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    Production and characterisation of monoclonal antibodies against immunoglobulins of Cirrhinus mrigala (Hamilton 1822)

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    Serum immunoglobulins (Ig) of mrigal Cirrhinus mrigala (Hamilton 1822) immunised with bovine serum albumin (BSA), were purified by affinity chromatography using BSA-CL agarose column. The purified mrigal Ig (m-Ig) was characterised under reducing condition by Sodium Dodecyl Sulphate Polyacrylamide Gel Electrophoresis (SDS-PAGE) which revealed two bands of 85 and 26 kDa corresponding to heavy and light chain, respectively. Following fusion of splenocytes from Balb/c mice immunised with purified m-Ig with myeloma cells, three hybridomas showing reactivity with m-Ig were cloned by limiting dilution. The monoclonal antibodies (MAbs) generated by these clones were designated as 3B2-E12, 3B2-F9 and 4C3-B2 and characterised by western blotting and isotyping. Western blot analysis of the supernatant from the three clones with purified m-Ig indicated that, all the three MAbs were specific to heavy chain. Isotyping revealed that 3B2-E12 MAb was of IgG1 isotype whereas the other two MAbs were of IgG2a isotype. Cross reactivity of anti-mrigal Ig MAb (3B2-E12) was observed with serum Ig of Catla catla and Labeo rohita indicating semi-conserved nature of Ig in Indian major carps

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    Not AvailableFingerling rearing of pengba, Osteobrama belangeri, was conducted at varied densi-ties for 90 days in 12 outdoor concrete tanks (10 m × 5 m × 1 m). The tanks, grouped into four triplicated treatments, were stocked with fry at 20, 30, 40 and 50 fry m-3; and designated as control, T-1, T-2 and T-3 respectively. Tanks were filled up to 90 cm depth. Evaporation loss compensated fortnightly. Fish sampling and monitoring of water quality parameters done at fortnight intervals. Survival varied between 71.5% and 84.0% in treatments. Both survival and total length significantly reduced with increasing densities from control to T-2 (p .05). Similarly, significant reductions in final body weight and specific growth rate were observed with increased densities and these values further reduced in T-3 than T-2 (p < .05). Such results corroborated the inverse relationship between stocking density and growth. Gross biomass yields in two higher densities (T-2 and T-3), despite their lower survivals, were significantly higher than the two lower densities. The numbers of fingerlings harvested were 35, 74 and 112% higher than the control in T-1, T-2 and T-3 respectively. The lowest size obtained even at the highest density (T-3) was of 7.0 ± 1.0 cm and 3.99 ± 0.17 g, which can be considered as ideal grow-out stocking size of pengba. Therefore, the study showed feasibility of stocking up to 50 fry m-3 for rearing from fry to fingerling stage. However, the other lower densities may be used in case of requirement of larger fingerlings.Not Availabl

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    Not AvailableSerum immunoglobulins (Ig) of mrigal Cirrhinus mrigala (Hamilton 1822) immunised with bovine serum albumin (BSA), were purifed by affnity chromatography using BSA-CL agarose column. The purifed mrigal Ig (m-Ig) was characterised under reducing condition by Sodium Dodecyl Sulphate Polyacrylamide Gel Electrophoresis (SDS-PAGE) which revealed two bands of 85 and 26 kDa corresponding to heavy and light chain, respectively. Following fusion of splenocytes from Balb/c mice immunised with purifed m-Ig with myeloma cells, three hybridomas showing reactivity with m-Ig were cloned by limiting dilution. The monoclonal antibodies (MAbs) generated by these clones were designated as 3B2-E12, 3B2-F9 and 4C3-B2 and characterised by western blotting and isotyping. Western blot analysis of the supernatant from the three clones with purifed m-Ig indicated that, all the three MAbs were specifc to heavy chain. Isotyping revealed that 3B2-E12 MAb was of IgG1 isotype whereas the other two MAbs were of IgG2a isotype. Cross reactivity of anti-mrigal Ig MAb (3B2-E12) was observed with serum Ig of Catla catla and Labeo rohita indicating semi-conserved nature of Ig in Indian major carps.Not Availabl
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