cDNA/AFLPProtocol

Preparation of Para-magnetic beads from Promega cat#Z5482:a) suspend magnetic particles in bottle - transfer 200 ul (200 ug) of beads per sampleof RNA to be purified to a microfuge tube or tubes.b) place microfuge tube in magnetic stand for 30 sec or longer to collect the beads.c) remove supernatent and wash 3X with 200 ul of 0.5X SSCd) finally resuspend the SA-PMPs in 100ul of 0.5X SSC for each 2......阅读全文

ELISPOT-Protocol

实验概要The  Elispot (Enzyme Linked Immuno-Spot) assay provides an effective method  of measuring the antibody or cytokine production of immune cells on t

ELISPOT-protocol

实验概要The procedure  below is a general guideline procedure for ELISPOT. Abcam ELISPOT kits  have been designed for detection of various cytokines and g

NAi-protocol

siRNA protocolsOur current strategy with siRNA is to synthesis relatively small amounts enzymatically and use these to test for efficiency by western

ELISPOT-Protocol

实验概要The  Elispot (Enzyme Linked Immuno-Spot) assay provides an effective method  of measuring the antibody or cytokine production of immune cells on t

Immunoprecipitation-Protocol

实验概要Immunoprecipitation  is a procedure by which proteins or peptides that react specifically  with an antibody are removed from solution and examined

PCR-protocol

PCR reactionProtocol for 50µl reaction - adjust amounts if necessary, for a 20µl reaction use the same volumes of primer and dNTP-mix, but adjust the

RLGS-protocol

A. Preparation of DNA SolutionIn the case of rice, for example    This method may be appllicable for many grass species and some other plants.        

RNAi-protocol

 siRNA protocolsOur current strategy with siRNA is to synthesis relatively small amounts enzymatically and use these to test for efficiency by western

Immunoblot-Protocol

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

ELISA-protocol

ELISA protocol:1.取5-10ul BMMY表达上清用0.05M NaHCO3稀释到100ul铺ELISA板,37度或室温振荡大于1小时。注意一定要做一个GS115空菌株表达上清作为阴性对照,最好还找一个带有histag的蛋白作为阳性对照。2.TPBS洗板3次,方法:倒掉铺板液,倒置于

Transformation-Protocol-for-Arabidopsis

Transformation Protocol for Arabidopsis – Abbreviated Germinate seed in pots ↓ 4 weeks Streak bacteria onto YM/MinA ↓ 2-3 days 28°C Spray/dip ba

Silver-Staining-Protocol

1x 40min - overnight     50% MeOH, 12% Acetic Acid 1x 30min                                  50% MeOH, 12% Acetic Acid, 0.05% 37% Formaldehyde 3x 2

Immunofluorescence-Microscopy-Protocol

实验概要 Immunofluorescence  allows the imaging of a specific factor in cells or tissue sections  through the use of a specific antibody chemically whic

RNA-Isolation-Protocol

RNA Isolation Protocol(Revised 5-15-2003)Stabilize RNAStart with 15 ml E. coli Culture containing 7.5* 109 cells (OD600= 0.2 Dilute cells or scale up)

Yale-Immunofluorescence-Protocol

实验概要We provide a protocol for fixation, immunostaining, and imaging in 384-well Plates.主要试剂Reagents1. 384-well view plates (Aurora)2. HUVEC (pooled, L

Protocol-for-Cell-Fusion

Healthy Sp2/0 cells should be rapidly growing by this time. Sp 2/0 cells should be started about two weeks before the cell fusion. Every two days, the

Tissue-Harvest-Protocol

TISSUES TO BE PROCURED(minimally and preferably within 5-8 hours after death):1. Brain2. Liver3. Muscle4. Skin5: Others as the specific case dictatesP

BrdU-Labeling-Protocol

实验概要The thymidine analog, 5-bromo-2-deoxyuridine (BrdU),is a common reagent used for cell proliferation assays and for the detection of apoptotic

Cell-Extraction-Protocol

实验概要Primary tissues  are valuable tools for the study of intracellular and extracellular  markers which characterize disease states. We have developed

Colony-PCR-Protocol

1. Pull out eight glycerol stock plates from the –80oC freezer and set on bench top to thaw. Be sure to remove the foil seal before leaving the plates

Immunofluorescence-Microscopy-Protocol

实验概要Immunofluorescence  allows the imaging of a specific factor in cells or tissue sections  through the use of a specific antibody chemically which i

Protocol-for-dsRNA-Synthesis

实验概要        We routinely produce dsRNA by in vitro transcription of a PCR generated DNA template containing the T7 promoter sequence on both ends

Phycoerythrin-conjugation-protocol

Phycoerythrin conjugation protocolDavid's method modified from references (2) and (3). I used this method to conjugate a mouse IgG2a monoclonal an

Microarray-Hybridization-Protocol

Introduction:One microarray set consists of 7 nylon membranes with 2.5 x 7.5 cm dimension. 2304 genes were spotted onto nylon membranes (Schleicher an

Bacteria-Culture-Protocol

Bacteria Culture ProtocolBy 徐晓政1、TBS Medium Preparation:Prepare 1L of TBS medium contains:Tryptone 12gYeast extract 24gNaCl 5gSodium Succinate 5gGlyce

Protocol-for-Trichl...

实验概要The  efficiency of nucleotide incorporation in DNA/RNA polymerization  reactions (e.g. transcription, reverse transcription, and DNA  replication)

Nucleolar-Isolation-Protocol

We recommend that you first download and read this page as a PDF file. Using that as your guide, you can then follow the protocol below and view a Qui

Protocol-of-Northern-blot

Protocol of Northern blot质粒的转化和扩增质粒的鉴定目的基因片段的切割3.1样品双酶切(175μl水解体系)DW 115μlBuffer B(10×) 17.5μlBaM H 15μlPst I 17μlDNA(MMP-9) 16μlBSA 4.5μl37℃水浴,3h。3.2

Nuclear-Extraction-Protocol

实验概要The procedure presented below describes a method for extracting nuclear from several cell lines of human origin.主要试剂Hypotonic Buffer Solution20 mM

cDNA/AFLP-Protocol

Preparation of Para-magnetic beads from Promega cat#Z5482:a) suspend magnetic particles in bottle - transfer 200 ul (200 ug) of beads per sampleof RNA