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To design an effective in situ hybridization probe for accurate and specific detection of target sequences, one should consider the following steps:

  1. Select a target sequence that is unique to the gene of interest.
  2. Design a probe that is complementary to the target sequence and is of appropriate length (usually around 20-30 base pairs).
  3. Avoid regions of high sequence similarity with other genes to prevent non-specific binding.
  4. Consider the melting temperature (Tm) of the probe to ensure optimal hybridization conditions.
  5. Label the probe with a detectable marker, such as a fluorescent dye or enzyme, for visualization.
  6. Test the probe for specificity and sensitivity using control samples before conducting the in situ hybridization experiment.
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5mo ago

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