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Top : New Forum Archives (2009-): : Molecular-Biology
91. Troubleshooting with cloning - (reply: 2)
92. qPCR acceptable standard deviation - (reply: 1)
93. Gel doubling banding and resolution problem - (reply: 6)
94. Canīt get rid of DNA contamination in RNA - (reply: 2)
95. PCR DNA bands too large on agarose gel - (reply: 1)
96. Easy to transfect primary cell line? - (reply: 1)
97. Sequence specific pulldown of dsDNA - (reply: 8)
98. Gene expression and transcription factors - (reply: 1)
99. RNA gel problem (melted bands) - (reply: 2)
100. RNA extraction and DNase treatment - (reply: 1)
101. Cloning purified PCR product into cells - (reply: 5)
102. Mention of Transgene Insertion into Cell Lines By Transfecting with cDNA - (reply: 2)
103. when to add polybrene for lentivirus transduction? - (reply: 1)
104. How to know the plasmid extracted are indeed the plasmid of interest? - (reply: 4)
105. In situ hybridization - (reply: 5)
106. Sypro Ruby Dye Front - (reply: 9)
107. Forced Expression vs. Enforced Expression - (reply: 1)
108. Co-immunoprecipitation non-specific binding - (reply: 2)
109. New webpage and software tools - (reply: 1)
110. What DCH5a cells are? / pCAMBIA1301 isolation from DHC5a cells - (reply: 3)
111. Can I snap freeze my tissue (liquid nitrogen) in Lysis buffer for later RNA extr - (reply: 6)
112. Gateway cloning not working. - (reply: 7)
113. Assays from very few number of cells - (reply: 1)
114. EM7 promoter - what is it? - (reply: 1)
115. Virus processing (filtration) of blood - How to? - (reply: 5)
116. ABC(D) Model of Plant Flowers - (reply: 1)
117. TE buffer pH adjustment - (reply: 1)
118. Estimate cost for Molecular Docking software/devices - (reply: 1)
119. Polymorphism - (reply: 2)
120. PCR_QUALITY CONTROL - (reply: 2)