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PHCC20040

Millipore

Scepter 2.0 Handheld Automated Cell Counter

Rapid cell counts in a handheld easy to use format, includes pkg of 40 μm Scepter Cell Counter Sensors

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About This Item

Kod UNSPSC:
41104923
eCl@ss:
32011202
NACRES:
NB.22

producent / nazwa handlowa

Scepter

metody

cell counting: suitable

wielkość cząstki

3-18 μm

kompatybilność

for use with cells sized 4-12 μm

Warunki transportu

ambient

Opis ogólny

The Scepter 2.0 handheld automated cell counter provides a fast and convenient method for counting cells and particles and is compatible with both the 40 and 60uM sensor. The system employs the Coulter principle in a miniaturized, handheld, format enabling rapid cell counting; what used to take 10 minutes now takes less than 30 seconds. The user prepares a dilution of the cell culture of interest and uses the Scepter cell counter to aspirate a sample of this dilution into the Scepter sensor.

The Scepter cell counter’s screen displays:

Cell concentration
Average cell size
Average cell volume
Histogram of size or volume distribution
This system is intended for research use only and has been tested with cell types representative of those in use today.
The Scepter Cell Counter delivers rapid cell counts in a handheld easy to use format. Its on screen instructions guide you through the sampling process and in less than 40 seconds reveil data on cell concentration, average diameter, average volume and a histogram displaying population information on your culture. The device stores up to 72 counts which can be downloaded to your computer and uploaded to Excel for further manipulation.
FREE PACK OF 40μM Sensors included.

Zastosowanie

Research Category
Cell Culture

Komponenty

1 Scepter Cell Counter

1 Test Bead Vial

1 USB Cable

1 Downloadable Software

2 O-rings

50 Sensors (40µM)
This page may contain text that has been machine translated.

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Odwiedź Bibliotekę dokumentów

Zhiyin Xun et al.
Mechanisms of ageing and development, 133(4), 176-185 (2012-02-18)
Retinoic acid (RA) is used in differentiation therapy to treat a variety of cancers including neuroblastoma. The contributing factors for its therapeutic efficacy are poorly understood. However, mitochondria (MT) have been implicated as key effectors in RA-mediated differentiation process. Here
Reduction of infarct size by intravenous injection of uncultured adipose derived stromal cells in a rat model is dependent on the time point of application.
van Dijk, A, et al.
Stem Cell Research, 7, 219-229 (2011)
N H Foley et al.
Cell death and differentiation, 18(7), 1089-1098 (2011-01-08)
MicroRNAs function as negative regulators of posttranscriptional gene expression, having major roles in cellular differentiation. Several neuroblastoma cell lines can be induced to undergo differentiation by all-trans-retinoic acid (ATRA) and are used for modeling signaling pathways involved in this process.
Erin N Potts-Kant et al.
Free radical biology & medicine, 52(3), 705-715 (2011-12-27)
This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/our-business/policies/article-withdrawal). This article has been retracted at the request of the Authors. Since learning of potential discrepancies between the raw data from the animal pulmonary physiology
Oncogenes induce senescence with incomplete growth arrest and suppress the DNA damage response in immortalized cells.
Sherman, Michael Y, et al.
Aging Cell, 10, 949-961 (2011)
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Protokoły

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How to use Scepter™ 2.0 Cell Counter

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