Null hypothesis is either rejected or not rejected based on the viability of the given population or sample.

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#Id: 2743

#Unit 13. Methods in Biology

Polymorphism is produced due to the complementary sequence for the primer used being

present in one strain (strain A) but not in the other (strain B). As a result, an amplification product will be detectable as a band in strain A, while strain B will not show the product.

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#Id: 2744

#Unit 13. Methods in Biology

RAPDs behave as dominant markers and are recognized by the primer used for amplification.

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#Id: 2745

#Unit 13. Methods in Biology

RAPD bands are treated as independent loci;

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#Id: 2746

#Unit 13. Methods in Biology

A comparison between RFLP and RAPD markers for genome mapping in plan

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#Id: 2747

#Unit 13. Methods in Biology

RAPDs (Random amplified polymorphic DNAs) are obtained by using a PCR (polymerase chain reaction) equipment or a thermal cycler. 

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#Id: 2748

#Unit 13. Methods in Biology

The RAPD technique is based on PCR, which uses a DNA polymerase that is resistant to the high temperature needed for DNA denaturation; this permits the enzyme to be used repeatedly during the amplification process.