:
Interim authorization (Interim Order) by Health Canada
Patient Data Fields:
Name, Date of birth, Allergies, Address, Contact information, Health Card Number
Clinical Criteria:
Symptomatic status, vaccination status, comorbidities, immunosuppression, prior COVID-19 infection
Referral Confirmation:
Clinician attestation with signature, date, and College number
Year:
2023
Region / city:
Rockville, MD, United States; Ottawa, ON, Canada
Topic:
NMR assignments, antibody research, protein expression
Document type:
Research article
Institution:
Institute for Bioscience and Biotechnology Research, National Institute of Standards and Technology, University of Maryland; Centre for Oncology, Radiopharmaceuticals and Research, Biologics and Radiotherapeutic Drugs Directorate, Health Canada
Author:
Tsega L. Solomon, Kinlin Chao, Genevieve Gingras, Yves Aubin, William B. O’Dell, John P. Marino, Robert G. Brinson
Target audience:
Researchers in biochemistry, protein chemistry, pharmaceutical sciences
Effective period:
2023 and onwards
Approval date:
N/A
Date of changes:
N/A
Keywords:
backbone assignments, Fab domain, NISTmAb, biologics, monoclonal antibodies
Context description:
This document presents the results of a study on the backbone NMR assignments of the yeast-expressed Fab fragment of the NISTmAb antibody, aimed at advancing structural characterization techniques for monoclonal antibodies.
Instrument:
Immucor Galileo Echo
Test Panels:
Capture-R Ready-ID; Capture-R Extend I; Capture-R Extend II
Test Method:
IgG antibody panel using Capture-R technology
Temperature:
37°C
Specimen Type:
EDTA anticoagulated whole blood; serum from fully clotted blood
Specimen Stability:
≤5 days from collection; ≤4 days for recently transfused or pregnant patients
Exclusion Criteria:
Hemolyzed (≥3+), lipemic, or icteric samples not accepted
Reagents:
Capture LISS; Capture-R Ready-ID; Capture-R Extend I & Extend II; Capture-R Indicator Cells; WB corQC; PHIX buffered saline
Equipment:
Immucor Galileo Echo
Quality Control:
Commercial WB corQC performed daily; 24-hour control interval after validation
Controls:
Positive and negative controls included in each 14-cell panel
Related Policy:
SWIM manual NRT.007 “Antibody Identification of Warm Reactive Antibodies”
Reporting:
Results reviewed and confirmed by technologist; specimens forwarded for additional antibody testing if required
Restrictions:
Partially used strips cannot be reused
References:
Galileo Echo Operator Manual; SWIM manual
Year:
2022
Region / City:
Belfast
Subject:
COVID-19, SARS-CoV-2, antibody neutralisation
Document type:
Research study call
Organization / Institution:
Queen’s University Belfast
Author:
Ultan Power
Target audience:
Healthy volunteers aged 18-65
Study period:
Ongoing
Approval date:
Not specified
Modification date:
Not specified
Year:
2023
Region / city:
Not specified
Topic:
Recombinant proteins, antibodies, and reagents for macrophage polarization and related techniques
Document type:
Laboratory protocol
Institution:
Not specified
Author:
Not specified
Target audience:
Researchers in molecular biology and immunology
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Year:
N/A
Region / city:
N/A
Topic:
irMG clinical manifestations and treatment outcomes
Document Type:
Clinical data table
Institution / Organization:
N/A
Author:
N/A
Target Audience:
Medical professionals, researchers
Period of validity:
N/A
Approval date:
N/A
Date of changes:
N/A
Note:
Contextual description
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.