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New Forum Archives (2009-)
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PCR--RT-PCR-and-Real-Time-PCR
271.
PCR product size confusion -
(reply: 3)
272.
Concentration specification in PCR -
(reply: 3)
273.
help us understand the run -
(reply: 1)
274.
Different MOI in comparison experiment -
(reply: 3)
275.
How to determine the size of gene to amplify? -
(reply: 1)
276.
Guanidine isothiocyanate in PCR -
(reply: 1)
277.
Untreated samples negative, how to analyze fold change? -
(reply: 1)
278.
Primers have worked well but now getting primer dimers? -
(reply: 2)
279.
I cannot design primers on exon-exon junction -
(reply: 2)
280.
DNA Quantification of PCR Products -
(reply: 2)
281.
In 2^ minus ddCt method, why is the "minus" sign? -
(reply: 1)
282.
Problem for PCR -
(reply: 9)
283.
Confused about my CT values -
(reply: 1)
284.
Designing primers in UTRs -
(reply: 1)
285.
Multiplex PCR -
(reply: 1)
286.
primer design@ buy? -
(reply: 2)
287.
High Ct/Cq values in my NO-RT and NTC samples -
(reply: 3)
288.
Dissolving DNA Oligos -
(reply: 2)
289.
Trouble with overlap extension pcr -
(reply: 3)
290.
copies per ul to copies per gram tissue -
(reply: 2)
291.
designing primers( selecting target sequence/amplicon design) -
(reply: 3)
292.
Question about the RT PCR -
(reply: 3)
293.
PCR ready mixes with long shelf lives -
(reply: 4)
294.
Problem with repeatability of the standard curve -
(reply: 3)
295.
Influenza virus -
(reply: 3)
296.
Defining standards in qPCR softwares -
(reply: 3)
297.
How to design primer to amplify genomic DNA? -
(reply: 3)
298.
Overlap PCR, need help -
(reply: 11)
299.
Internal control for miRNA RT-PCR -
(reply: 1)
300.
Primers -
(reply: 1)
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