Ear tissues from the end of the right ear were collected and stored in 75% alcohol for DNA extraction. Samples of the LD, SOL, psoas major (PM), masseter (MA), and biceps femoris (BF) muscles were collected for RNA extraction from four randomly selected healthy Suhuai pigs with similar body weight and age. LD muscle samples from the last rib of the carcass were collected and used to determine meat color. In China, traditional hot fresh meat is usually marketed immediately after slaughter, whereas chilled fresh meat is often cooled quickly to a stable 0–4°C within 24 h postmortem and maintained at this temperature until sold to the consumer (21 (link)). Therefore, meat color (L*a*and b*) was measured on the last rib at 2 (room temperature) and 24 h (4°C) postmortem using a chromameter (Minolta Camera Co., Osaka, Japan).
Chroma meter
The Chroma Meter is a compact, portable device designed for measuring and analyzing color parameters. It accurately captures color data, providing precise measurements of various color attributes such as chromaticity, luminance, and color temperature. The Chroma Meter is a versatile tool for applications that require accurate color evaluation and analysis.
Lab products found in correlation
39 protocols using chroma meter
Suhuai Pig Meat Color Analysis
Ear tissues from the end of the right ear were collected and stored in 75% alcohol for DNA extraction. Samples of the LD, SOL, psoas major (PM), masseter (MA), and biceps femoris (BF) muscles were collected for RNA extraction from four randomly selected healthy Suhuai pigs with similar body weight and age. LD muscle samples from the last rib of the carcass were collected and used to determine meat color. In China, traditional hot fresh meat is usually marketed immediately after slaughter, whereas chilled fresh meat is often cooled quickly to a stable 0–4°C within 24 h postmortem and maintained at this temperature until sold to the consumer (21 (link)). Therefore, meat color (L*a*and b*) was measured on the last rib at 2 (room temperature) and 24 h (4°C) postmortem using a chromameter (Minolta Camera Co., Osaka, Japan).
Pericarp Penetration Testing of Tomato Fruit
Example 6
Pericarp Penetration Test (PPT)
Phenotypic analysis was carried out on the S.pennellii ILs grown under glasshouse conditions in the UK. A 6 mm transverse section was cut from each fruit and the maximum load (force required to penetrate the pericarp tissue at 10 mm/minute) was measured using a Lloyd Instrument LRF+ machine (Lloyd, UK) equipped with a 10 N load cell and 1.6 mm probe. Measurements were taken separately from the outer and inner pericarp in duplicate. Fruit weight, truss position and colour were also recorded. Colour was measured using a Chroma Meter (Minolta).
Evaluating Meat Color Attributes
Ham Surface Color Measurement
Precise Color Measurement Technique
Color Analysis of Spent Hen Meat Patties
Comprehensive Analysis of Fruit Physico-Chemical Properties
Lycopene was extracted with reference to Salvia-Trujillo and McClements (Salvia-Trujillo and McClements, 2016 (link)), total phenolic compounds were extracted with reference to Toor and Savage (Toor and Savage, 2005 (link)), and total flavonoids according to Jia et al. (Jia et al., 1999 (link)), while carotenoids were extracted by the acetone method and then all were determined spectrophotometrically. The contents of pectin, vitamin C, soluble protein, soluble sugar and acidity were also determined by spectrophotometrically.
Evaluating Chicken Breast Meat Quality
Evaluating Tea Color Characteristics
Evaluating pH and Color of Ham with Essential Oils
The color of the ham samples was evaluated by taking at least five random readings from the surface of the different samples using a Minolta Chroma Meter fitted with CR-300 measuring head (Minolta, Osaka, Japan). Measurements of the instrument were standardized with respect to a white calibration plate, every time before use. The CIE (Commission Internationale de l’Eclairage), L*, a*, b*, colorimetry system was used for color determination with L* representing lightness, a* representing redness and b* representing yellowness. All of the measurements were collected from areas on the ham surface without visual excess fat, and the values were recorded for C* (chroma) calculation using the following equation: C* = (a*2 + b*2)1/2. Values regarding control and OEOF samples (without essential oil), were common with those reported in our previous paper [52 (link)], while the results relevant to the essential oil supplemented films—OEOS (which is the purpose of this paper) are reported for first time in the current paper.
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