PreparingMitochondriafromRatLiver

Liver is a convenient source for functional intact mitochondria for a number of reasons. Animal tissue is more readily homogenized than plant tissue because there are no cell walls, and liver in particular is a soft and fairly homogeneous tissue. The metabolism of endotherms requires that some tissues maintain a high density of mitochondria, so the potential yield is high. Isolating mitochondria from highly structure......阅读全文

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

Isolation-and-characterization-of-rat-glomerular-endothelial-cells

Glomerular endothelial cells (GECs) from the kidney are in close juxtaposition to other cell types, such as mesangial cells, and may respond to as

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

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

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

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

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

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

Genomic-DNA-Extraction--PureLink™

实验概要The  PureLink™ Genomic DNA Purification Kit allows rapid and efficient  purification of genomic DNA. The kit is designed to efficiently isolate  g

线粒体荧光探针大全:TMRM,Mitotracker,JC1(1)

线粒体荧光探针信息大全 (Probes for Mitochondria)包括各种常用探针,如JC-1,JC-9,TMRM,TMRE等Mitochondria are found in eukaryotic cells, where they make up as much as 10% of th

Apoptotic-DNA-fragmentation-and-tissue-homeostasis

Apoptotic cell death can be triggered by many different cellular stimuli, resulting in activation of apoptotic signaling pathways including caspases (

流式应用精选——微核检测(体内体外)

 注:点击文章名称查看详情。文章名称样本仪器型号备注Assessment of the Genotoxic Potential of Azidothymidine in the Comet,Micronucleus, and Pig-a AssayBone Marrow and Peripheral

PriCells:-Questions

 Questions 1: Isolation of hepatocytes from other speciesThe basic two-step perfusion procedure can be used for obtaining hepatocytes from various r

Competitive-RTPCR-Strategy-for-Quantitative-Evaluation-3

Competitive RT-PCR in Different Tilapia TissuesAbundance levels of tiGHR I mRNA (target) in different tilapia tissues were measured using the quantita

Derivation-and-Culture-of-Dopaminergic-Neurons-(from-Midbrains-of-Rodents)

实验概要Dopaminergic  (DA) neurons are located in the ventral midbrain (VM). The ability to  isolate precursor cells and neurons from the VM provides a po

Apoptotic-Signaling-in-Response-to-DNA-Damage

The cellular activation of the caspase cascade resulting in cell death is triggered by chemical damage to DNA which stimulates a sequence resulting in

Lysosome-Isolation-in-Isotonic-Sucrose

LEVEL IMATERIALSRat liverPhysiological saline (0.85% w/v NaCl)0.25 M sucrose in 10 mM Tris-HCL, pH 7.4Brendler teflon homogenizerRefrigerated preparat

线粒体荧光探针大全:TMRM,Mitotracker,JC1(2)

MitoTracker Green FM ProbeMitochondria in cells stained with nanomolar concentrations of our patented MitoTracker Green FM dye (M7514) exhibit bright

Extraction-of-DNA-using-DNAzol®-Reagent

实验概要DNAzol®  Reagent (Genomic DNA Isolation Reagent) is a complete and ready-to-use  reagent for the isolation of genomic DNA from solid and liquid sa

Mitochondrial-Carnitine-Palmitoyltransferase-(CPT)-System

The oxidation of fatty acids is an important source of energy for ATP production in mitochondria through the entry of acetyl-CoA into the Krebs cycle.

Isolation-and-culture-of-rat-coronary-microvascular-endothelial-cells

CMVE were isolated from Wistar rat hearts by digestion of primary cell isolation kit.1. Hearts mounted on a Langendorff apparatus were perfused at 3

AbC™-AntiRat/Hamster-Bead-Kit

实验概要The AbC™  anti-Rat/Hamster Bead Kit provides a consistent, accurate, and  simple-to-use technique for the setting of flow cytometry compensation  

AbC™-AntiRat/Hamster-Bead-Kit

实验概要The AbC™  anti-Rat/Hamster Bead Kit provides a consistent, accurate, and  simple-to-use technique for the setting of flow cytometry compensation  

Differentiating-Glial-Precursor-Cells-into-Astrocytes-and-Oligodendrocytes

实验概要Glial  precursor cells (GPCs), also known as glial restricted progenitors  (GRP) or oligodendrocyte progenitor cells (OPCs), are cells that have  

Dissociation-of-Cells-from-Primary-Tissue

实验概要A  common method to obtain single cell suspensions from primary tissue is  enzymatic disaggregation. Expose the cells to enzymes for a minimal  am

The-salvage-pathway-from-serine-to-phosphatidylcholine

The biosynthesis of membrane phospholipids occurs through distinct pathways in mammals and bacteria. In the mammalian pathway for the synthesis of pho

Eccles:Protein-Lysates-from-Tissue

Cell Lysis Buffer5mL 0.1M Tris HCl pH 8 (10mM)0.44g NaCl (150mM)0.02g EDTA (1mM)0.5mL nonidet P40 (1% w/v)0.05g SDS (0.1% w/v)Make up to 50mL with MQH

Isolation-of-genomic-DNA-from-bacteria

Note: This procedure does not work well with Gram + cocci.Transfer 1.5 mL overnight culture to a 1.5 mL microfuge tube, centrifuge for 30 sec, decant