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Terminal deoxynucleotidyl Transferase-mediated dUTP nick end labeling (TUNEL) is an in situ method for detecting the 3'-OH ends of DNA exposed during the internucleosomal cleavage that occurs during a ...

Detection of Alu by PCR In this experiment polymerase chain reaction (PCR) is used to amplify a nucleotide sequence from chromosome 8 to look for an insertion of a short DNA sequence called Alu ...

Protocol for Paraffin Sections: Dewax paraffin sections: Incubate slides 55°C 30 min. Xylenes 2 times 2 min. each 100% EtOH 2 times 2 min. each&nb ...

Protocol I: Triton X-100 Lysis Buffer In 96 flat-wells plate incubate 4x10 6 target cells (40 wells of 105 per well) with desired concentration of effectors (105 target cells per well). After incubat ...

Designing PCR programs 1Basic Principles The requirement of an optimal PCR reaction is to amplify a specific locus without any unspecific by-products. Therefore annealing needs to take place at a suff ...

Materials from a workshop held March 1997 in Modena Italy. All materials reproduced with permission. Introduction A. Cossarizza Workshop Sponsors Methods in analysis of apoptosis and cell necrosis. Z. ...

BrdU Incorporation Protocol Day 1 Label cells with media containing100 μM BrdU (6 μL/mL of 5 mg/mL stock): Diploid Fibroblasts 4-6 hours ES cells 30 minutes 3T3 cells 2.5 hours Trypsinize ce ...

immunofluorescence labeling; that is the antibodies have the fluorescent dye attached. Direct labeling is simpler and quicker than indirect labeling. We strongly recommend direct labeling if you're pl ...

FIXATION and DNA Staining for Cell Cycle Analysis BackgroundThis method of DNA staining utilizes ethanol to fix the cells and permeabilize the membrane which allows the dye (Propidium Iodide) to enter ...

A method to re-PCR unique bands from products of mixed size INTRODUCTION The products of a PCR reaction - especially when this is done on eukaryotic genomic DNA and when using degenerate ...

Paraformaldehyde Fixation of Cells BackgroundThis fixation method is good for cells labelled by fluorochrome-conjugated antibodies to membrane antigens. It will stabilize the light scatter and labelli ...

Fixation 1) Collect 2 X 106 cells. 2) Pellet cells by spinning at 1000 rpm 4°C for 5 minutes. 3) Resuspend cell pellet in 1 ml of cold PBS. 4) Fix cells by adding 4 ml of -20°C absolute ethano ...

Colony PCR This procedure will work for both yeast and E. coli: Take a small colony and suspend it in 5ul of H2O in a PCR tube. Heat for 5 min at 95℃ and then spin the condensation down ...

Choosing/designing PCR primers In designing primers for PCR the following steps/rules were tested and proven to be useful: 1Length of individual primers between 18-24 bases. Longer primers (30-35 bp) ...

CGH of PCR Amplified Microdissected DNA PCR: We generally use 1-2 ul of starting paraffin microdissected DNA for each 50 ul DOP-PCR reaction. We assume that about 1 ug of product is produced in each D ...

停产，用次氯酸钠将房间整个清洁消毒，所有器具高温灭菌或用次氯酸钠浸泡。 地面用量：有效氯浓度2500ppm，大于30min； 器具：有效氯浓度500ppm，20min。摇床用甲醛加高锰酸钾熏蒸，用前再用紫外照射半小时。 发酵罐高温灭菌。 如果空气中噬菌体浓度也较高的话，可以用甲醛熏蒸，3g/平米；或用紫外照射，但要注意，因为这两种方法都可能对仪器造成腐蚀。下水也要用次氯酸钠处理。空气中噬菌体的检测 ...

1 样品采集 将一定的样品放入灭菌三角瓶中，加入对数生长期的敏感指示菌如大肠杆菌菌液3～5mL，再加20mL二倍肉汤蛋白胨培养液。 2 增殖培养 30℃振荡培养12～18h 使噬菌体增殖。 3 离心分离 将上述培养液以3000rpm离心15～20min 取上清液，用pH7.0，1%蛋白胨水稀释至10-2～10-3，用于噬菌体检查及效价测定。 4 生物测定法 4.1双层琼脂平板法 4.1.1 倒下层 ...

Calculating Concentrations for PCR a) Primers: i) Oligonucleotide primers are generally supplied as "so many OD units/ml" - but what does this mean in terms of mg/ml or mmol/ml etc? & ...

噬菌体： M13KE T7 宿主细胞 ： ER2738 BL21/BLT5403/BLT5615 噬菌体释放方式： M13噬菌体溶源性，不裂解宿主菌。极大地简化了每轮淘选过程中的噬菌体纯化步骤，只用简单的PEG沉淀方法即可。 T7是裂解性的，其展示的蛋白不需分泌。这一优点使更多的序列可能被展 ...

"BEST" PCR conditions for amplifying DNA from plasmids 1PCR reaction system: 25 ng linear template (~6.5 kb) 50 pmol each primer 100 pmol each dNTP 1X Promega Taq buffer (no Mg2+) 1.5 mM Mg ...