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Questions and Answers
What is the basic principle behind ELISpot?
What is the material used for most ELISA plates?
How many wells do 96-well ELISA plates typically have?
What is the volume each well of an ELISA plate can hold?
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Which type of plates are available for high throughput screening in ELISA?
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What is the main advantage of ELISA in terms of sensitivity?
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What is the purpose of Northern blotting?
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What is a disadvantage of the standard northern blot method?
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Which technique is used to analyze protein post translational modifications?
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What happens when RNA samples are degraded by RNAses in Northern blotting?
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Why does the use of radioactivity in Northern blotting pose a challenge?
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What is the main application of Northern blotting?
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Which technique is suitable for detecting carbohydrate epitopes?
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What is a drawback of using the standard northern blot method with multiple probes?
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Why is the standard northern blot method less sensitive than nuclease protection assays and RT-PCR?
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What happens if RNA samples are slightly degraded during northern blot analysis?
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