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If you decide to place an order during this period, we reserve the right to adjust the price based on the evolving situation. We understand that market changes may cause inconvenience. We will negotiate with you if there’s a significant price fluctuation due to tariff policy changes before the order’s actual delivery, and in such cases we may adjust or cancel the order as necessary.

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Key Documents

Safety Information

Z374911

PCR multiwell plates

size 384 wells, polypropylene, skirt, non-sterile

Synonym(s):

384 multiwell PCR plate, 384 well PCR microplate, 384 well PCR plate, 384 well microtiter plate

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1 PKG
¥3,920.91

¥3,920.91


Estimated to ship on2025年6月19日Details



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1 PKG
¥3,920.91

About This Item

UNSPSC Code:
41106300
NACRES:
NB.22

material:
colorless polypropylene
polypropylene
size:
384 wells
sterility:
non-sterile
non-sterile
feature:
skirt

¥3,920.91


Estimated to ship on2025年6月19日Details


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)

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General description

384 well PCR plates are skirted for compatibility with automation systems. Wells have raised rims to ensure contact with sealing film and reduce evaporation. Each well has a capacity of 40 μL and a working volume of 25 μL.
A rigid top plate (included) minimizes plate distortion, assures a dependable fit with the PCR thermal cycler, and allows for a leak-proof seal with micro-mats or cap strips. Each well has a maximum capacity of 200 μL.

Features and Benefits

  • Virgin polypropylene
  • Fully autoclavable
  • Certified DNase- and RNase-free
  • Wells have thin walls for rapid temperature equilibration and reduced cycle time

Regulatory Information

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Protocols

Reverse transcription (RT) is the process of converting RNA to cDNA using a reverse transcriptase enzyme and dNTPs.

Hot Start dNTPs block DNA polymerase until heat activation, enhancing PCR specificity.

Perform reverse transcription (RT) using a reverse transcriptase enzyme and dNTPs. Use total RNA or a gene-specific approach so that only the RNA of interest is converted to cDNA.

Method for amplification of DNA from damaged DNA sources. Particularly useful for DNA extracted from old samples.

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