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1291. how can one get rid of genomic DNA in miniprep - (reply: 5)
1292. Get stuck in a subcoloning: put 0.6kb into 7kb - (reply: 8)
1293. Making blunt and stick end vector - (reply: 2)
1294. No colony after ligation - (reply: 6)
1295. Ligation worked - maybe? - Aimikins - I've got colonies! Which size do I pick? (reply: 4)
1296. Cloning a PCR product after digestion - (reply: 7)
1297. Which Klenow product to use?! - With or without exo-nuclease activity? (reply: 5)
1298. troobleshoting for colonies background - (reply: 3)
1299. Cloning of long gene - (reply: 1)
1300. Silly question concening REs - (reply: 6)
1301. Cutting close to DNA ends - (reply: 6)
1302. Problem in picking colonies after transformation - (reply: 9)
1303. basal expression - Is it possible in DH5a or in Rosetta pLYS? - (reply: 3)
1304. Distinguish uncut vs. cut plasmids on agarose gel - (reply: 9)
1305. toxic gene ligation/transformation URGENT HELP! - (reply: 1)
1306. why dephosphoration of vector is not recommended? - (reply: 3)
1307. Is OVER-dephosphorylation possible? - (reply: 2)
1308. Positive and negative controls for transformation - What controls to use (reply: 4)
1309. Reusing Qiagen Tips - (reply: 2)
1310. Problems in cloning shRNA - (reply: 13)
1311. problem in ligation and transformation - (reply: 18)
1312. dimers of dna (not primers) following digest or pcr? - (reply: 11)
1313. Ethanol precipitation problem - (reply: 7)
1314. What amount of insert:vector should I use if I want a 3:1 molar ratio? - (reply: 2)
1315. cloning restriction fragment for sequencing - (reply: 1)
1316. Prepping and transformation - (reply: 2)
1317. How do I check frame? - (reply: 3)
1318. Cloning with real time PCR fragments - using SyberGreen from Applied Biosystem (reply: 3)
1319. Many colonies but no positive clone - (reply: 1)
1320. converting overhang into blunt end - can i use Pfu instead Klenow? (reply: 3)
1292. Get stuck in a subcoloning: put 0.6kb into 7kb - (reply: 8)
1293. Making blunt and stick end vector - (reply: 2)
1294. No colony after ligation - (reply: 6)
1295. Ligation worked - maybe? - Aimikins - I've got colonies! Which size do I pick? (reply: 4)
1296. Cloning a PCR product after digestion - (reply: 7)
1297. Which Klenow product to use?! - With or without exo-nuclease activity? (reply: 5)
1298. troobleshoting for colonies background - (reply: 3)
1299. Cloning of long gene - (reply: 1)
1300. Silly question concening REs - (reply: 6)
1301. Cutting close to DNA ends - (reply: 6)
1302. Problem in picking colonies after transformation - (reply: 9)
1303. basal expression - Is it possible in DH5a or in Rosetta pLYS? - (reply: 3)
1304. Distinguish uncut vs. cut plasmids on agarose gel - (reply: 9)
1305. toxic gene ligation/transformation URGENT HELP! - (reply: 1)
1306. why dephosphoration of vector is not recommended? - (reply: 3)
1307. Is OVER-dephosphorylation possible? - (reply: 2)
1308. Positive and negative controls for transformation - What controls to use (reply: 4)
1309. Reusing Qiagen Tips - (reply: 2)
1310. Problems in cloning shRNA - (reply: 13)
1311. problem in ligation and transformation - (reply: 18)
1312. dimers of dna (not primers) following digest or pcr? - (reply: 11)
1313. Ethanol precipitation problem - (reply: 7)
1314. What amount of insert:vector should I use if I want a 3:1 molar ratio? - (reply: 2)
1315. cloning restriction fragment for sequencing - (reply: 1)
1316. Prepping and transformation - (reply: 2)
1317. How do I check frame? - (reply: 3)
1318. Cloning with real time PCR fragments - using SyberGreen from Applied Biosystem (reply: 3)
1319. Many colonies but no positive clone - (reply: 1)
1320. converting overhang into blunt end - can i use Pfu instead Klenow? (reply: 3)