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CHF 446.00
CHF 446.00
Über diesen Artikel
polypropylene
non-sterile
Fortfahren mit
Produktname
PCR multiwell plates, size 384 wells, polypropylene, skirt, non-sterile
material
colorless polypropylene
polypropylene
sterility
non-sterile
non-sterile
feature
skirt
packaging
case of 50 ea
manufacturer/tradename
Sorenson 39620
technique(s)
PCR: suitable
size
384 wells
well volume
40 μL
well working volume
25 μL
suitability
suitable for (PCR, RT-PCR or DNA purification applications)
application(s)
agriculture
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1 of 4
Dieser Artikel | Z374903 | CLS3757 | CLS6511 |
|---|---|---|---|
| manufacturer/tradename Sorenson 39620 | manufacturer/tradename Sorenson 2633 | manufacturer/tradename Corning 3757 | manufacturer/tradename Corning 6511 |
| sterility non-sterile | sterility non-sterile | sterility non-sterile | sterility non-sterile |
| material colorless polypropylene | material colorless polypropylene , colorless wells | material clear bottom, clear polypropylene , conical bottom | material clear plate, clear polycarbonate plate, conical bottom clear wells |
| size 384 wells | size 96 well | size 384 wells | size 96 wells |
| suitability suitable for (PCR, RT-PCR or DNA purification applications) | suitability suitable for (PCR, RT-PCR or DNA purification applications) | suitability suitable for (high-throughput (HT) applications; PCR, DNA sequencing and RT-PCR) | suitability suitable for (PCR applications) |
| packaging case of 50 ea | packaging case of 25 ea | packaging pack of 10, case of 50 | packaging pack of 1, case of 25 |
Features and Benefits
- Virgin polypropylene
- Fully autoclavable
- Certified DNase- and RNase-free
- Wells have thin walls for rapid temperature equilibration and reduced cycle time
General description
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Protokolle
REDAccuTaq LA protocol offers high-fidelity amplification of long PCR fragments with direct gel loading capability.
JumpStart™ Taq DNA Polymerase is an antibody-inactivated, hot start enzyme.
Hot Start dNTPs block DNA polymerase until heat activation, enhancing PCR specificity.
Protocol using antibody mediated hot start polymerase. Method has short activation period (<1min), and results in higher yields and more specificity over standard PCR methods.
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