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View:  Topic list, Topic summary Topics 1 - 10 of 46704  Older »
Description: Requests for information and lab reagents.
 

Why to use N-lauroylsarcosine for Hybridization? 
  Did you get an answer? I am asking the same question. In the protocols I have found, it has been used as a prehybridization step, along with formamide. The molecule is pretty big, I suspect it is used to sandwich itself between the two strands of a DNA or RNA, while the formamide deionizes the the bases, stabilizing dehybridization, prior to Probe-hybridization, but I am guessing.... more »
By michel saremi  - May 2 - 1 new of 1 message    

RNA/Protein UV crosslinking (UVXL) assay 
  Dear all, I am interested in an mRNA that has been described as being bound to the cytoskeleton. There are two published papers showing that a labelled fragment of the 3' UTR can be crosslinked to various (unidentified) proteins. I am hoping to identify the proteins and characterise them... more »
By Peter Ellis  - Apr 26 - 1 new of 1 message    

PEDOFILO FIGLIO DI PUTTANA PAOLO BARRAI (MERCATO LIBERO), CHE SI VANTA DI AVER SODOMIZZATO I FIGLI COSTANZA BARRAI E RICCARDO BARRAI, DA QUANDO IN CULLA (E GIA' QUESTO LA DICE TUTTA) IMBOSCAVA (E IMBOSCA) € DI LEGA LADRONA CON ARRESTATO BELSITO. 
  IN MOSTRUOSAMENTE CRIMINALE FINTER BANK LUGANO, CHIASSO, ZURICH E BAHAMAS, DI SCIACQUONE DI SOLDI MAFIOSI E, PARREBBE PURE SCIOCCANTEMENTE PEDOFILO GIOVANNI DEI CAS DA RANCATE IN NOVEZZANO ( [link] ), RICICLAVANO E RICICLANO OCEANI DI SOLDI ASSASSINI DI COSA NOSTRA, CAMORRA, NDRANGHETA, COME STRA RUBATI DA LL, LEGA LADRONA, E PDL, POPOLO DI LADRONI:... more »
By blogdiriferime...@gmail.com  - Apr 24 - 1 new of 1 message    

Plasmid mix in the clone - the mechanism? 
  DpnI digest? ...
By Vladimir Gainullin  - Apr 24 - 4 new of 4 messages    

5x sds sample buffer become brown color while preparing 
  Hello Everyone I was trying to prepare 5x sds sample buffer and it has become brown color instead of blue color. Could anyone please tell me what is the reason and please tell me your suggestions. The 5x sample buffer recipe 250mM tris-hcl ph 6.8(1M stock)------10ml 10% sds-------------------------4g r... more »
By Sudheer Sangeetham  - Apr 18 - 3 new of 3 messages    

How do I apply the genome scale reconstruction for E. coli in my experiments 
  Hi all, I have after a lot of struggle managed to develop a strain of E. coli that produces squalene. Now I want to find out genes that I can target to increase the synthesis of squalene. I have read a lot of papers on constrain based and dynamic models to find out these targets, but honestly... more »
By Yoginee Budhkar  - Apr 16 - 1 new of 1 message    

Any experiences with Geneamp 9700 cycler? 
  We've had the 9700 (over 10 years) for quite some time (over 10 years) with no real problems. Are you using the little black tube insert for single tubes and the red one for strip tubes? Without those you will crush the tubes (but I think these are similar to what gets used with the 2700 (which we also have). I will admit that I haven't watched the temps closely for quite some time, but we're not having problems with our PCR either.... more »
By Michael Sullivan  - Apr 16 - 5 new of 5 messages    

RNA isolation from Formaldehyde fixed samples 
  Dear All, I have some cells fixed in 4% formalin (neutral I believe). I was wondering if anyone has tried any RNA extraction on such cell/tissue samples, and if you have any wisdom including kits, tricks, solutions, problems that you'd share with me. I would appreciate it hugely. Thank you much,... more »
By Pow Joshi  - Apr 15 - 11 new of 11 messages    

Retroviral vector packaging compatibility 
  I have a lentiviral system working in my lab (pInducer), my PI wants to know if we could use a pBabe based vector as well. pBabe apparently has MMLV based LTR instead of HIV. My question is whether the packaging constructs I have for lentiviruses will work for MMLV? I'm guessing that HIV and MMLV have different capsids, which would... more »
By Ed Siefker  - Apr 15 - 1 new of 1 message    

protein estimation 
  Hello all I would like to quantify the protein concentration. I checked the nanodrop manual in that they have given that I can estimate the protein by measuring directly at 280 nm by giving extinction coefficient value without doing bradford or lowry methods. I would like to choose measuring the protein... more »
By Sudheer Sangeetham  - Apr 8 - 5 new of 5 messages    

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