Comparison of an image cytometry somatic cell count analyzer to a flow cytometry analyzer

نویسندگان

چکیده

The objective of this study was to evaluate the performance a small footprint benchtop somatic cell counter based on image cytometry (LactiCyte HD; Page and Pedersen International Ltd., Hopkinton, MA) against flow cytometer employed at regional dairy herd improvement (DHI) laboratory. Milk samples collected during monthly DHI testing were split into 2 samples. One sample evaluated using (Bentley SomaCount FCM; Bentley Instruments, Chaska, MN) laboratory, whereas other different levels (full number images, 16 pictures per slide; half 8 slide). Mean bias images −15,500 cells/mL, 21,800 cells/mL. When considering only counts ≤400,000 cells mL, for both imaging resolutions positive, meaning read higher than cytometer. Both (16 8) had concordance correlation coefficient greater 0.95. Considering ≥200,000 cells/mL be indicative subclinical mammary gland infection, sensitivity specificity 92.0% 91.7%, analyzer 85.7%, respectively. Method precision (repeatability; coefficients variation) calculated 3 (100,000, 200,000, 400,000 cells/mL) where each run repeatedly 12 times. analyzed full variation 16.9%, 11.7%, 10.9% 100,000, Analysis resulted in 18.9%, 24.8%, 8.7% We conclude that is an acceptable count on-farm use applications such as screening cows microbiological testing, superior when analysis performed allowed by instrument.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Comparison of DNA histograms by standard flow cytometry and image cytometry on sections in Barrett's adenocarcinoma

BACKGROUND The purpose of this study was to compare DNA histograms obtained by standard flow cytometry (FC) and high fidelity image cytometry on sections (ICS) in normal gastrointestinal mucosa and Barrett's adenocarcinoma (BAC). METHODS Archival formalin-fixed paraffin-embedded tissue blocks of 10 normal controls from 10 subjects and 42 BAC tissues from 17 patients were examined. DNA FC was ...

متن کامل

Flow Cytometry

Flow cytometry is a technology that has impacted both basic cell biology and clinical medicine in a very significant manner. The essential principle of flow cytometry is that single particles suspended within a stream of liquid are interrogated individually in a very short time as they pass through a light source focused at a very small region. The optical signals generated are mostly spectral ...

متن کامل

Flow Cytometry

Because it has been difficult to identify and separate malignant cells in human lymphoid malignancies, we have developed a flow cytometry-based fluorescent in situ hybridization (FISH) technique using immunoglobulin (Ig) heavy chain variable region (V H) gene probes. After obtaining the specific V H gene sequence expressed by the multiple myeloma IM-9 cell line and the malignant cells in five m...

متن کامل

Comparison of Flow Cytometry and Image-Based Screening for Cell Cycle Analysis

Quantitative cell state measurements can provide a wealth of information about mechanism of action of chemical compounds and gene functionality. Here we present a comparison of cell cycle disruption measurements from commonly used flow cytometry (generating onedimensional signal data) and bioimaging (producing two-dimensional image data). Our results show high correlation between the two approa...

متن کامل

Analysis of cell cycle by flow cytometry.

Described are four widely used procedures to analyze the cell cycle by flow cytometry. The first two are based on univariate analysis of cellular DNA content following cell staining with either propidium iodide (PI) or 4',6'-diamidino-2-phenylindole (DAPI) and deconvolution of the cellular DNA content frequency histograms. This approach reveals distribution of cells in three major phases of the...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: JDS communications

سال: 2023

ISSN: ['2666-9102']

DOI: https://doi.org/10.3168/jdsc.2023-0380