| Thread | Last Post | Replies |
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| Looking for Bacterial phenotype database | 31 Aug 2006 18:37 GMT | 1 |
Hi, I am looking for the same kind of database. did you find any? Thanks Anis
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| Help with growth Trichoderma reesei ATCC 26921 | 29 Aug 2006 13:08 GMT | 1 |
I am a graduate student, I plan to grow Trichoderma reesei (ATCC 26921) and clone a gene inside it. I could buy this srain from ATCC, however, I couldn't access to the old publications describing how to grow it well and RNA extraction.
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| science project | 25 Aug 2006 21:34 GMT | 2 |
My son is doing a science project. we will be taking swabs of certain surfaces to see what is growing on them. what shoud we use and where can we buy these materials. help !
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| Camp test form primery culture | 20 Aug 2006 21:52 GMT | 1 |
Hai, does anyone know how to make crude Staphylococcal beta toxin, for identification of Streptococcus agalactiae from primery culture, is there any other effective method for identification for Streptococcus agalactiae beside Camp test and Lancefield's serrogrouping test
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| Do we have a moderator? | 20 Aug 2006 18:13 GMT | 14 |
If not, can we get one? There has to be some way of moderating what is posted on this board. --Alex
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| Energy vs. "Building Block" Requirements in Prokaryots and Eukaryots | 19 Aug 2006 18:16 GMT | 8 |
I was recently surprised to find out that in aerobic conditions + glucose medium E. Coli almost doesn't rely on the TCA cycle to produce energy i.e. all of the energy is produced from glycolysis (+respiration used the NADH glycolysis produces I guess), at least it is so in the
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| enumeration of non-cultureable bacteria | 19 Aug 2006 14:44 GMT | 6 |
Does anybody know how we can enumerate non-cultureable but viable bacteria (E.Coli) in the sea water to check environmental contamination? your answer will be really useful for me and I appreciate it. Reza
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| Penicillin: A Paradigm for Biotechnology | 17 Aug 2006 18:36 GMT | 5 |
Penicillin: A Paradigm for Biotechnology Richard I. Mateles, Editor Reprints The History of Penicillin Production, the classic publication of
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| methylene blue milk | 15 Aug 2006 04:14 GMT | 7 |
hai i just want to know what's the formula for making methylene blue milk for detecting Streptococcus Group D and how to determine positive and negative reaction thanks ---------------------------------
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| Need direction to study | 14 Aug 2006 08:26 GMT | 2 |
Hi people. I hope I can get a few sources where I can understand the factor that determine the host range of a viral infection. I know the factors are : - susceptibility
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| Microbial loading and enumeration | 11 Aug 2006 04:09 GMT | 1 |
What is microbial loading? When and where should it be done? Why is it that one has to choose plates that contain only 30 - 300 colonies? I'm doing an experiment that uses samples from the lake and pond and culturing the microorganisms in it using the streak and pour plate
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| how to get a rough idea how many bacteria are in the yoghurt? | 10 Aug 2006 11:54 GMT | 23 |
I want to count Lactobacilli in selfmade yoghurt. Should be easy, cheap and give an accuracy of about half a decade (favtor 3 uncertainity). Can I just homogenize a sample of the yoghurt, add DAPI, incubate it 15
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| Questions about cheese and foot odor and chemicals | 09 Aug 2006 22:42 GMT | 21 |
What chemicals other than diacetyl, butryic acid, isobutryic acid, propionic acid, valeric acid, and isovaleric acid are responsible for the cheesy foot odor? I am confused about methane thiol it MAYbe also resposible for foot
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| Renaturation of proteins on Ni-NTA column | 08 Aug 2006 20:49 GMT | 1 |
Has anybody tried to renature proteins bound to Ni-NTA (nickel-agarose) column? I use Qiagen protocol (washing the resign by linear gradent of urea in pH=8,0 buffer from 6M to 0,75M). However protein is not folded (CD,HPLC) moreover it dissapeared stored in 20% glycerol buffer (used
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| writing a paper with an aim to publish | 08 Aug 2006 20:46 GMT | 10 |
A long long time ago the forefront of science used to be in the garden sheds of eccentric victorian upper class and thus it was relatively easy to make discoveries worth writing about and worth publishing. These days its so much harder, most stuff that can be done in a shed
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