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<script type=text/javascript> $(function(){ $("#ceshi").jqueryzoom({ xzoom:440, yzoom:440, offset:10, position:"right", preload:1, lens:1 }); /*$("#spec-list").jdMarquee({ deriction:"left", step:1, speed:4, delay:10, control:true, _front:"#spec-right", _back:"#spec-left" });*/ $("#spec-list li").bind("mouseover",function(){ var src=$(this).children().children('img').attr("src"); $("#ceshi").css("width", "100%"); $("#ceshi").css("height", "100%"); $("#ceshi").css("position", ""); $("#spec-n1 img").eq(0).attr({ src:src.replace("\/n5\/","\/n1\/"), jqimg:src.replace("\/n5\/","\/n0\/") }); $("#spec-list li p").each(function(){ $(this).css({ "border":"1px solid #ccc" }); }) $(this).children('p').css({ "border":"1px solid #244ca3" }); }); }) </script> <script type=text/javascript src="/Skins/270236/js/lib.js"></script> <script type=text/javascript src="/Skins/270236/js/zzsc.js"></script> </div> <div id="x4vfcpe" class="pro_detail_text"> <h1>SNP檢測 Taqman/MGB探針法</h1> <div id="x4vfcpe" class="jyms"><p><span>簡要描述：</span>SNP（single nucleotide polymorphism），即單核苷酸多態(tài)，是由于單個核苷酸改變而導(dǎo)致的核酸序列多態(tài)。一般來說，SNP在人基因組中的發(fā)生頻率比較高，大約平均每1000個堿基中就有一個多態(tài)位點，是繼微衛(wèi)星之后的第三代遺傳標(biāo)記。SNP廣泛用于群體遺傳學(xué)研究（如生物的起源、進(jìn)化及遷移等方面）和疾病相關(guān)基因的研究，在藥物基因?qū)W、診斷學(xué)和生物醫(yī)學(xué)研究中起重要作用。</p></div> <ul> <li><img src="/Skins/270236/images/dot.png" /><span>產(chǎn)品型號：</span></li> <li><img src="/Skins/270236/images/dot.png" /><span>廠商性質(zhì)：</span>生產(chǎn)廠家</li> <li><img src="/Skins/270236/images/dot.png" /><span>更新時間：</span>2024-05-13</li> <li><img src="/Skins/270236/images/dot.png" /><span>訪問量：</span>10994</li> </ul> <div id="x4vfcpe" class="pro_detail_btn"> <a href="#order" class="prodtl_btn1">產(chǎn)品咨詢</a><a href="/contact.html" target="_blank" class="prodtl_btn2">聯(lián)系我們</a> </div> </div> <div id="x4vfcpe" class="clear"></div> </div>  <div class="x4vfcpe" id="ny_pro_box02"> <div class="x4vfcpe" id="con"> <ul id="tags"> <li id="x4vfcpe" class=selectTag><A onmouseover="selectTag('tagContent0',this)" href="javascript:void(0)"onFocus="this.blur()">產(chǎn)品介紹：</A> </li> </ul> <div class="x4vfcpe" id=tagContent> <div id="x4vfcpe" class="tagContent selectTag" id=tagContent0><p>SNP（single nucleotide polymorphism）原理</p><p> SNP（single nucleotide polymorphism），即單核苷酸多態(tài)，是由于單個核苷酸改變而導(dǎo)致的核酸序列多態(tài)。一般來說，一個SNP位點只有兩種等位基因，因此又叫雙等位基因。SNP在人基因組中的發(fā)生頻率比較高，大約平均每1000個堿基中就有一個多態(tài)位點，是繼微衛(wèi)星之后的第三代遺傳標(biāo)記。有些SNP位點還會影響基因的功能，從而導(dǎo)致生物性狀改變甚至致病。SNP廣泛用于群體遺傳學(xué)研究（如生物的起源、進(jìn)化及遷移等方面，將逐漸取代微衛(wèi)星而成為新一代的分子生物學(xué)標(biāo)記）和疾病相關(guān)基因的研究，在藥物基因組學(xué)、診斷學(xué)和生物醫(yī)學(xué)研究中起重要作用。</p><p>SNP（single nucleotide polymorphism）服務(wù)流程</p><p>Taqman/MGB探針法</p><p><img alt="" src="https://img51.chem17.com/gxhpic_33572a5ad1/34139391ea0c7f8fbbc9db1a4d4515272b239c0ada76adc9bf8a4468728dba9daf2ddf1880e64d35.jpg" /></p><p>1. 客戶提供：</p><p>1）.已純化基因組DNA，并填寫詳細(xì)基因組DNA量，濃度及純度。</p><p>2）.或提供新鮮的組織，血液，細(xì)胞樣本；且盡量多的材料。</p><p>3）.提供已知的基因序列或物種基因序列號；盡可能詳細(xì)的背景資料。</p><p>2. 針對客戶要求的特定DNA序列區(qū)域，將為客戶提供引物和Taqman探針的設(shè)計和合成。</p><p>3. 提供新鮮的組織，血液，細(xì)胞樣本等抽提出RNA后，進(jìn)行反轉(zhuǎn)錄成cDNA。</p><p>4. 以DNA為模板，對目的基因進(jìn)行熒光定量PCR檢測。</p><p>5. 實驗數(shù)據(jù)分析。</p><p>6. 提供：峰圖文件（abl.格式），序列文件（seq.格式）；正式的數(shù)據(jù)分析報告。</p><p><img alt="" src="https://img55.chem17.com/gxhpic_33572a5ad1/34139391ea0c7f8fbbc9db1a4d451527e3fbcdc082b712df369e9ef2c8582feb131fdcee90a44561.jpg" /></p><p>樣本運(yùn)輸：</p><p> 客戶根據(jù)溫度，所在區(qū)域及樣本類型的差異，以加冰袋或干冰運(yùn)輸，并保證樣本的密封性和完整性，以免造成不必要的污染和損耗。</p></div> <div class="x4vfcpe" id="nr_textbox"><link rel="stylesheet" type="text/css" href="/css/MessageBoard_style.css"> <script language="javascript" src="/skins/Scripts/order.js?v=20210318" type="text/javascript"></script> <a name="order" id="order"></a> <div id="x4vfcpe" class="ly_msg" id="ly_msg"> <form method="post" name="form2" id="form2"> <h3>留言框 </h3> <ul> <li> 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