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Top : New Forum Archives (2009-): : Molecular-Biology
2071. Phenol chloroform ratio during RNA isolation - (reply: 1)
2072. Tris-acetate buffer? - (reply: 4)
2073. genomic dna isolated from blood is brown color?! - (reply: 4)
2074. problem with cloning PCR - can't amply the full-length cDNA with PCR (reply: 6)
2075. labeling dCTP, dATP, dGTP, dTTP - (reply: 2)
2076. Removal of RNA from DNA sample - (reply: 15)
2077. Only DNA ladder , No desired band in PCR - (reply: 4)
2078. taq and PCR - (reply: 6)
2079. Molar concentration of GTC in Ambions Tri Reagant? - Molar concentration of GTC in Ambions Tri Reagant? (reply: 1)
2080. is too much ligation reaction bad for transformation? - (reply: 4)
2081. question about restriction enzyme digest - (reply: 1)
2082. Does purifying PCR probes for EMSA from EtBr gel interfere with binding? - (reply: 1)
2083. RNA gel electrohoresis - (reply: 1)
2084. plasmid dna isolation - (reply: 1)
2085. Two stop codons - (reply: 1)
2086. About antibodies - How resistant are they (reply: 2)
2087. Vector needed - (reply: 1)
2088. Long PCR and genomic DNA isolation problems - (reply: 2)
2089. having the wrong vector in my clone - (reply: 3)
2090. Low Quality Seqeunces - (reply: 3)
2091. could FLAG-tagged protein be used in the Luc assay? - (reply: 1)
2092. Removal of Methionine in E.coli - (reply: 1)
2093. 20x SSC - northern transfer (reply: 3)
2094. Sequence direction same - (reply: 1)
2095. TN5 library - (reply: 4)
2096. Slow cell culture growth? - (reply: 3)
2097. cell lysis buffer - (reply: 1)
2098. Primer design: free energy - (reply: 2)
2099. Dot Blot Hybridization using DIG-labeled probes - Help needed! (reply: 6)
2100. stupid question on cloning - what part of cDNA is really needed? (reply: 2)