Method:PreparationofLymphocyteCellPelletforStorage

Method: Preparation of Lymphocyte Cell Pellet for StorageJune 10, 1990Rosalie VeilePurpose:Following propagation to 1 X 108 cells, lymphoblastoid cells are conveniently stored at -80 degrees C to preserve the high molecular weight DNA in the cells until the DNA is purified. This procedure describes the steps required to harvest and freeze the cells for long term storage.Time required:2-3 hours to prepare 12-15 cultur......阅读全文

Method:-Preparation-of-Lymphocyte-Cell-Pellet-for-Storage

Method: Preparation of Lymphocyte Cell Pellet for StorageJune 10, 1990Rosalie VeilePurpose:Following propagation to 1 X 108 cells, lymphoblastoid cell

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

Method:-Lymphocyte-Transformation

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

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

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

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

Easy-YAC-Preparation-Method

YAC TRANSFORMATION OF C. ELEGANS USING TOTAL YEAST GENOMIC DNA[This method is described in The Worm Breeder's Gazette (1997) A. Davies and J. Shaw

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 ·  

Column-Method-for-Lambda-Phage-DNA-Preparation

Purpose:Mini-prep method for lambda phage DNA purification from lysates.Time required:4 hours once the lysate is in handSpecial supplies required:BioR

DNA转化

DNA转化Chemical Transformation·         Transformation of Competent Cells (RbCl2 Method) (Goldberg Lab)Very nice protocol for E. Coli transformation inc

B-Lymphocyte-Cell-Surface-Molecules

B cells must communicate with their environment to participate in the immune system as the source of antigen-specific immunoglobulins. Cell surface pr

CellTrace™-CFSE-Cell-Proliferation-Kit

实验概要The CellTrace™  CFSE Cell Proliferation Kit provides a versatile and well-retained  cell-tracing reagent in a convenient and easy-to-use form. The

Culture-of-Peripheral-Blood-Lymphocytes-for-Chromosome-Analysis

实验概要Provide information about chromosomal abnormalities.实验原理The  blood cell karyotyping method was developed to provide information  about chromosomal

Optimized-Method-for-the-Preparation-of-Rodent-Testicular-Cells3

Moreover, when the method was applied to the analysis of the cellular composition of immature testes, the results were also in agreement with previous

Optimized-Method-for-the-Preparation-of-Rodent-Testicular-Cells1

Homogeneity of cell populations is a prerequisite for the analysis of biochemical and molecular events during male gamete differentiation. Given the c

A-practical-method-for-the-preparation-of-total-DNA-from-filamentous-fungi

Most methods of DNA preparation from fungi are time-consuming due to the need to first make protoplasts, expensive for chemicals such as cesium chlori

Optimized-Method-for-the-Preparation-of-Rodent-Testicular-Cells2

Flow Cytometric AnalysisPrior to flow cytometric analysis, the vital dye Hoechst 33342 (Sigma-Aldrich, St. Louis, MO, USA) was added to cell suspensio

CELL-MEMBRANE-PREPARATION

I.  Solutions: A.  Ca and Mg free Phosphate Buffered Saline (PBS) solution,   buffered with 0.02M Hepes.  pH=7.4 B.  Ca and Mg free PBS, buffered with

Competent-Cell-Preparation

实验概要Competent cells are those that possess more easily altered cell walls that DNA can be passed through easily. These cells readily incorporate f

RNA提取

RNA提取(主要内容如下)Tips for Handing RNA Total RNA IsolationmRNA IsolationrRNA IsolationOthersQ & A posted in the Method Forum  Basic Procedures for Handing

Method:-Cell-Counts-Using-a-Hemacytometer

Method: Cell Counts Using a HemacytometerJune 1, 1990Rosalie VeilePurpose:The purpose of this procedure is to determine the cell density of the cultur

Method:-Maintaining-Lymphoblastoid-Cell-Lines

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

体外荧光法检测核内体早期动力学5

Leave tubes on ice and repeat Steps 13–15 for the next 6–12 plates of cells.When all cells are collected, centrifuge all tubes at 250g for 5 min at 4

DNA转化实验指导1

CONTENT Transformation-Competent E. coli preparation   Inoue "ultra-competent" methodRubidium chloride methodCosmid packaging protocol DNA Ligation an

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

Preparation-of-Rat-Liver-Cell-Cytosol

These protocols should yield enough cytosol and organelles for 1-200 MT/Organelle motility assays.Solutions and Reagents  Freshly removed or flash fro

Cosmid-Cloning:-Cell-preparation,-DNA-packaging,-and-Cell-Transfection

Cosmid Cloning: Cell preparation, DNA packaging, and Cell TransfectionProtocol taken from Stratagene's Gigapack packaging extracts instruction man

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

Immunoprecipitation

Immunoprecipitation (IP) is one of the most widely used immunochemical techniques. Immunoprecipitation followed by SDS-PAGE and immunoblotting, is rou