Raturinarybladderurothelialcells

1. Bladders were excised from deeply anesthetized (urethane, 1.2 gm • kg−1, i.p.) Sprague Dawley rats (of either sex), cut open, and gently stretched (urothelial side down). 2. Anesthesia was determined to be adequate for surgery by periodically testing for the absence of a withdrawal reflex to a strong pinch of a hind paw and absence of an eye-blink reflex to tactile stimulation of the cornea. 3.......阅读全文

Rat-urinary-bladder-urothelial-cells

1. Bladders were excised from deeply anesthetized (urethane, 1.2 gm • kg−1, i.p.) Sprague Dawley rats (of either sex), cut open, and gently stretc

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

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

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

ThymidineIncorporation-Assay-for-Rat1a-cells

Thymidine-Incorporation Assay for Rat-1a cells      Overview   This method of Peter Coward, Ph.D. in the Conklin Lab was used in Coward, et al (1998)

Sleeping-Beauty-transposon-mutagenesis-in-rat-spermatogonial-stem-cells

Sleeping Beauty transposon mutagenesis in rat spermatogonial stem cellsZoltán Ivics,1, 2 Zsuzsanna Izsvák,1, 2 Gerardo Medrano,3, 4 Karen M Chapman3,

Isolation-and-culture-of-SpragueDawley-rat-aortic-smooth-muscle-cells

The intact mature arterial media is composed of at least four phenotypically unique cell subpopulations that reside in distinct medial layers.  Th

[3H]ThymidineIncorporation-Assay-for-Rat1a-cells

Overview This method of Peter Coward, Ph.D. in the Conklin Lab was used in Coward, et al (1998) Controlling signaling with a specifically designed Gi-

A-primary-cell-culture-model-of-rabbit-uroepithelium

Isolation of Epithelial Cells from Rabbit Bladders 1. Animal experiments were performed in accordance with the Animal Use and Care Committee. 2. Urina

尿液诊断膀胱癌的研究进展(二)

3.2 细胞成分检测 3.2.1 生存素( survivin) 生存素是凋亡抑制蛋白,在多种人类肿瘤中均可上调。研究发现尿液标本中生存素水平检测总的敏感度、特异度、阳性和阴性预测值分别为64%、93%、92%和67% [16],这些指标均优于传统的尿液细胞学检查和NMP22检测,且尿液中

Global-urinary-metabolic-profiling-procedures-using-gas-chromatography

Global urinary metabolic profiling procedures using gas chromatography–mass spectrometryEric Chun Yong Chan,1 Kishore Kumar Pasikanti1, 2 & Jeremy K N

Rat-Lung-Perfusion

实验概要The procedure presented below describes a method for perfusing rat lung.主要试剂Phosphate Buffered Saline主要设备1.Dissecting Microscope or Eye Magnifier2

Rat-Liver-Preparation

实验概要The procedure presented below describes a method for preparing rat liver.主要试剂1.      Aluminum Foil2.      Liquid Nitrogen3.      Dry Ice4.      Ph

膀胱癌研究体内外模型综述(一)

膀胱癌是泌尿生殖系统最常见的恶性肿瘤之一,在我国其发病率及病死率均列泌尿生殖系统肿瘤的首位。 2015年全国新确诊为膀胱癌的患者人数超过8万,导致的死亡人数超过3万,约70%以上首诊时是浅表性癌。膀胱癌的高复发率和治疗后期的并发症是临床治疗的两大难题。深入研究膀胱癌的发病机制、发展过程及转移规律

Rat-Blood-Collection-Protocols

实验概要The procedure presented below describes a method for collecting rat blood.实验步骤Rat should be fully anesthetized (e.g., unresponsive to toe pinch).1

Culture-of-BEND-Cells-(Bovine-Endometrial-Cells)

Culture of BEND Cells (Bovine Endometrial Cells)Charles E. Krininger, III and Peter J. Hansen Dept. of Animal Sciences, University of FloridaThis prot

Differentiate-ES-cells-into-glial-cells-and-neurons

Day -1: Pass ES cells at normal density on gelatinized plate to free the culture of contamination fibroblast cells.___________________Day 1: Trypsiniz

科学家发现膀胱癌干细胞起源的重要遗传学机制

  肿瘤干细胞在肿瘤细胞的发生、自我更新、耐药性和转移中扮演着重要角色。作为泌尿系统最常见的恶性肿瘤——膀胱癌干细胞(Bladder Cancer Stem Cells)的起源和遗传学基础目前仍不明确。  中国科学院生物物理研究所蛋白质科学研究平台抗体工程实验室李翀与中国科学院微生物研究所、深圳大学

Differentiating-Neural-Stem-Cells-into-Neurons-and-Glial-Cells

实验概要The protocols in  this section describe the steps involved in differentiating neural stem  cells (NSC) to neurons, astrocytes, and oligodendrocyte

膀胱癌研究体内外模型综述

  膀胱癌是泌尿生殖系统最常见的恶性肿瘤之一,在我国其发病率及病死率均列泌尿生殖系统肿瘤的首位。 2015年全国新确诊为膀胱癌的患者人数超过8万,导致的死亡人数超过3万,约70%以上首诊时是浅表性癌。膀胱癌的高复发率和治疗后期的并发症是临床治疗的两大难题。深入研究膀胱癌的发病机制、发展过程及转移规律

RAT/MOUSE-GROWTH-HO...

实验概要This  Rat/Mouse Growth Hormone ELISA kit is used for the non-radioactive  quantification of Growth Hormone in rat or mouse serum, plasma, tissue  

Histopathological-Approach-to-Rat-Liver-Tissue

ProcedureAfter deep ether anesthesia, dissect the rat’s liver (Wistar albino rats, 200 – 250 g) by cutting on the ventral side.Fix 2 – 3 mm. of the li

Immunofluorescent-Staining-of-Mouse-and-Rat-Leukocytes

I. ProcedureHarvest cells from tissue, preparing a single cell suspension. Red blood cells may be removed by lysis or density gradient: Red blood cell

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

Isolation-of-rat-cardiac-fibroblasts-and-cardiomyocytes

1. Hearts were removed from newborn rats (day 0), put into calcium- and bicarbonate-free HEPES-buffered Hanks’ medium, cut into pieces and digeste

Preparing-Mitochondria-from-Rat-Liver

Liver is a convenient source for functional intact mitochondria for a number of reasons. Animal tissue is more readily homogenized than plant tissue b

Preparation-of-Mitochondria-from-Rat-Liver

Preparation of Mitochondria from Rat LiverRat liver is an ideal source for functional intact mitochondria for a number of reasons. We use Sprague-Dawl

Growing-cells

No two cell lines behave exactly the same, so you must learn the peculiarities, or personality, of each of the cell lines with which you work. Irrespe

Freezing-Cells

1) Keep prepared solutions on ice.2) Determine total cell count of cells to be frozen. (e.g. 1 X 108 )3) Determine number of vials to be frozen. (e.g.

Lyophilizing-Cells

Lyophilizing CellsInoculate 200 ml L-broth supplemented with appropriate antibiotics with the bacteria to be lyophilized.Incubate the culture at 37°C