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Top : New Forum Archives (2009-): : Molecular-Biology
61. qPCR and miRNA isolation - (reply: 4)
62. Yeast Two Hybrid system - (reply: 6)
63. how much purify protein nedded for IP - (reply: 9)
64. lyophilized protein dilution - (reply: 6)
65. Do homologous arms need to overlap right at the DSB for knock-in - (reply: 1)
66. Is it possible quantify dsDNA pre-sequencing with a kit in stepone plus qpcr - (reply: 2)
67. finding a reference for a formula - (reply: 2)
68. CHO-K1 transfection problem - (reply: 1)
69. Not Template Control Contamination - (reply: 7)
70. Mesenchymal stem cells Expressing BDNF - (reply: 5)
71. Problem with Site-directed mutagenesis of a 9 kb template with high GC content ( - (reply: 3)
72. How to do a primer dilution - (reply: 10)
73. Can I use an EtBr stained PAGE gel for northern blot? - (reply: 2)
74. gDNA still presents even after DNase treatment - (reply: 6)
75. help interpreting this data - (reply: 2)
76. 293t transfected with prtTA inducible vex - (reply: 5)
77. RNA contamination in plasmid extracted - (reply: 1)
78. 0.2 vs 0.45um filter for clearing retro- or lentiviral supernatant? - (reply: 2)
79. PCR and sequencing of genomic DNA - (reply: 4)
80. Virus sample - (reply: 3)
81. NESTED PCR - (reply: 6)
82. Electroporation query - (reply: 7)
83. Failed cloning - different readings - (reply: 10)
84. mRNA copies of each gene under different promoters - (reply: 1)
85. Purified DNA fragments are bigger than unpurified - (reply: 2)
86. Phoenix Amphoteric cell line to package lentivirus? - (reply: 6)
87. Digestion necessary after PCR? - (reply: 7)
88. Merodiploids on sucrose plates? - (reply: 1)
89. Inverse PCR product selection - (reply: 2)
90. Dead cells after transfection - (reply: 8)