tag:blogger.com,1999:blog-22337721272611161902012-02-16T12:23:46.653-08:00produksi dan penjualan batik pekalonganbiotechnologyhttp://www.blogger.com/profile/12498763748278941786noreply@blogger.comBlogger21100tag:blogger.com,1999:blog-2233772127261116190.post-14997875035656246882008-08-13T23:06:00.000-07:002008-08-13T23:10:34.792-07:00Tg Abs (normal range, <100> immunoradiometric assay kit (Biochem Immunosystem, Bologna,Italy) whereas TPO Abs (normal range, <10> by RIA kit set (DiaSorin, Inc., Saluggia, Italy). The detectionlimit of the assays, the intra- and interassay coefficientsof variation were: 5.0 U/ml, 3.9% and 6.9%, for Tg Ab and 0.7U/ml, 2.5% and 6.6%, for TPO Abs, respectively. Quality controlpools at low, normal, and high concentrations for all parameterswere present in each assay. Samples were assayed in duplicate.Serum IP-10/CXCL10 levels were assayed by a quantitative sandwichimmunoassay using a commercially available kit (R&amp;D Systems,Minneapolis, MN), with a sensitivity ranging from 0.41 and 4.46pg/ml and a mean minimum detectable dose of 1.67 pg/ml. Theintra- and interassay coefficients of variation were 3% and6.9%.<br />http://ajp.amjpathol.org/cgi/content/full/161/1/195<div class="blogger-post-footer"><img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/2233772127261116190-1499787503565624688?l=biotechnology-solution.blogspot.com' alt='' /></div>biotechnologyhttp://www.blogger.com/profile/12498763748278941786noreply@blogger.com0tag:blogger.com,1999:blog-2233772127261116190.post-88749010463989038072008-08-13T22:39:00.000-07:002008-08-13T23:00:32.664-07:00<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://1.bp.blogspot.com/_cf4IsUhh06I/SKPJzzLor2I/AAAAAAAAAAM/JpI07u_uwMY/s1600-h/jh0723221001.gif"><img style="margin: 0pt 10px 10px 0pt; float: left; cursor: pointer;" src="http://1.bp.blogspot.com/_cf4IsUhh06I/SKPJzzLor2I/AAAAAAAAAAM/JpI07u_uwMY/s320/jh0723221001.gif" alt="" id="BLOGGER_PHOTO_ID_5234249083684171618" border="0" /></a><br />IP-10/CXCL10 and Mig/CXCL9 expression in thyroid tissue specimens from patients with GD. <b>A:</b> Section of normal thyroid hybridized with anti-sense IP-10/CXCL10 mRNA probe showing virtually no signal. <b>B:</b> Section of a TA hybridized with anti-sense IP-10/CXCL10 mRNA probe showing virtually no signal. <b>C:</b> High signal in the thyroid specimen from a patient with GD hybridized with anti-sense IP-10/CXCL10 mRNA probe. <b>D:</b> Absence of signal in a consecutive section hybridized with a sense IP-10/CXCL10 mRNA probe. <b>E:</b> High-power magnification of the thyroid follicular epithelium from the same patient with GD hybridized with anti-sense IP-10/CXCL10 mRNA probe. <b>F:</b> Section of normal thyroid hybridized with anti-sense Mig/CXCL9 mRNA probe showing virtually no signal. <b>G:</b> Section of a TA hybridized with anti-sense Mig/CXCL9 mRNA probe showing virtually no signal. <b>H:</b> High signal in the thyroid specimen from a patient with GD hybridized with anti-sense Mig/CXCL9 mRNA probe. <b>I:</b> High-power magnification of the thyroid follicular epithelium from the same patient with GD hybridized with anti-sense Mig/CXCL9 mRNA probe. Dark-field original magnifications: <span style="font-family:ariel,helvetica;">x</span>100 (<b>A–D</b>, <b>F–H</b>); <span style="font-family:ariel,helvetica;">x</span>1000 (<b>E</b>, <b>I</b>).<br />http://ajp.amjpathol.org/cgi/content/full/161/1/195<div class="blogger-post-footer"><img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/2233772127261116190-8874901046398903807?l=biotechnology-solution.blogspot.com' alt='' /></div>biotechnologyhttp://www.blogger.com/profile/12498763748278941786noreply@blogger.com0