Lipidanalysis：EXTRACTIONOFLIPIDSFROMLIPOPHORIN
Lipid analysisEXTRACTION OF LIPIDS FROM LIPOPHORIN Since lipids are hydrophobic, they are better soluble in organic solvents than in water. Because the lipids are buried into protein particles simple shaking of the aqueous protein solution with an immiscible solvent will not lead to efficient extraction. The method of choice is a one phase extraction, as pioneered by Folch and modified by Bligh a......阅读全文
Lipid－analysis：EXTRACTION－OF－LIPIDS－FROM－LIPOPHORIN
Lipid analysisEXTRACTION OF LIPIDS FROM LIPOPHORIN Since lipids are hydrophobic, they are better soluble in organic solvents than in water. Because th
Phosphatidylinositol－4Kinase－and－Phosphatidylinositol－4Phosphate－5K...
Phosphatidylinositol 4-Kinase and Phosphatidylinositol 4-Phosphate 5-Kinase AssaysInositol lipid kinases are perhaps the easiest and most straightforw
LIPID－EXTRACTION
PROCEDURE1. Resuspend tissue/extract in 5 volumes of 1:1 chloroform/methanol by vortexing (to homogeneity or as close as possible)2. Add the same volu
Lipid－analysis
Thin layer chromatography is based on the separation of a mixture of compounds as it migrates with the help of a suitable solvent through a thin layer
Lowdensity－lipoprotein－(LDL)－pathway－during－atherogenesis
Low-density lipoprotein (LDL) is a plasma lipoprotein particle whose lipid component includes cholesterol and triglycerides and is commonly referred t
Glycosphingolipid－analysis
1) Incubate cells with 1 µCi/ml of 3H-galactose for 72 hours.---> If treatment is for an extended period of time: treat in serum free media containing
SREBP－control－of－lipid－synthesis
Sterol-regulatory element binding proteins (SREBPs) play a key role in transcriptional regulation of cholesterol metabolism in response to cholesterol
Reversal－of－Insulin－Resistance－by－Leptin
The insulin resistance of type II diabetes appears to be caused in part by the presence of high levels of lipids in cells such as skeletal muscle wher
Lipid－analysis－Week－3:－GAS－LIQUID－CHROMATOGRAPHY
During this week, you will analyze the fatty acid composition of the individual lipid fractions recovered from the TLC plate. Gas chromatography is a
Nuclear－Receptors－in－Lipid－Metabolism－and－Toxicity
Nuclear receptors are transcription factors that are activated upon binding to its ligands. Initially, they had been classified as classic endocrine n
Sphingomyelin－Mass－Measurement
Protocol:Bligh & Dyer extraction1) Pellet approximately 1 X 107 cells.2) Resuspend pellet in 3 ml CHCl3: CH3OH (1:2) and vortex hard.3) Add 0.8 ml H2O
Phosphoinositides－and－their－downstream－targets.
Nine currently identified phosphoinositide 3-kinases (PI 3-K) constitute a subfamily of lipid kinases that catalyze the addition of a phosphate molecu
Realspace－and－realtime－dynamics－of－CRISPRCas9－visualized－by－...（四）
Fig. 6HS-AFM observations of the non-specific transient binding of Cas9–RNA. a Sequential HS-AFM images of Cas9–RNA molecules transiently bound to
Lipoprotein－Analysis－Week－2:－Electrophoresis2
Preparation of stacking gelPrepare a 7.5 ml of 3% stacking gel in a small beaker using the following amounts of appropriate reagents.Stockfinal conc.A
Determination－and－Detection－of－Reactive－Oxygen－Species－(ROS),－Lipid－...
Reactive oxygen species or intermediates are formed by the incomplete reduction of oxygen. Organisms living in aerobic environment generate variou
大鼠血脂（Lipids）ELISA试剂盒使用说明
实验原理：本试剂盒应用双抗体夹心法测定标本中大鼠血脂（Lipids）水平。用纯化的大鼠血脂（Lipids）抗体包被微孔板，制成固相抗体，往包被单抗的微孔中依次加入血脂（Lipids），再与HRP标记的血脂（Lipids）抗体结合，形成抗体-抗原-酶标抗体复合物，经过彻底洗涤后加底物TMB显色。TMB
PCR－from－Tissue
collect piece of tissue (e.g., pieces of a leaf or flower) in Eppendorf tube containing 40 ml 0.25 N NaOHput in boiling H2 O for 30 sec (optimum may n
PCR－from－Tissue
collect piece of tissue (e.g., pieces of a leaf or flower) in Eppendorf tube containing 40 ml 0.25 N NaOHput in boiling H2O for 30 sec (optimum may ne
PCR－from－Tissue
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 H2O for 30 sec (optimum
Lipoprotein－Isolation－－First－week
As insects have an open circulatory system, the hemolymph can be simply collected through an incision in the body wall. Most conveniently, you should
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
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
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
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
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
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
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
Lipid－analysis－Week－3:－GAS－LIQUID－CHROMATOGRAPHY2
B: GLC procedureThe GLC will be prepared for your use. Please do not attempt to turn on the GLC on your own if it is off. Do not change any of the set