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Top : New Forum Archives (2009-): : Molecular-Biology
91. Gel doubling banding and resolution problem - (reply: 6)
92. Cant get rid of DNA contamination in RNA - (reply: 2)
93. PCR DNA bands too large on agarose gel - (reply: 1)
94. Easy to transfect primary cell line? - (reply: 1)
95. Sequence specific pulldown of dsDNA - (reply: 8)
96. Gene expression and transcription factors - (reply: 1)
97. RNA gel problem (melted bands) - (reply: 2)
98. RNA extraction and DNase treatment - (reply: 1)
99. Cloning purified PCR product into cells - (reply: 5)
100. Mention of Transgene Insertion into Cell Lines By Transfecting with cDNA - (reply: 2)
101. when to add polybrene for lentivirus transduction? - (reply: 1)
102. How to know the plasmid extracted are indeed the plasmid of interest? - (reply: 4)
103. In situ hybridization - (reply: 5)
104. Sypro Ruby Dye Front - (reply: 9)
105. Forced Expression vs. Enforced Expression - (reply: 1)
106. Co-immunoprecipitation non-specific binding - (reply: 2)
107. New webpage and software tools - (reply: 1)
108. What DCH5a cells are? / pCAMBIA1301 isolation from DHC5a cells - (reply: 3)
109. Can I snap freeze my tissue (liquid nitrogen) in Lysis buffer for later RNA extr - (reply: 6)
110. Gateway cloning not working. - (reply: 7)
111. Assays from very few number of cells - (reply: 1)
112. EM7 promoter - what is it? - (reply: 1)
113. Virus processing (filtration) of blood - How to? - (reply: 5)
114. ABC(D) Model of Plant Flowers - (reply: 1)
115. TE buffer pH adjustment - (reply: 1)
116. Estimate cost for Molecular Docking software/devices - (reply: 1)
117. Polymorphism - (reply: 2)
118. PCR_QUALITY CONTROL - (reply: 2)
119. Difficult cloning/ligation/transformation blunt and sticky - (reply: 1)
120. TOP10F Chemically Competent E. coli - (reply: 1)