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dc.contributor.authorHuang, Z. P.zh_CN
dc.contributor.authorWang, J.zh_CN
dc.contributor.authorYu, H.zh_CN
dc.contributor.authorShen, W. X.zh_CN
dc.contributor.authorHuang, P.zh_CN
dc.contributor.authorTso, J. K.zh_CN
dc.contributor.authorYang, Z. M.zh_CN
dc.contributor.authorShen, Q. X.zh_CN
dc.contributor.author杨增明zh_CN
dc.date.accessioned2013-12-12T02:24:07Z
dc.date.available2013-12-12T02:24:07Z
dc.date.issued2003zh_CN
dc.identifier.citationActa Biochimica Et Biophysica Sinica,35(7):649-654zh_CN
dc.identifier.issn1672-9145zh_CN
dc.identifier.otherISI:000184466500010zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/65178
dc.description.abstractA cDNA encoding mouse implantation serine proteinase 2 (ISP2) was amplified from total cDNAs of mouse uterus implantation sites on D4. 5 of pregnancy by PCR, and sequenced ( GenBank accession No. A442918). DNA sequencing indicated that the ISP2 cDNA had an unreported 204 bp sequence at 3' untranslated region besides the open reading frame encoding 279 amino acid residues, which was identical with literature. In order to obtain recombinant ISP2 ( rISP2), an expression plasmid pGEX-4T-2/ISP2 was constructed and transformed into E. coli BL21 (DE3) strain. Expressed fusion protein GST-ISP2 was purified by SDS-PAGE and digested with thrombin, and the digestion mixture was subjected to SDS-PAGE again to recover rISP2. Rabbits were immunized using rISP2 as immunogen, and the polyclonal anti-ISP2 antisera Were obtained. Immunohistochemical analysis using this antisera showed, specific and high expression of ISP2 in mouse endometrial. gland epithelium in early pregnancy.zh_CN
dc.language.isoen_USzh_CN
dc.subjectISP2zh_CN
dc.subjectPCRzh_CN
dc.subjectgene expressionzh_CN
dc.subjectantibody preparationzh_CN
dc.titleCloning, expression, and antibody production of mouse ISP2zh_CN
dc.typeArticlezh_CN


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