Chicken Of Cut
Mostrando 13-24 de 32 artigos, teses e dissertações.
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13. Effects of incorporating soy protein isolate and dried bovine plasma in features of a product restructured chicken / Efeitos da incorporação de isolado proteico de soja e plasma bovino desidratado nas caracteristicas de um produto reestruturado de frango
As técnicas de reestruturaçãode carne estão tendo uma grande importância no desenvolvimento da indústria avícola moderna. A elaboração de produtos reestruturados permite apyoveitar cortes ou carcaças de inferior valor comercial e, além disso, permite o emprego de derivados protéicos não cárneos, que podem contribuir para melhorar algumas qualid
Publicado em: 1985
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14. Avaliação sensorial e reologica de carne e aves : influencia da congelação e da suplementação alimentar com lecitina de soja sobre a textura
The aim of this work was to test the effect of the addition of soybean, lecithin to chicken feed and its influence on the texture of frozen and non-frozen meat (breast and thighs) At the same time, the investigation sought to establish comparison between two objective methods and two subjective methods of- texture evaluation and to correlate processes and me
Publicado em: 1976
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15. The presence of ovalbumin mRNA coding sequences in multiple restriction fragments of chicken DNA.
Chicken DNA has been digested with restriction enzymes and the size distribution of the DNA fragments containing ovalbumin specific sequences has been examined after separation of the fragments on agarose gels and transfer to nitrocellulose sheets. Hybridisation with terminally 32P-labelled ovalbumin mRNA fragments or with RNA populations transcribed from th
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16. Sites of integration of reticuloendotheliosis virus DNA in chicken DNA.
The pattern of integration of spleen necrosis virus (SNV) DNA in DNA from a large population of SNV-infected chicken cells was studied by nucleic acid hybridization with iodinated viral RNA by the blotting technique of Southern. SNV DNA was found to be integrated at multiple sites in acutely infected chicken cells. Concomitant with the transition from acute
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17. The ovalbumin gene: structural sequences in native chicken DNA are not contiguous.
The sequence organization of the structural ovalbumin gene and flanking sequences in native chicken DNA was studied by restriction mapping and filter hybridization using a nick-translated probe generated from pOV230, a recombinant plasmid that contains a full-length ovalbumin DNA synthesized from ovalbumin mRNA. The structural sequences of the ovalbumin gene
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18. Opposite replication polarities of transcribed and nontranscribed histone H5 genes.
We used an in vitro nuclear runoff replication assay to analyze the direction of replication of the active and inactive histone H5 genes in avian cells. In embryonic erythrocytes the transcribed histone H5 gene displayed sensitivity to endogenous nuclease cleavage. In contrast, this gene was insensitive to endogenous nuclease digestion under the same conditi
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19. Rapid Method for Detection and Enumeration of Fecal Coliforms in Fresh Chicken
A rapid method for enumerating fecal coliforms in foods was developed employing an agar pour-plate medium. After 7 h of incubation at 41.5 ± 0.05 C, this medium effectively allows the growth of fecal coliforms only. This rapid method was compared with the Association of Official Analytical Chemists multiple-tube dilution method for Escherichia coli, by usin
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20. Toxic effects of ochratoxin A and citrinin, alone and in combination, on chicken embryos.
The embryotoxic potential of ochratoxin A and citrinin was studied after administering, either subgerminally or intraamniotically, single mounting doses of the mycotoxins to chicken embryos on days 2, 3, and 4. The beginning of the embryotoxicity dose range was found to be between 0.01 to 0.05 microgram for ochratoxin A and 1 to 10 micrograms for citrinin. T
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21. Identification of Rickettsia rickettsii in formalin-fixed, paraffin-embedded tissues by immunofluorescence.
With slight modification of a trypsin digestion technique, Rickettsia rickettsii were demonstrated specifically by immunofluorescence staining in Formalin-fixed, paraffin-embedded tissue sections from a human, rhesus monkey, and guinea pig with Rocky Mountain spotted fever and in infected membranes from a chicken embryo. Tissues were cut at 4 micron and, usi
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22. Large-Quantity Production of Chicken Embryo Tracheal Organ Cultures and Use in Virus and Mycoplasma Studies
Chicken tracheal organ cultures were made from embryos which were 19 to 20 days old. Transversely cut rings of trachea were placed in screw-capped tissue-culture tubes with Eagle's-N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid (HEPES) medium and incubated in roller drums. The method had advantages over other organ culture systems in that these cultur
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23. Identification of clones that encode chicken tropomyosin by direct immunological screening of a cDNA expression library.
A cDNA library of approximately equal to 9,000 members has been prepared from chicken smooth muscle mRNA by using the plasmid expression vector pUC8. Addition of Sal I and EcoRI linkers at different stages during the preparation of the cDNA resulted in a population of molecules, most of which had EcoRI linkers at the end of the cDNA that corresponded to the
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24. Cooperative transformation studies with temperature-sensitive mutants of Rous sarcoma virus.
Stocks of Rous sarcoma virus Bryan strain were mutagenized using a bromodeoxyuridine treatment immediately after infection. Thirty temperature-sensitive (ts) mutants defective in transformation (td) were isolated by a replica plating technique. Twenty of these mutants were preliminarily characterized and found to be defective in late functions related to tra