Phase separation experiments in living cells

Phase separation experiments in living cells, Total:103 items.

The international standard classification for "Phase separation experiments in living cells" includes: Water of natural resources , Protection against dangerous goods , Pesticides and other agrochemicals , Internal combustion engines .

The Chinese standard classification for "Phase separation experiments in living cells" includes: Specifications for pollution control , Marking, packaging, transport and storage in general , Medical apparatus and devices in general , Engine body and moving parts , Pesticide management and application method .

Group Standards of the People's Republic of China

T/CSBM 0044-2023 Non-antibody-dependent magnetic separation detection method of circulating tumor cells in peripheral blood
T/SPEMF 0050-2023 Technical standards for selection of ligand-free on living cells
T/CMBA 011-2020 Collection, Separation and Preservation of PBMC from Human Peripheral Blood
T/YZXMR 001-2021 Isolation and culture method of dental pulp stem cells
T/CRHA 013-2022 Specification for menstrual blood-derived mesenchymal stem cells resource storage - Part 2：Isolation, processing and cryopreservation of menstrual blood-derived mesenchymal stem cells
T/SZLSBA 02-2023 Technical standards for selection of ligand-free on living cells
T/CSUS 31-2021 Water quality―Determination of the estrogenic potential of water and wastewater―In vitro human cell-based reporter gene assay
T/CRHA 007-2022 Specification for mononuclear cell resource storage in healthy blood donors Part 4：Isolation, processing and cryopreservation of mononuclear cells
T/SHRH 027-2019 In Vitro Test -Inhibition of Melanin Synthesis in B16 Cells Test

Professional Standard - Commodity Inspection

SN/T 2497.23-2010 Test method of import and export dangerous chemicals—Part 23:Separation of cellular organelles

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

GB/T 15670.17-2017 Toxicological test methods for pesticides registration. Part 17: Mammalian spermatogonial/spermatocyte chromosome aberration test
GB 2805-1981 Metallographic inspection for individually cast piston ring of reciprocating internal combustion engine
GB/T 21767-2008 Chemical - Test method of unscheduled DNA synthesis (UDS) test with mammalian liver cells In Vivo
GB/T 15670.16-2017 Toxicological test methods for pesticides registration. Part 16: In vivo mammalian bone marrow cell chromosome aberration test
GB/T 43279.1-2023 Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for venous whole blood—Part 1: Isolated cellular RNA
GB/T 43450-2023 Chemicals—In vitro cellular assay for acute eye irritation—TRPV1 activity detection method
GB/T 21773-2008 Chemicals - Test method of in vivo mammalian erythrocyte micronucleus

未注明发布机构

DIN ISO 13022 E:2013-07 Medical products containing viable human cells - Application of risk management and requirements for processing practices

国家食品药品监督管理局

YY/T 1465.4-2017 Immunogenic evaluation method of medical devices-Part4:Phagocytosis of mouse peritoneal macrophages on chicken erythrocytes- Ex-vivo method

Professional Standard - Machinery

JB/T 6016.1-2008 Internal combustion engines-Piston rings-Metallographic inspections-Part1:For singlecast cast iron
JB/T 6016-1992 Metallographic Examination of Single Cast Piston Ring of Internal Combustion Engine
JB/T 6290-1992 Metallographic Examination of Internal Combustion Engine Cylinder Casting Piston Ring
JB/T 6016.5-2011 Internal combustion engines — Piston rings — Metallographic inspections —Part 5：For boracic cast iron piston rings by individual cast
JB/T 6290-2007 Internal combustion engines-Sleeve cast piston rings-Metallographic inspections

Taiwan Provincial Standard of the People's Republic of China

CNS 14393.5-2004 Biological evaluation of medical devices – Part 5：Tests for in vitro cytotoxicity

American Society for Testing and Materials (ASTM)

ASTM E1398-91(2003) Standard Practice for the in vivo Rat Hepatocyte DNA Repair Assay
ASTM F2739-19 Standard Guide for Quantifying Cell Viability and Related Attributes within Biomaterial Scaffolds
ASTM F2739-16 Standard Guide for Quantifying Cell Viability within Biomaterial Scaffolds
ASTM E1398-91(2008) Standard Practice for In Vivo Rat Hepatocyte DNA Repair Assay
ASTM E1398-91(1998) Standard Practice for the in vivo Rat Hepatocyte DNA Repair Assay
ASTM F1903-18 Standard Practice for Testing for Cellular Responses to Particles in vitro
ASTM F2739-08 Standard Guide for Quantitating Cell Viability Within Biomaterial Scaffolds
ASTM F1906-98 Standard Practice for Evaluation of Immune Responses In Biocompatibility Testing Using ELISA Tests, Lymphocyte, Proliferation, and Cell Migration
ASTM E1397-91(2008) Standard Practice for In Vitro Rat Hepatocyte DNA Repair Assay
ASTM E1397-91(1998) Standard Practice for the in vitro Rat Hepatocyte DNA Repair Assay
ASTM E1397-91(2003) Standard Practice for the in vitro Rat Hepatocyte DNA Repair Assay
ASTM F3106-22 Standard Guide for in vitro Osteoblast Differentiation Assays
ASTM F34-13(2018) Standard Practice for Construction of Test Cell for Liquid Extraction of Flexible Barrier Materials
ASTM F1027-86(2012) Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices
ASTM F3088-14 Standard Test Method for Use of a Centrifugation Method to Quantify/Study Cell-Material Adhesive Interactions
ASTM E1263-97(2003) Standard Guide for Conduct of Micronucleus Assays in Mammalian Bone Marrow Erythrocytes
ASTM E1263-97 Standard Guide for Conduct of Micronucleus Assays in Mammalian Bone Marrow Erythrocytes
ASTM F2131-02 Standard Test Method for In Vitro Biological Activity of Recombinant Human Bone Morphogenetic Protein-2 (rhBMP-2) Using the W-20 Mouse Stromal Cell Line
ASTM F2131-02(2007)e1 Standard Test Method for In Vitro Biological Activity of Recombinant Human Bone Morphogenetic Protein-2 (rhBMP-2) Using the W-20 Mouse Stromal Cell Line
ASTM F2149-01(2007) Standard Test Method for Automated Analyses of Cells-the Electrical Sensing Zone Method of Enumerating and Sizing Single Cell Suspensions
ASTM F2149-01 Standard Test Method for Automated Analyses of Cells8212;the Electrical Sensing Zone Method of Enumerating and Sizing Single Cell Suspensions
ASTM F3106-14 Standard Guide for in vitro Osteoblast Differentiation Assays

KR-KS

KS M ISO 4590-2018 Rigid cellular plastics — Determination of the volume percentage of open cells and of closed cells
KS P ISO 13022-2018(2023) Medical products containing viable human cells — Application of risk management and requirements for processing practices

HU-MSZT

MSZ KGST 2702-1980 Laboratory diagnosis of yak leukocyte disease

Korean Agency for Technology and Standards (KATS)

KS M ISO 4590:2018 Rigid cellular plastics — Determination of the volume percentage of open cells and of closed cells
KS P ISO 13022-2023 Medical products containing viable human cells — Application of risk management and requirements for processing practices

SCC

AWWA JAW30405 Journal AWWA — Inactivation of Cell-Associated and Dispersed Hepatitis A Virus in Water
AAMI/ISO 13022:2012 Medical products containing viable human cells -- Application of risk management and requirements for processing practices
DANSK DS/ISO 13022:2012 Medical products containing viable human cells - Application of risk management and requirements for processing practices
BS PD CEN/TS 17688-1:2021 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for Fine Needle Aspirates (FNAs)-Isolated cellular RNA
CSA ISO 20186-1:2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
10/30203224 DC BS ISO 13022. Medical products containing viable human cells. Application of risk management and requirements for processing practices
SN-CEN/TS 17688-1:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA
DIN CEN/TS 17688-1:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA; German version CEN/TS 17688-1:2021
DIN ISO 13022 E:2013 Draft Document - Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
DIN EN ISO 20186-3 E:2018 Draft Document - Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Cellular RNA - Part 3: Isolated circulating cell free DNA from plasma (ISO/DIS 20186-3:2018); German and English version...
DANSK DS/CEN/TS 17688-1:2022 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) – Part 1: Isolated cellular RNA
CAN/CSA-ISO 20186-3-2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma
BS PD CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood-Isolated cellular RNA
DANSK DS/CEN/TS 17811:2022 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for urine and other body fluids – Isolated cell free DNA
SN-CEN/TS 17811:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA
BS PD CEN/TS 17811:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for urine and other body fluids. Isolated cell free DNA
BS PD CEN/TS 17742:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood. Isolated circulating cell free RNA from plasma
DIN CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma; German version CEN/TS 17742:2022
AWWA PATH56522 Applications of In-Vitro Cell Culture for Measuring Infectivity and Inactivation of Cryptosporidium parvum
DANSK DS/CEN/TS 17742:2022 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for venous whole blood – Isolated circulating cell free RNA from plasma

US-AAMI

ANSI/AAMI/ISO 13022:2012 Medical products containing viable human cells.Application of risk management and requirements for processing practices

API - American Petroleum Institute

API PUBL 32-32288-1985 ACTIVITY OF API81-04 IN THE ACUTE IN VIVO CYTOGENETICS ASSAY IN MALE AND FEMALE RATS
API PUBL 33-30493-1985 ACTIVITY OF API 83-08 IN THE ACUTE IN VIVO CYTOGENETICS ASSAY IN MALE AND FEMALE RATS

International Organization for Standardization (ISO)

ISO 13022:2012 Medical products containing viable human cells - Application of risk management and requirements for processing practices
ISO 20186-3:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma

British Standards Institution (BSI)

PD CEN/TS 17688-1:2021 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for Fine Needle Aspirates (FNAs). Isolated cellular RNA
PD CEN/TS 17811:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for urine and other body fluids. Isolated cell free DNA
BS EN ISO 10993-5:1999 Biological evaluation of medical devices - Tests for in vitro cytotoxicity
BS EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated cellular RNA

German Institute for Standardization

DIN ISO 13022:2014-06 Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
DIN 58933-1:1995-01 Haematology - Procedure for determining the volume fraction of erythrocytes (packed cell volume) in blood - Part 1: Reference method based on centrifugation
DIN ISO 13022:2014 Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
DIN CEN/TS 17688-1:2022-06 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA; German version CEN/TS 17688-1:2021
DIN CEN/TS 17811:2022-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA; German version CEN/TS 17811:2022

GSO

GSO ISO 13022:2016 Medical products containing viable human cells -- Application of risk management and requirements for processing practices
OS GSO ISO 13022:2016 Medical products containing viable human cells -- Application of risk management and requirements for processing practices
GSO ISO 20186-1:2024 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA

RU-GOST R

GOST R ISO 13022-2016 Medical products containing viable human cells. Application of risk management and requirements for processing practices

European Committee for Standardization (CEN)

EN ISO 20186-3:2019 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)
FprCEN/TS 17688-1-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA
CEN/TS 17688-1:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA
CEN/TS 17811:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA
prEN ISO 18704 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA
EN ISO 10993-5:2009 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)

ES-UNE

UNE-CEN/TS 17688-1:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA (Endorsed by Asociación Española de Normalización in February of 2022.)

AT-ON

ONR CEN/TS 17688-1-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA

Association Francaise de Normalisation

NF EN ISO 29701:2011 Nanotechnologies - Endotoxin detection test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test
NF S92-075-1*NF EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1 : isolated cellular RNA
NF V04-040-1:1997 Milk. Enumeration of somatic cells. Part 1 : microscopic method.
NF EN ISO 17099:2018 Radioprotection - Performance criteria for laboratories carrying out biological dosimetry using the micronucleus test with blockade of cytodieresis (CBMN) in peripheral blood lymphocytes

AENOR

UNE 103405:1994 GEOTECHNICS. ONE-DIMENSIONAL CONSOLIDATION TEST IN AN EDOMETRIC CELL.

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