SilverStainingProtocol

1x 40min - overnight 50% MeOH, 12% Acetic Acid1x 30min 50% MeOH, 12% Acetic Acid, 0.05% 37% Formaldehyde3x 20min &nbs......阅读全文

Silver-Staining-Protocol

1x 40min - overnight     50% MeOH, 12% Acetic Acid1x 30min                                  50% MeOH, 12% Acetic Acid, 0.05% 37% Formaldehyde3x 20min 

SSR-GEL-and-Silver-Staining-Protocol

I. EQUIPMENT:DNA sequencing unit (35 x 45 cm) & 2000V power supplyClampsLg. plastic trays (4), about 43 x 50 x 8 cm, and one lidTwo rocking platformsH

Intracellular-Staining-Protocol

1. Fix cells- Add16% formaldehyde directly into culture medium to obtain a final concentration of 1.5% formaldehyde.2. Incubate in fixative for 10 min

银染(silver-staining)操作规程

实验原理:在碱性条件下,用甲醛将蛋白带上的硝酸银(银离子)还原成金属银,以使银颗粒沉积在蛋白带上。染色的程度与蛋白中的一些特殊的基团有关,不含或者很少含半胱氨酸残基的蛋白质有时候呈负染。银染的详细机制还不是非常清楚。 试剂:乙醇、冰醋酸、乙酸钠、硫代硫酸钠、硝酸银、碳酸钠、甘氨酸或EDTA.Na

Actin-StainingActin-Staining-Protocol

实验概要Invitrogen  offers several fluorescent and biotinylated phalloidin and phallacidin  derivatives for labeling F-actin. These phallotoxins, isolated

Direct/Indirect-Staining-Protocol

Use this Protocol for Directly or Indirectly staining cells for Flow Cytometric Analysis1) Dilute cells to 5x10^6 cells/mL2) Aliquot 100uL of cells pe

Intracellular-Cytokine-Staining-Protocol

实验概要A  modification of the basic immunofluorescence staining and flow  cytometric analysis protocol can be used for the simultaneous analysis  of surf

Cell-Surface-Immunofluorescence-Staining-Protocol

实验概要A method of identifying  and enumerating specific cell types in a heterogeneous population of  cells by enhancing the specific staining of desired

Methylene-Blue-DNA-staining-protocol

Methylene Blue DNA staining protocolProtocol:Load 2-5X the amount of DNA that would give bands of moderate intensity on an ethidium bromide stained ge

Cell-Cycle-Staining-ProtocolDAPI

1. Harvest cells- wash 2X in PBS to get rid of serum proteins. 1200rpm, 5 min2. Resuspend pellet (up to 3x106 cells) in 1.2 ml PBS (Ca and Mg free).3.

Protocol-for-intracytoplasmic-staining-of-cytokines-for-FACS-analysis

DescriptionProtocol for intracytoplasmic staining of cytokines for FACS analysis Procedure1) Prepare spleen, lymph node or T cell clone cells as singl

蛋白质电泳

蛋白质电泳(主要内容如下)One-Dimensional SDS-PAGETwo-Demensional SDS-PAGEProtein Electrophoresis in Agarose Gel Gel StainingRecipesOne-Dimensional SDS-PAGE·      

低背景的蛋白质银染(silver-staining)方法

我们做蛋白质电泳的人都知道,银染色很灵敏,有很强的说服力,但通常胶背景较深,不易扫描。在这里介绍一下低背景的蛋白质银染方法。Step Reagent Time/minFix 50%EtOH, 12%HAC, 0.1%HCHO, 38%H2O 60Rinse 50% EtOH 5 min, 3 tim

蛋白质检测

·         Protein detection (Aberdeen's Lab)The method used to locate the proteins following 2D-PAGE depends on the nature of the original sample.

基因型分析

Randomly Amplified Polymorphic DNA (RAPD)Randomly Amplified Polymorphic DNA (RAPD) by  (DNA KAFFE)RAPD analysis has been successfully used in mapping

Silver-Acetate-Autometallography-(AMG)

In the early eighties, a series of papers were published by Gorm DANSCHER, Aarhus, Denmark, to introduce a reliable and easy-to-handle technique for l

Silver-Enhancement-...

实验概要The method provides a silver enhancement protocol for immunoassay.主要试剂Prepare the following reagents fresh daily except for the citrate buffer.1.

免疫细胞化学

Introduction to Immunocytochemistry (House Ear Institute)A brief overview of common available methods.  BrDU Immunocytochemistry using peroxidase and

Protein-Staining-Procedures

This method was successful in our lab using prostate tissue and for our specific objectives. Investigators must be aware that they will need to tailor

PVDF膜上蛋白的可逆染色

PVDF膜上蛋白的可逆染色   Western杂交时,为确认蛋白是否转至PVDF膜上,可用下列方法对膜上蛋白进行可逆性染色。1.      氨基黑染色染液:0.5% Amido Black (w/v), 25% isopropanol (v/v) and 10% acetic acid.染色:将PV

蛋白质电泳技术2

Decrease toxicity of destain even more!The destain procedure can be made even less toxic by replacing the destaining solution completely with MilliQ w

丙烯酰胺胶中肽提取和蛋白消化技术

Digestion of Proteins and Extraction of Peptides from an Acrylamide GelSherry Niessen, Ian McLeod and John R. Yates IIIDepartment of Cell Biology, The

组织学——包埋技术

Tissue Preparation for Methy Methacrylate EmbeddingMethyl Methacrylate Embedding Protocols (Energy Beam Sciences, Inc.)General protocol for plastic em

Silver:-Lysate-for-Western

Grow cellsHarvestSpin downWash with PBSSpin down enough cells to collect a 50-100 µL cell pellet in a FastPrep tubePrepare lysis buffer (beforehand) a

Silver:-Colony-PCR

Zymolyase Solution:Regular stock of zymolyase is 10 mg/ml diluted in water, mix by inverting, not all will go into solution (filter it) store aliquots

组织学——染色

Hematoxylin and Eosin Staining of Tissue for LCM (Arcturus)   Immunohistochemical Staining (IHC) (Arcturus)For optimal LCM from IHC samples, it is nec

Silver:-TimeLapse-Microscopy

Pad Preparation1. Microwave 2% agarose (mix of low-melt and normal, to taste) in Thorn media (see below). (If you have used different percentages of a

细胞遗传学——原位杂交(ISH)

In Situ Hybridization·         In Situ Hybridization (jsmith1@po-box.mcgill.ca)In situ hybridization, as the name suggests, is a method of localizing,

免疫组织化学

·         Double Peroxidase (HRP) Immunohistochemical Labeling of Trypsin-Sensitive Antigens (KPL)·         Immunohistochemistry (Tyner lab)This is a

peptide-fingerprint-mapping

Polyacrylamide gel electrophoresis is a widely used technique to separate proteins from biological samples. Moreover, the development of two-dimension