PreparationofMitochondriafromRatLiver

Preparation of Mitochondria from Rat LiverRat liver is an ideal source for functional intact mitochondria for a number of reasons. We use Sprague-Dawley albino male rats for our studies. Female rats can be used, however for serious studies we usually stick to males to avoid complications due to the estrous cycle. Animal tissue is preferable to plant tissue because they do not have cell walls, which make homogenizatio......阅读全文

线粒体的结构与功能

In an attempt to be concise and understandable, introductory level courses and textbooks frequently present concepts that are technically correc

细胞组织消化常用的几种酶的选择

直接从生物体获取的组织,一般需要将其消化成单个细胞才能进行体外培养。这种直接从离体组织获得的细胞,更接近于生物体内的生活状态,且生物性状尚未发生很大改变,因此在药物筛选、细胞移植、类器官培养、肿瘤研究等众多领域备受欢迎。但组织消化过程中常遇到多种问题,例如消化不完全、细胞死亡率高等。如何克服这些问题

如何用流式细胞仪检测线粒体数量

可以参考Mattiasson, G. (2004). "Flow cytometric analysis of isolated liver mitochondria to detect changes relevant to cell death." Cytometry A 60(2): 145-

Isolate-DNA-from-NRBC-Blood-from-Buccal-Swab-collected-with-filter-paper

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

检测细胞凋亡的实验方法比较5

3 胆汁淤滞性肝病在许多临床综合征中可以观察到胆汁淤滞,胆汁淤滞是一组慢性进行肝病的主要特征,并可最终导致肝硬化、肝衰竭和死亡。肝内疏水的毒性胆盐储滞长期以来被认为是肝损伤的一个主要原因,并被认为是胆汁淤滞性肝病肝损伤的一个关键原因。事实上肝内毒性胆盐:鹅脱氧胆酸和脱氧胆酸盐的储滞水平与肝损伤的程度

Midiprep-preparation-of-Plasmid-DNA

实验概要The  PureLink™ HiPure Plasmid DNA Midiprep Kit allows purification of  100–350 μg of high-quality plasmid DNA from 15–25 mL overnight E. coli  cul

Protocols-for-LCM-preparation-and-analysis

Protocols for LCM preparation and analysis I. Preparation, LCM and RNA/DNA extraction of Frozen Tissue SectionsA. EmbeddingB. CuttingC. StainingII. Pr

Preparation-of-tubulin2

DAY 2: Cycling preparation of MT protein.Keep the brains in an evacuated plastic ziplock bag buried in ice from the time of slaughter during transport

Tissue-preparation-protocol-for-ChIP

实验概要This protocol  describes how chromatin is prepared from tissue, which can subsequently  be used for chromatin immunoprecipitation (ChIP). It is re

Maxiprep-preparation-of-Plasmid-DNA

实验概要The  PureLink™ HiPure Plasmid DNA Maxiprep Kit allows purification of  500–850 μg of high-quality plasmid DNA from 100–200 mL overnight E. coli cu

Preparation-of-nucleic-acid-probes

Preparation of nucleic acid probesIn standard nucleic acid hybridization assays the probe is labeled in some way. Nucleic acid probes may be made as s

Preparation-of-Sonicated-Human-DNA

Purpose:To break up high molecular weight human placental DNA into fragment sizes of 500 bp or less which can be used as competitor DNA in Southern an

Large-Scale-Tubulin-Preparation

Tubulin is purified from bovine/porcine brain by two cycles of polymerization/depolymerization followed by removal of copurifying proteins on a phosph

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

Preparation-of-Lactobacillus-Competent-Cells

OverviewInstructions on how to prepare Lactobacillus plantarum competent cells before electrotransformation.MaterialsMRS mediaCulture of L. plantarum 

Preparation-and-Staining-of-Paraffin-Sections

I. Fixation and Processing of Tissue for Paraffin SectionsA. Fixation of Tissues in 10% Neutral Buffered FormalinSacrifice animal by prescribed and ap

Blood-Smear:-Preparation-and-Staining

Blood Smear: Preparation and StainingReference:Davidson, I. and Henry J., Clinical Diagnosis by Laboratory Methods, I. Davidsohn and J. Henry, eds., W

DNA微序列技术

·         Protocols for Making Drosophila Arrays (Stanford U.)Detailed protocol for making arrays including PCR Amplification of cDNAs for Printing, 

Decontamination-of-cells-from-the-yeast

I     Destroy yeast1.     Aspirate medium and wash cell in PBS.2.     Incubate cells at 37oC for 5 min in non-diluted antibiotic-antimycotic.3.     In

PCR-from-Plant-Tissue

1.protocol(1)collect piece of tissue (e.g., pieces of a leaf or flower) in Eppendorf tube containing 40 ml 0.25 N NaOH(2)put in boiling H2Ofor 30 sec

DNA-Extraction-from-Tissue

实验概要DNA extraction from tissue.主要试剂Extraction buffer100 mM Tris-HCl (pH 8.0)     100 mM EDTA (pH 8.0) 100 mM Na-Phosphate (pH 8.0)   1.5 M NaCl1% CTAB

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

PCR-from-Plant-Tissue

PCR from Tissue Reference:  Klimyuk et.al., 1993, Plant J. 3:493-494 Last updated: 1/27/00 By: Kay Schneitz        collect piece of tissue (e.g., piec

ISOLATION-OF-RNA-FROM-BACTEROIDS

3 g nodules (fresh or frozen in liquid N2) were ground to a powder in mortar and pestle with liquid N2. To the powder was added ice cold 0.5 M mannito

Plasmid-isolation-from-yeast

Pick colonies into 0.5ml of SD-Leu (or other appropriate SD medium)Vortex for 1minLeave to grow O/N for 18-24h at 30°C, 230-250rpm (best in 5ml bijou)

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

JC1分析线粒体膜电位的方法

Analysis of Mitochondrial Membrane Potentialwith the Sensitive Fluorescent Probe JC-1 Andrea Cossarizza and Stefano Salvioli Department of Biomedical

Culturing-Rat-Fetal-Neural-Stem-Cells

实验概要Rat  neural stem cells (NSCs) serve as a well-established model for  investigating human brain development, disease processes, and treatment  stra

Largescale-Immunocytology

This protocol describes our method for preparing cells for immunofluorescence, in which all incubations and washes are performed in microtiter dishes.

Derivation-and-Culture-of-Cortical-Astrocytes

实验概要Astrocytes are the  most numerous cell type in the central nervous system (CNS). They play  critical roles in adult CNS homeostasis, provide bioch