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