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  • 1
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    In:  http://aquaticcommons.org/id/eprint/13062 | 9596 | 2014-02-19 21:18:40 | 13062 | Gulf and Caribbean Fisheries Institute
    Publication Date: 2021-07-08
    Description: File: POSTER SESSION ABSTRACTS GCFI:58 (2007). Information: Page range is taken from table of contents for Proceedings volume (page numbers in deposited article are incorrect due to publishing error).
    Keywords: Fisheries ; GCFI
    Repository Name: AquaDocs
    Type: conference_item
    Format: application/pdf
    Format: application/pdf
    Format: 493-494
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  • 2
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    In:  http://aquaticcommons.org/id/eprint/22803 | 18721 | 2018-05-23 20:58:41 | 22803 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-10
    Description: Streptococcus iniae is a major cause of serious bacterial infections in both fish and human beings. Capsular polysaccharide (CPS) of S. iniae is vital to evade phagocytic clearance of the host and serves as an important protective antigen of S. iniae infection in aquatic animals. The CpsD gene was determined to be highly conservative in capsule polysaccharide operon. Prokaryotic expression of the CpsD gene of a clinical isolate of S. iniae from channel catfish and immunogenic examination of the recombinant protein were first described in this essay. The recombinant protein was expressed in the form of inclusion bodies (IBs). Induction conditions in Escherichia coli were optimized with 0.6mM Isopropyl β-D-1-Thiogalactopyranoside at 37°C for 5h after the culture mid-log phase in Luria Bertani (LB) medium. The recombinant protein CpsD was thus expressed and purified by immobilized metal affinity chromatography (IMAC), yielding approximate 582.47 mg the protein per liter culture. Western blot analysis showed that the purified CpsD had reactogenicity. It will possibly reveal more details of capsule synthesis and capsule regulation during various stages of the S. iniae infectious process.
    Keywords: Aquaculture ; Biology ; Fisheries ; Streptococcus iniae ; Capsular polysaccharide ; Prokaryotic expression ; Purification ; Western blot analysis ; fish disease ; China ; immunogenicity
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 612-622
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  • 3
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    In:  http://aquaticcommons.org/id/eprint/22737 | 18721 | 2018-05-18 22:38:13 | 22737 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-09
    Description: Ayu (Plecoglossus altivelis), one kinds of valuable cultured fish species, show almost no morphological difference between male and female until sexual maturity. Here, we report the identification of sex-linked markers for the ayu, based on Amplified Fragment Length Polymorphism (AFLP) generated from cultured fish (15 males and 15 females) by using 63 different primer combinations. Genomic fragments (n = 3733) were produced with a mean frequency of 59 bands per primer pair. A male-specific of 139 base pair band was amplified and converted to a sequence-characterized amplified region (SCAR marker) designated as Ayu102. Six distinct genomic fragments were produced in 12 wild samples (6 males and 6 females). The fragments designated a, b, c, d, and e were detected only in males, and one fragment (f) was detected in both genders. Nucleotide sequence analysis showed that fragments e and f were 96.67% identical. Ayu102 marker was detected in 45-d-old larvae, in both cultured and wild fish populations, and in offsprings generated by gynogenesis. Fragment e was detected in all males, and in only 6.7% of females in cultured fish. Data suggest that Ayu102 marker is a male-specific marker linked to the sex-determining locus of the male ayu and can be used for gender identification.
    Keywords: Aquaculture ; Biology ; Fisheries ; AFLP ; Plecoglossus altivelis ; Sex-linked marker ; Biology ; Physiology ; China ; Identification ; population ; fish species ; sexual maturity
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 895-906
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