Method:LymphoblastoidCellLinesfromFrozenWholeBlood

Method: Lymphoblastoid Cell Lines from Frozen Whole BloodMay 31, 1990Rosalie VeilePurpose:Blood Samples can be stored frozen as a backup in case an LCL is needed at a later date.Time required:15 minutes to freeze 1-4 cryotubes placing them directly into the -135 degrees C freezer; orone hour to freeze the tubes using the Cryomed freezing chamber. Cells have been shown to be more viable if temperature is lowered gradu......阅读全文

Method:-Lymphoblastoid-Cell-Lines-from-Frozen-Whole-Blood

Method: Lymphoblastoid Cell Lines from Frozen Whole BloodMay 31, 1990Rosalie VeilePurpose:Blood Samples can be stored frozen as a backup in case an LC

Method:-Maintaining-Lymphoblastoid-Cell-Lines

Method: Maintaining Lymphoblastoid Cell LinesJune 10, 1990Rosalie VeilePurpose:To grow lymphoblastoid cells for permanent storage and for DNA extracti

巨噬细胞和单核白细胞

·         Lymphocyte Transformation (Donis-Keller lab)Lymphocytes are transformed to establish cell lines. Mononuclear cells (lymphocytes) from antico

Method:-Preparation-of-Lymphoblastoid-Cell-Lines-for-Long-Term-Storage

Method: Preparation of Lymphoblastoid Cell Lines for Long Term StorageMay 30, 1990Rosalie VeilePurpose:To store cell lines in a form that will insure

细胞培养常规操作

常规操作(主要内容如下)·         Aseptic Technique·         Culture Vessels·         Cell Counting·         Primary Culture·         Maintenance of Cell Line ·  

Resuscitation-of-Frozen-Cell-Lines

AimMany cultures obtained from a culture collection, such as ECACC, will arrive frozen and in order to use them the cells must be thawed and put into

Serum-Separation-from-Whole-Blood

Serum Separation from Whole Blood1) Collect sample (preferably in glass tubes) and leave for 1 hour at 37°C to allow it to clot.2) Leave sample at 4°C

Separation-of-Platelets-from-Whole-Blood

PurposeThis protocol describes how to isolate human platelets from whole blood. Isolated platelets are used for static adhesion assays, for flow chamb

Method:-Logging-in-Specimens-and-Record-Keeping

Method: Logging in Specimens and Record KeepingJune 10, 1990Rosalie VeilePurpose:To keep a written and computerized record of all cell lines, the date

Direct-PCR-from-Whole-Yeast-Cells:-Zymolyase-Method

Direct PCR from Whole Yeast Cells: Zymolyase MethodContributor: Namjin ChungDate: June 18, 19961. An average-size yeast colony (0.5-2mm) or a cell pel

Method:-Reactivating-Cell-Lines-and-Cell-Growth-for-DNA-Preparation

Purpose:Cell lines are reactivated and grown to a count of 1 x 108 cells. The cells are pelleted and stored frozen at -80 degrees C prior to DNA extra

SQ-Blood-DNA-Midi-Protocol-for-500l3ml-whole-blood

实验概要The E.Z.N.A.®  SQ Blood DNA Kit is designed for isolating high molecular weight  genomic DNA from fresh, frozen or anticoagulated whole blood. The

SQ-Blood-DNA-Maxi-Protocol-for-410-ml-whole-blood

实验概要The E.Z.N.A.®  SQ Blood DNA Kit is designed for isolating high molecular weight  genomic DNA from fresh, frozen or anticoagulated whole blood. The

细胞培养——细胞保藏

Working Cell Bank (Contributed by Nanci Donacki)Provides detailed protocol for establishing a working cell bank    Master Cell Bank (Contributed by Na

Extraction-of-RNA-from-Frozen-Sections

RNA Extraction from Frozen Tissue Sections Tissue Handling: Note that all unfixed human tissue should be handled as BioSafety Level 2 materials (wear

DNA抽提

DNA抽提(主要内容如下)·   Working with DNA·   DNA Extraction from Bacteria and Other Organisms·   DNA Extraction from Cell and Tissue·   Mitochondria DNA Isola

Subculture-of-Suspension-Cell-Lines

AimIn general terms cultures derived from blood (e.g. lymphocytes) grow in suspension. Cells may grow as single cells or in clumps (e.g. EBV transform

DNA-Extraction-from-Blood

实验概要The ChargeSwitch®  gDNA Purification Kits allow rapid and efficient purification of  genomic DNA from small volumes of human blood. After preparin

酵母转化

·         Yeast Transformation (Gietz Lab)LiAc/SS-DNA/PEG Transformation·         Yeast Transformation (Breeden Lab)LiAc method·         Large-Scale Y

DNA-Extraction-from-Frozen-Tissue-Sections

Tissue collection, storage, microdissection, sectioning: See separate protocol.Tissue handling: Note that all fresh tissue should be handled as BioSaf

Protein-extraction-from-whole-tissues-for-IEF

Modified from that of Jay Thelen - University of Missouri-ColumbiaPhenol extraction followed by methanolic ammonium acetate precipitation - an effecti

SQ-Blood-DNA-Mini-Protocol-for-Buffy-Coat

实验概要The buffy coat fraction of whole blood is enriched with WBC, and usually gives at least 5-fold more DNA than the same volume of blood. To prep

Cryopreservation-of-Cell-Lines

AimThe protocol below describes the use of passive methods involving an electric -80ºC freezer for the cryopreservation of cell cultures. ECACC routin

Method:-Lymphocyte-Transformation

Method: Lymphocyte TransformationMay 30, 1990Rosalie VeilePrinciple:Lymphocytes are transformed to establish cell lines. Mononuclear cells (lymphocyte

Standard-Protocol-For-Up-to-10-ml-Whole-Blood

实验概要The E.Z.N.A.®  Blood DNA Maxi Kit is designed for isolation of genomic DNA from up to  25 ml of fresh, whole blood treated with any common anticoa

Harvesting-lymphocytes-from-Peripheral-Blood

Blood Harvest·        Anesthetize mice with 50ml of Xylene-Ketamine(2:1) coctail·        Pin animal to a board (use distal extremities) supine·       

Protocol-for-Isolating-DNA-from-Blood-with-Nucleated-Red-blood-Cells

实验概要DNA  isolation from fish or avian blood sample can be difficult because it  contains nucleated red blood cells. E.Z.N.A. NRBC Blood DNA Kit is  de

Red-Blood-Cell-Lysis-Protocols

实验概要BioLegend’s  Red Blood Cell (RBC) Lysis Buffer (Cat. No. 420301) has been designed,  formulated, and tested to ensure optimal lysis of RBCs in sin

Subculture-of-Adherent-Cell-Lines

AimAdherent cell lines will grow in vitro until they have covered the surface area available or the medium is depleted of nutrients. At this point the

SDS-Whole-Cell-Extracts

-Use sterile technique and sterile solutions in steps 1 to 3.-1. Using a saturated starter culture, inoculate 25 to 30 ml of appropriate media in a 12