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Cloning and expression analysis of apolipoprotein AI (ApoA-I) in the Hong Kong grouper (Epinephelus akaara)

Aquaculture. 2014; 
MengQuXiaohongHuangXiaojieZhangQiaohongLiuShaoxiongDing
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Catalog Antibody To confirm the expression of the 6’ His-tagged protein, we performed Western blotting analysis using standard techniques as described by Wang et al. (Wang et al., 2012). The recombinant protein was separated using 12% SDS-PAGE and then transferred to a PVDF membrane (Hybond-p; Amersham Pharmacia Biotech AB, Uppsala, Sweden) according to the manufacturer’s instructions. The monoclonal mouse anti-His-tag antibody (1:10000 dilution) was used as the primary antibody, while the HRP-labeled Goat Anti-Mouse IgG (GenScript, China) (1:1000 dilution) was used as the secondary antibody. The specific antigen-bound antibody was visualized with DAB (3,3?-Diaminobenzidine) reagent (Sigma, USA). Get A Quote

摘要

Apolipoprotein A-I (ApoA-I) is the principal protein component of plasma high-density lipoprotein (HDL). It plays an important role in lipid transport and uptake and has been demonstrated to defend against bacteria in vertebrates. In this report, we identified a cDNA sequence from?E. akaara?ApoA-I with an ORF of 792?bp encoding a putative polypeptide of 263 amino acid residues that shares some common features with known vertebrate ApoA-I sequences. Tissue distribution analysis indicated that ApoA-I mRNA is broadly expressed in all tissues tested, including the fat metabolic organs (liver and intestine). We successfully expressed the ApoA-I gene using a pET28a(+) vector and acquired a highly purified protein ... More

關鍵詞

Apolipoprotein A-IHigh density lipoproteinEpinephelus akaaraInnate immunityLipid metabolism
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