A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer (
Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer...
Ausführliche Beschreibung
Autor*in: |
Liu, Guoqiang [verfasserIn] Luo, Jianxing [verfasserIn] Xu, Weiliang [verfasserIn] Li, Chundong [verfasserIn] Guo, Liang [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Journal of food composition and analysis - Orlando, Fla. : Academic Press, 1987, 121 |
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Übergeordnetes Werk: |
volume:121 |
DOI / URN: |
10.1016/j.jfca.2023.105390 |
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Katalog-ID: |
ELV010315128 |
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245 | 1 | 0 | |a A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( |
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520 | |a Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. | ||
650 | 4 | |a Triplex real-time PCR | |
650 | 4 | |a Sika deer | |
650 | 4 | |a Red deer | |
650 | 4 | |a Antlers | |
650 | 4 | |a Meat | |
650 | 4 | |a Authentication | |
700 | 1 | |a Luo, Jianxing |e verfasserin |4 aut | |
700 | 1 | |a Xu, Weiliang |e verfasserin |4 aut | |
700 | 1 | |a Li, Chundong |e verfasserin |4 aut | |
700 | 1 | |a Guo, Liang |e verfasserin |4 aut | |
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allfields |
10.1016/j.jfca.2023.105390 doi (DE-627)ELV010315128 (ELSEVIER)S0889-1575(23)00264-8 DE-627 ger DE-627 rda eng 630 640 540 660 VZ 58.34 bkl Liu, Guoqiang verfasserin aut A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. Triplex real-time PCR Sika deer Red deer Antlers Meat Authentication Luo, Jianxing verfasserin aut Xu, Weiliang verfasserin aut Li, Chundong verfasserin aut Guo, Liang verfasserin aut Enthalten in Journal of food composition and analysis Orlando, Fla. : Academic Press, 1987 121 Online-Ressource (DE-627)267328400 (DE-600)1469801-8 (DE-576)259483710 0889-1575 nnns volume:121 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.34 Lebensmitteltechnologie VZ AR 121 |
spelling |
10.1016/j.jfca.2023.105390 doi (DE-627)ELV010315128 (ELSEVIER)S0889-1575(23)00264-8 DE-627 ger DE-627 rda eng 630 640 540 660 VZ 58.34 bkl Liu, Guoqiang verfasserin aut A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. Triplex real-time PCR Sika deer Red deer Antlers Meat Authentication Luo, Jianxing verfasserin aut Xu, Weiliang verfasserin aut Li, Chundong verfasserin aut Guo, Liang verfasserin aut Enthalten in Journal of food composition and analysis Orlando, Fla. : Academic Press, 1987 121 Online-Ressource (DE-627)267328400 (DE-600)1469801-8 (DE-576)259483710 0889-1575 nnns volume:121 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.34 Lebensmitteltechnologie VZ AR 121 |
allfields_unstemmed |
10.1016/j.jfca.2023.105390 doi (DE-627)ELV010315128 (ELSEVIER)S0889-1575(23)00264-8 DE-627 ger DE-627 rda eng 630 640 540 660 VZ 58.34 bkl Liu, Guoqiang verfasserin aut A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. Triplex real-time PCR Sika deer Red deer Antlers Meat Authentication Luo, Jianxing verfasserin aut Xu, Weiliang verfasserin aut Li, Chundong verfasserin aut Guo, Liang verfasserin aut Enthalten in Journal of food composition and analysis Orlando, Fla. : Academic Press, 1987 121 Online-Ressource (DE-627)267328400 (DE-600)1469801-8 (DE-576)259483710 0889-1575 nnns volume:121 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.34 Lebensmitteltechnologie VZ AR 121 |
allfieldsGer |
10.1016/j.jfca.2023.105390 doi (DE-627)ELV010315128 (ELSEVIER)S0889-1575(23)00264-8 DE-627 ger DE-627 rda eng 630 640 540 660 VZ 58.34 bkl Liu, Guoqiang verfasserin aut A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. Triplex real-time PCR Sika deer Red deer Antlers Meat Authentication Luo, Jianxing verfasserin aut Xu, Weiliang verfasserin aut Li, Chundong verfasserin aut Guo, Liang verfasserin aut Enthalten in Journal of food composition and analysis Orlando, Fla. : Academic Press, 1987 121 Online-Ressource (DE-627)267328400 (DE-600)1469801-8 (DE-576)259483710 0889-1575 nnns volume:121 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.34 Lebensmitteltechnologie VZ AR 121 |
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10.1016/j.jfca.2023.105390 doi (DE-627)ELV010315128 (ELSEVIER)S0889-1575(23)00264-8 DE-627 ger DE-627 rda eng 630 640 540 660 VZ 58.34 bkl Liu, Guoqiang verfasserin aut A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. Triplex real-time PCR Sika deer Red deer Antlers Meat Authentication Luo, Jianxing verfasserin aut Xu, Weiliang verfasserin aut Li, Chundong verfasserin aut Guo, Liang verfasserin aut Enthalten in Journal of food composition and analysis Orlando, Fla. : Academic Press, 1987 121 Online-Ressource (DE-627)267328400 (DE-600)1469801-8 (DE-576)259483710 0889-1575 nnns volume:121 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.34 Lebensmitteltechnologie VZ AR 121 |
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Liu, Guoqiang @@aut@@ Luo, Jianxing @@aut@@ Xu, Weiliang @@aut@@ Li, Chundong @@aut@@ Guo, Liang @@aut@@ |
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630 640 540 660 VZ 58.34 bkl A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( Triplex real-time PCR Sika deer Red deer Antlers Meat Authentication |
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A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( |
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A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( |
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Liu, Guoqiang |
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Journal of food composition and analysis |
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Liu, Guoqiang Luo, Jianxing Xu, Weiliang Li, Chundong Guo, Liang |
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a novel triplex real-time pcr method for the simultaneous authentication of meats and antlers from sika deer ( |
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A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( |
abstract |
Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. |
abstractGer |
Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. |
abstract_unstemmed |
Deer products have been used as a traditional Chinese medical and edible food for over 2000 years. Due to the high price, the meats and antlers are often adulterated with low-value materials. The present study developed a triplex real-time PCR assay to simultaneously identify the DNA from sika deer and red deer in deer products. The triplex real-time PCR approach showed high specificity for 10 animal species, and the method simultaneously amplified an endogenous control to eliminate false-negative results. The absolute limits of detection for raw meat, meat product, and antlers were 0.00005–0.000025 ng, 0.00005–0.000025 ng, and 0.0001–0.000025 ng, respectively, for sika deer and 0.00005–0.000025 ng, 0.0005–0.00025 ng, and 0.0025–0.00025 ng, respectively, for red deer. This approach could determine 0.1% (w/w) adulteration. In conclusion, the established triplex real-time PCR assay displayed high specificity and sensitivity, and applicability and can be used for authentic animal products from sika deer and red deer.Data Availability: Data will be made available on request. |
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A novel triplex real-time PCR method for the simultaneous authentication of meats and antlers from sika deer ( |
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