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Laboratory Protocol
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Southern Blotting More >>
Electrophoresis of DNA is carried out in a neutral agarose gel system. Prepare a 0.8-1% agarose gel containing 1x TAE buffer. Ethidium bromide can be added to ... /     United States
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Protocol for intracytoplasmic staining of cytokin... More >>
Prepare spleen, lymph node or T cell clone cells as single cell suspension, using erythrocyte lysis (water) or Lymphopaque as appropriate. /     United States
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Conjugation of monoclonal antibodies More >>
In this series of web pages, protocols, notes, and various illustrations are given to aid in the conjugation of proteins--principally monoclonal antibodies--to... /     United States
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Microbiology - Replica Printing More >>
Sterilize velvet squares with widths at least 50% longer than the diameter of a Petrii plate. /     United States
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Inverse PCR for PAC-end sequencing More >>
Goal is to generate PCR fragments that contain the ends of PAC inserts that can be sequenced. For inverse PCR we cut the PAC once in the vector (near outward ... /     United States
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Chromatin Immunoprecipitation (ChIP) of Protein C... More >>
This protocol describes the use of chromatin immunoprecipitation technology (ChIP) to analyze interactions of proteins or protein complexes with DNA in vivo. /     United States
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Chemical Modificaiton of Proteins and Peptides More >>
Amino groups of proteins are basic groups (pK values near 8 for α-NH2 and 9.5 for ε- NH2) and are positively charged except at high pH. /     United States
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Tissue Fixation and Staining Techniques More >>
Deparafinize - 100%, 95%, 80%, 70%, 50%, 30% ETOH, H20 (10 dips each) /     United States
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Cell Culture More >>
Remove ligament from animal using as sterile technique as possible. A one inch segment from an older 270 day old fetus will be more than sufficient. /     United States
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Immuno Techniques More >>
In mildly acidic conditions, the addition of short-chain fatty acids such as caprylic acid to serum will precipitate most serum proteins with the exception of... /     United States
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