SDSWholeCellExtracts

-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 125 ml flask.***Since it is often difficult to estimate the growth rate of yeast, it is helpful to start several 25 ml cultures, each with a different dilution of the starter culture (e.g. 1:100, 1:300, 1:900).2. Grow at 30 C shaking (250 rpm) until the OD600 nm ~ 1.0 (Th......阅读全文

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

酵母准备

Yeast DNA PreparationYeast Genomic Preparation  (Gottschling Lab)Rapid method for yeast genomic DNA isolation  Yeast DNA Preparation (rapid glass bead

Small-Scale-Yeast-Whole-Cell-Extract-for-IP

Grow 100 ml yeast cells in desired media overnight to an A600 of ~1.0 (0.6 to 1.2 works well). For growth in minimal media, 1 ml of a saturated overni

Western-blotting样品准备-(一)

实验概要Preparation of  lysis buffers, protease and phosphatase inhibitors, lysate from cell  culture, lysate from tissues, protein concentration, samples

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

Western-blotting样品准备

实验概要Preparation of  lysis buffers, protease and phosphatase inhibitors, lysate from cell  culture, lysate from tissues, protein concentration, samples

MT-Spindowns-from-Extracts

MT Spindowns from ExtractsArshad DesaiNotes:The key variable in MT spindown experiments is ATP. Under high ATP conditions,conventional MAPs are select

Sample-preparation-(analytical-gels)

Sample preparation and solubilization are crucial factors for the overall performance of the 2-D PAGE technique. Protein complexes and aggregates shou

无创血压计应用论文:动物用血压计(二)

Measurements of Blood Pressure and Heart Rate-Systolic blood pressure and heart rate were measured using a noninvasive computerized tail-cuff syst

Cell-Extraction-Protocol

实验概要Primary tissues  are valuable tools for the study of intracellular and extracellular  markers which characterize disease states. We have developed

Whole-mount-fluores...

实验概要The method  provides a protocol for whole mount fluorescent immunohistochemistry.  The advantage of using fluorescence to stain whole mount sectio

IMMUNOHISTOCHEMISTRY-ON-WHOLE-MOUNT-EMBR

Dechorionate directly on apple juice/agar plates with 50-60 chlorox; embryos will float to the surface after 2-3''.Collect embryos on a Millip

Zebrafish-whole-mou...

实验概要Whole mount staining of Zebrafish embryos, now commonly used, requires extra steps to fix and permeabilize to ensure the egg membrane is perme

Immunofluorescence-Whole-Mount

Objective:Immunohistochemistry allows visualization of antigens (usually proteins) within an embryo. Typically, a primary antibody binds specifically

Methods-for-the-Measurement-of-a-Bacterial-Enzyme-Activity-in-Cell-Lysates4

The use of a micro-titre based colorimetric assay provided a third method for the study of ACTase activity, and the most useful for large scale measur

Cellfree-System-for-the-examination-of-apoptotic-activity

 IntroductionIn our lab we use the term 'cell-free system' when we talk about the examination of apoptotic activity in cytoplasmic extracts. T

Methods-for-the-Measurement-of-a-Bacterial-Enzyme-Activity-in-Cell-Lysates

AbstractThe kinetic characteristics and regulation of aspartate carbamoyltransferase activity were studied in lysates and cell extracts of Helicobacte

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

Preparation-of-cytoplasmic-extracts-for-the-application-inacellfree-system

Characteristics of this procedure:Cells are grown to 80% confluency, then harvested, washed and disrupted in KPM buffer by freezing-thawing cycles wit

Whole-mount-TUNEL-analysis-of-Xenopus-embryos

Fixation and pretreatmentDejelly albino embryos carefully in 2% Cystein (pH 7.8).Remove the vitellin membrane with two pairs of tweezers         (or c

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

美国实验室wetern方法

WESTERN BLOT PROTOCOLIn a Western blot, proteins that are separated on polyacrylamide gels on the basis of size are transferred to a membrane for dete

Nuclear-Extraction-Protocol

实验概要The procedure presented below describes a method for extracting nuclear from several cell lines of human origin.主要试剂Hypotonic Buffer Solution20 mM

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

96Well-Sample-Preparation-for-Adherent-Cells

实验概要The procedure  presented below describes a facile method for studying signal  transduction events with adherent cells (HeLa, MCF-7, BALB/c 3T3, et

96Well-Sample-Preparation-for-Adherent-Cells

实验概要The procedure  presented below describes a facile method for studying signal  transduction events with adherent cells (HeLa, MCF-7, BALB/c 3T3, et

96Well-Sample-Preparation-for-Suspension-Cells

实验概要The procedure  presented below describes a facile method for studying signal  transduction events with suspension cells (Jurkat, Raji, THP-1, etc.

96Well-Sample-Preparation-for-Suspension-Cells

实验概要The procedure  presented below describes a facile method for studying signal  transduction events with suspension cells (Jurkat, Raji, THP-1, etc.

96Well-Sample-Preparation-for-Suspension-Cells

实验概要The  procedure presented below describes a facile method for studying signal  transduction events with suspension cells (Jurkat, Raji, THP-1, etc.