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CLS430909

Corning® microcentrifuge tubes with screw cap

1.5 mL microcentrifuge tube, polypropylene, w/ attached screw cap, w/ 0-ring, sterile, natural, 500/cs

Synonym(s):

centrifuge tubes, micrcentrifuge tubes, microfuge tubes, screw cap microcentrifuge tubes

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About This Item

UNSPSC Code:
41121703
eCl@ss:
32119210
NACRES:
NB.11

material

conical bottom tube
natural polypropylene tube
screw top cap

description

O-ring (black silicone, rubber O-ring in cap)

sterility

sterile

feature

self-standing: no conical bottom

packaging

pack of 50
case of 500

manufacturer/tradename

Corning 430909

parameter

20000 × g max. RCF

cap diam.

12.7 mm

capacity

1.5 mL

tube O.D.

10.7 mm

color

natural

fitting

cap (screw cap)

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General description

  • 1.5 mL polypropylene microcentrifuge tubes feature screw caps that provide a tight secure seal
  • Attached cap with silicone O-ring
  • Withstands a maximum RCF of 20,000xg
  • Sterile
Corning polypropylene microcentrifuge tubes feature screw caps that provide a tight, secure seal.
  • Maximum RCF is 20,000
  • No marking spot

Legal Information

Corning is a registered trademark of Corning, Inc.

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Protocols

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

The most common application for qPCR is the measurement of a gene transcript or copy number quantity relative to one or more reference genes using probe detection.

Hot Start dNTPs are modified with a thermolabile protecting group at the 3’ terminus. The presence of this modification blocks nucleotide incorporation by DNA polymerase until the nucleotide protecting group is removed during a heat activation step.

Reverse transcription is the analysis of gene expression to measure concentration mrna a gene. there are several challenges such analyses, as differences in halflife between different transcripts, temporal patterns and lack correlation protein.

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