-
铜绿假单胞菌
铜绿假单胞菌 一、菌种简介1、菌种名称：铜绿假单胞菌 Pseudomonas aeruginosa2、菌种编号：B813193、菌种原始编号：ATCC90274
2024-11-13 123 -
Degenerate Primers
Degenerate PrimersFor amplification of cognate sequences from different organism
2024-11-13 53 -
Colony PCR
Colony PCR David Amberg This procedure will work for both yeast and E. coli:Take
2024-11-13 58 -
Multiplex PCR
Multiplex PCR is a variant of PCR which enabling simultaneous amplification of m
2024-11-13 55 -
Polymerase Chain Reaction (PCR) to Amplify rRNA Gene Fragment
Polymerase Chain Reaction (PCR) to Amplify rRNA Gene Fragment Prepare sufficient
2024-11-13 49 -
PCR基本实验方法（二）
Recommended Reaction Conditions: Initial Conditions:Initial denaturation at star
2024-11-13 87 -
PCR clean up using 3M sodium acetate and chilled absolute ethanol
For each 20 ul of PCR product, prepare the following mixture in 1.5 ml Tube.2 ul
2024-11-13 49 -
Degenerate PCR Detailed guide
Degenerate PCR by Michael Koelle The identification of novel members of gene fam
2024-11-13 45 -
Differential Display of Cotton Transcripts
Plant MaterialsCotton ovules (Gossypium hirsutum cv. Coker 312) were collected 8
2024-11-13 128 -
PCR的下游应用
・ Agarose Gel Electrophoresis of PCR Products (Robert H. Cruickshank)・
2024-11-13 71 -
PCR Technology
Introduction Polymerase chain reaction (PCR) has rapidly become one of the most
2024-11-13 60 -
Troubleshooting for PCR and multiplex PCR
Troubleshooting for PCR and multiplex PCRTroubleshooting discussion is based on
2024-11-13 53 -
PCR Primers For Gene Expression Detection or Quantification
Why PrimerBank?PrimerBank is a public resource for PCR primers. These primers ar
2024-11-13 47 -
CGH of PCR Amplified Microdissected DNA
PCR:We generally use 1-2 ul of starting paraffin microdissected DNA for each 50
2024-11-13 53 -
Primer Design Rules for Bisulfite Conversion Based PCR
Primer Design Rules for Bisulfite Conversion Based PCRAuthor: Long-Cheng LiSourc
2024-11-13 56
