1999
DOI: 10.1016/s0924-2244(99)00013-8
|View full text |Cite
|
Sign up to set email alerts
|

Challenges in the identification of species of canned fish

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
84
0
6

Year Published

2001
2001
2017
2017

Publication Types

Select...
4
4

Relationship

0
8

Authors

Journals

citations
Cited by 141 publications
(91 citation statements)
references
References 12 publications
0
84
0
6
Order By: Relevance
“…Analytical methods are focused mainly on protein or DNA molecules, which are extracted from the fish tissues. Owing to the protein denaturation caused by heating or canning (high temperature in combination with high pressure) processes, [5] DNA is a more suitable molecular marker for fish species authentication because it is more resistant to thermal treatment. Indeed, DNA is also degraded into small fragments during the thermal process but these are still detectable.…”
Section: Introductionmentioning
confidence: 99%
“…Analytical methods are focused mainly on protein or DNA molecules, which are extracted from the fish tissues. Owing to the protein denaturation caused by heating or canning (high temperature in combination with high pressure) processes, [5] DNA is a more suitable molecular marker for fish species authentication because it is more resistant to thermal treatment. Indeed, DNA is also degraded into small fragments during the thermal process but these are still detectable.…”
Section: Introductionmentioning
confidence: 99%
“…Traditional and official methods used in species identification, including fish, are based chiefly on the separation and characterization of specific proteins using electrophoretic techniques, such as isoelectric focusing: IEF (Rehbein 1990) and capillary electrophoresis: CE (Kvasnička 2005), high performance liquid chromatography: HPLC (Hubalkova et al 2007), or immunoassay systems, such as EnzymeLinked ImmunoSorbent Assay: ELISA ) (for a complete review see e.g., Mackie et al 1999;Civera 2003; Moretti et al 2003;Hubalkova et al 2007). Nowadays, different companies commercialize ELISA diagnostic kits for various applications, such as the authentication of species in milk and cheese ).…”
Section: Introductionmentioning
confidence: 99%
“…Tahapan PCR terdiri dari predenaturasi 94˚C selama 5 menit, denaturasi 94 ukurannya lebih kecil, jumlah salinannya banyak, informasi urutan DNA tersedia lengkap untuk organisme akuatik, dan tidak ada rentang non-coding (Mackie et al 1999). DNA barcoding merupakan metode yang sering digunakan dalam forensik taksonomi karena efektif dalam mengidentifikasi dalam berbagai kondisi sampel uji dan tidak menghasilkan data yang ambigu (Dawnay et al 2007;Wong et al 2011).…”
Section: Amplifikasi Pcrunclassified