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Cellometer auto x4 cell counter

Manufactured by Revvity
Sourced in United States

The Cellometer Auto X4 Cell Counter is a compact and automated device designed for accurate cell counting. It utilizes advanced imaging technology to rapidly enumerate cells in liquid samples, providing reliable cell counts and viability assessment.

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6 protocols using cellometer auto x4 cell counter

1

Proliferation Assay for siRNA Knockdown

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To assess the proliferation rate, cells were seeded onto 6-cm plates (1 × 104 cells/well) and, after 24 h, were transfected with siRNA against OR5H2 or NT for 72 h (USPC1) or 48 h (USPC2) in triplicates. Cells were counted using a Cellometer Auto X4 Cell Counter (Nexcelom Bioscience, Lawrence, MA, USA) before and after transfection.
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2

Growth Analysis of Microalgae under Stress

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WT and NsAtWRI1 were cultivated under normal, N limitation, and osmotic stress conditions. Cell growth was analyzed by measuring cell density, specific growth rate, and dry cell weight (DCW). Cell density was estimated by the Cellometer Auto X4 Cell Counter (Nexcelom Bioscience, USA). Specific growth rate was calculated from cell density using the equation: Specific growth rate(μ/day)=ln(X2/X1)/(t2-t1), where X1 and X2 are the initial and final cell concentrations and t1 and t2 are the first and last days of culture. To determine DCW, cells were filtered with GF/C filter paper (Whatman, USA), washed with deionized water and dried at 105 °C overnight, after which cell weight was measured.
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3

Cell Proliferation Assay with siRNA

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To assess the proliferation rate, cells were seeded onto 6-cm plates (5 × 104 cells/well) and, after 24 h, were transfected with siRNA against UGT2B15, or NT, for 72 h (MCF7) or 96 h (T47D) in triplicates. Cells were counted using a Cellometer Auto X4 Cell Counter (Nexcelom Bioscience, Lawrence, MA, USA) before and after transfection.
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4

Measuring Dry Cell Weight and Growth Rate of N. gaditana

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The cell density of N. gaditana was determined using a Cellometer Auto X4 Cell Counter (Nexcelom Bioscience, USA). Samples were injected into a cell counting chamber with 20 μL volume each and measured in duplicate.
For measurement of the dry cell weight, cellulose nitrate membrane filters with a 0.45 μm pore size (Whatman, USA) were pre-dried in an oven at 80 °C. Suspensions of N. gaditana were passed through the filters using a vacuum pump, and then the filters were dried at 80 °C overnight. The dry cell weight was determined as follows: Dry cell weight=weight after filtration-(weight before filtration)volume of filtration Specific growth rate (μ) was calculated as follows: μ=lnX2-lnX1t2-t1 where t is time and Xi is the dry cell weight of N. gaditana at time ti.
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5

Algae Cell Concentration Quantification

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Algae cell concentrations were calculated by pipetting a 20 μL sample of each culture onto a Cellometer counting chamber (Nexcelom Bioscience, Lawrence, MA, USA) and analyzed using a Cellometer Auto X4 Cell Counter (Nexcelom Bioscience, Lawrence, MA, USA).
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6

Cell Growth and Metabolite Analysis

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Cell growth was determined by the cell density and dry cell weight (DCW). Cell density was measured using a Cellometer Auto X4 Cell Counter (Nexcelom Bioscience, USA). The DCW was determined by filtering the cells through a GF/C filter paper (47 mm; Whatman, UK), washing the filters with deionized water, drying them overnight at 105°C, and weighing them on a fine scale.
The concentration of nitrate (NO3-) in the medium was determined by an ion chromatograph (881 Compact IC Pro; Switzerland) with a Metrosep A Supp5 150 column for anions. The concentration of glucose was determined by a high-performance liquid chromatograph (Dionex Ultimate 3000; ThermoFisher Scientific) with an Aminex HPX-87H column.
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