| bio | website | pigimal.com |
|---|---|---|
| location | Massachusetts | |
| age | 34 | |
| visits | member for | 11 months |
| seen | 15 mins ago | |
| stats | profile views | 9 |
Long-time OSS user/admin, beginning serious coder - I heart Python. Master of Science in Molecular Medicine, many years' experience in biotech working with antibodies and related assays. Science and computer geek. Dad.
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3h |
comment |
What mammalian cell lines are easiest to grow and transfect? good luck finding truly diploid cell lines - unless you're working with primary cells, most cell lines are transformed, and have all sorts of genetic anomalies. |
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14h |
reviewed | Reopen Specifically What Protein Folding Calculations does Folding@Home do? |
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1d |
reviewed | Approve suggested edit on Writing methods section on PCR amplication in a paper |
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1d |
comment |
How difficult is to renature a protein? @shigeta - I was specifically thinking of antibodies (150 kDa, 4 subunits disulfide-bonded to each other). At my previous job we experimented with purifying antibodies by eluting them from an antigen column with varying concentrations of guanidine, then dialyzing directly into PBS. We didn't do any biophysical characterization to look at the extent of denaturation, but in our functional assays they performed similarly to those eluted by the standard (pH-dependent) method. |
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May 17 |
revised |
How difficult is to renature a protein? edited tags |
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May 17 |
answered | How difficult is to renature a protein? |
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May 17 |
comment |
Writing methods section on PCR amplication in a paper Tag should probably be Taq... |
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May 17 |
reviewed | Close What molecules/elements/compounds are in the cardiovascular system? |
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May 17 |
comment |
Writing methods section on PCR amplication in a paper You should change your "Amplification..." sentence to remove the word "condition" and change 25 ml to 25 µL, but other than that it looks okay. Also, maybe spell out "Forward" and "Reverse" when listing your primers. |
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May 17 |
reviewed | Reviewed Primer design for Gibson assembly |
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May 17 |
revised |
Primer design for Gibson assembly formatting, link to Gibson assembly |
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May 16 |
comment |
What material is recommended for autoradiography cassettes when working with 32P? If you're worried, contact your local radiation safety committee - they should have a wide-spectrum detector around that can detect Bremsstrahlung. I've only ever used aluminum/plastic cassettes myself for autorads. The phosphor screen should block a good deal, but you do not want to take any chances where radiation is concerned... |
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May 14 |
revised |
Modularity of transcription factors added 446 characters in body |
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May 14 |
reviewed | Close Recent and good quality articles on systems biology |
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May 14 |
reviewed | Close Basic book on Human brain anatomy |
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May 13 |
answered | Breeding laboratory mice with cancer; how does this work? |
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May 13 |
revised |
SNPs mapping into protein deleted 2 characters in body; edited title |
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May 13 |
comment |
SNPs mapping into protein thank you for using one of my favorite gene names :) |
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May 13 |
comment |
SNPs mapping into protein I assume SNP means Single-Nucleotide Polymorphism? I'm confused exactly what your question is - how does one take a SNP and see what effect it has on the protein sequence? Is that it? |
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May 12 |
revised |
Is it possible to print humans? edited body; edited tags |
