PCR Skirted Half Skirted Transparent plate
The technique is an enzymatic synthesis reaction relying on DNA polymerase in the presence of template DNA, primers and four deoxyribonucleotides. DNA polymerase initiates synthesis with the help of a small segment of double-stranded DNA as a template, forming a partial double strand by the binding of one or two synthetic oligonucleotide primers to a complementary sequence in the single-stranded DNA template. Under the right temperature and environment, DNA polymerase adds the deoxy mononucleotide to the 3´-OH end of the primer and, using this as a starting point, extends it along the 5´→3´ direction of the template to synthesise a new complementary strand of DNA.
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| 0.1ml 96 well clear PCR plate without skirt | | | |
| 0.2ml 96-well clear PCR plate without skirt | | | |
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| 0.1ml 96 well semi-skirted transparent PCR plate | | | |
| 0.2ml 96-well semi-skirted transparent PCR plate | | | |
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| 0.1ml 96 well Fully skirted transparent PCR plate | | | |
| 0.2ml 96-well Fully skirted transparent PCR plate | | | |
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| 0.1ml 96 well Fully skirted white PCR plate | | | |
| 0.2ml 96-well Fully skirted white PCR plate | | | |
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| 50ul 384 well fully skirted transparent PCR plate | | | |