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class="pic"><img src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138172377738528/6371381723777385289828518.jpg" class="vcenter" onerror="javascript:this.src='/static/new_net_01/images/nopic.jpg';"></p></div></div><div id="odfxzqx" class="smallimg"><div><p class="pic"><img src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138172377738528/6371381723777385289828518.jpg" class="vcenter" onerror="javascript:this.src='/static/new_net_01/images/nopic.jpg';"></p></div></div></div><div id="wq3qa2w" class="content"><p><span>需求數(shù)量：</span>0</p><p><span>價(jià)格要求：</span>面議</p><p><span>所在地：</span>江蘇省</p><p><span>包裝要求：</span><span style="color: #f30;"></span></p><p><span>產(chǎn)品關(guān)鍵詞：</span>蛋白純化系統(tǒng)***的選擇,蛋白純化系統(tǒng)</p><p><span>***更新：</span>2020-08-11 06:02:56</p><p><span id="click" >瀏覽次數(shù)：0次</span></p><a rel="nofollow" class="button">聯(lián)系我們</a></div></div><div id="mbvcuoq" class="rightbox"><h3>公司基本資料信息</h3><p style="border:0;"><a rel="nofollow">蘇州英賽斯智能科技有限公司</a></p><p><span>聯(lián)系人：</span>李大為</p><p><span>郵箱: </span>570745634@qq.com</p><p><span>電話: </span>18606243033</p><p><span>傳真: </span>0512_63937379</p><p><span>網(wǎng)址: </span>http://www.inscinstech.com.cn</p><p><span>手機(jī): </span>0512-63937378</p><p><span>地址: </span>吳江經(jīng)濟(jì)技術(shù)開發(fā)區(qū)聯(lián)楊路南側(cè)、龍橋路西側(cè)</p><p>[當(dāng)前離線] <a rel="nofollow"> [加為商友] </a><a rel="nofollow"> [發(fā)送信件] </a></p></div></div><div id="sxpc3q8" class="page-proshow02"><p class="title">詳細(xì)說明</p><div id="hbtqipr" class="box"><p><p style="text-indent:25px">蛋白質(zhì)分離純化步驟（二） 2.2 蛋白質(zhì)的抽提通常選擇適當(dāng)?shù)木彌_液溶劑把蛋白質(zhì)提取出來。抽提所用緩沖液的pH、離子強(qiáng)度、組成成分等條件的選擇應(yīng)根據(jù)欲制備的蛋白質(zhì)的性質(zhì)而定。如膜蛋白的抽提，抽提緩沖液中一般要加入表面活性劑（十二烷基磺酸鈉、tritonX-100等），使膜結(jié)構(gòu)破壞，利于蛋白質(zhì)與膜分離。在抽提過程中，應(yīng)注意溫度，避免劇烈攪拌等，以防止蛋白質(zhì)的變性。 2.3蛋白質(zhì)粗制品的獲得選用適當(dāng)?shù)姆椒▽⑺牡鞍踪|(zhì)與其它雜蛋白分離開來，蛋白純化系統(tǒng)***的選擇。比較方便的有效方法是根據(jù)蛋白質(zhì)溶解度的差異進(jìn)行的分離。常用的有下列幾種方法： 1. 等電點(diǎn)沉淀法不同蛋白質(zhì)的等電點(diǎn)不同，可用等電點(diǎn)沉淀法使它們相互分離。 2. 鹽析法不同蛋白質(zhì)鹽析所需要的鹽飽和度不同，所以可通過調(diào)節(jié)鹽濃度將目的蛋白沉淀析出。被鹽析沉淀下來的蛋白質(zhì)仍保持其天然性質(zhì)，并能再度溶解而不變性。 3. 有機(jī)溶劑沉淀法中性有機(jī)溶劑如乙醇、**，它們的介電常數(shù)比水低。能使大多數(shù)球狀蛋白質(zhì)在水溶液中的溶解度降低，蛋白純化系統(tǒng)***的選擇，進(jìn)而從溶液中沉淀出來，因此可用來沉淀蛋白質(zhì)。此外，有機(jī)溶劑會(huì)破壞蛋白質(zhì)表面的水化層，蛋白純化系統(tǒng)***的選擇，促使蛋白質(zhì)分子變得不穩(wěn)定而析出。由于有機(jī)溶劑會(huì)使蛋白質(zhì)變性，使用該法時(shí)，要注意在低溫下操作.蛋白純化系統(tǒng)***的選擇</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="蛋白純化系統(tǒng)***的選擇,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138172377738528/6371381723777385289828518.jpg"></div><p> 蛋白質(zhì)純化方法-親和層析親和層析法包括特異性配體親和層析法以及通用性配體親和層析法。比較這兩種親和層析法。特異性配體親和層析法通常將復(fù)雜的生命大分子物質(zhì)作為配體，它的結(jié)合力比較大河吸附選擇性比較強(qiáng)。而通用性配體親和層析法通常將簡單的小分子物質(zhì)作為配體，因此，它具有低廉的成本，吸附容量比較高，通過對吸附和脫附條件的改善能夠使得層析的分辨率提高。原理親和層析的原理類似于酶-底物，***-受體與抗原-抗體等特異性反應(yīng)的機(jī)理。有一定的親和力在每對反應(yīng)物之間。與在酶與底物的反應(yīng)中，只有特異的底物才可以結(jié)合一定的酶，使復(fù)合物產(chǎn)生相同。在親和層析中，只有特異的配體才可以和一定的生命大分子有親和力，并且使復(fù)合物產(chǎn)生。親和層析配體呈固相，而酶與底物的反應(yīng)底物呈液相是它們的不同點(diǎn)。事實(shí)上，親和層析是在含有活化基團(tuán)的基質(zhì)M上以共價(jià)鍵的方式固化具有識別能力的配體L，將固相載體制作成功而固化后的配體束縛特異物質(zhì)的能力依然保持。所以當(dāng)在小層析柱裝入固相載體，使得欲分離的樣品在該柱經(jīng)過。此時(shí)，樣品中對配體有親和力的物質(zhì)S就能夠通過結(jié)構(gòu)互補(bǔ)效應(yīng)、范德瓦爾力與靜電引力等作用在固相載體上吸附著。蛋白純化系統(tǒng)***的選擇</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="蛋白純化系統(tǒng)***的選擇,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138171486404346/6371381714864043466859489.jpg"></div><p style="text-indent:25px">三、蛋白質(zhì)分子量的測定蛋白質(zhì)分子量測定的方法很多，目前常用的方法有以下幾種。 3.1 凝膠過濾法凝膠過濾法測定蛋白質(zhì)分子量的原理如“分離純化方法”中所述。一定型號的凝膠顆粒上具有一定大小的孔隙，只允許較小的分子進(jìn)入膠粒，而大于孔隙的分子則不能進(jìn)入膠粒而被排阻在膠粒外面。用洗脫液洗脫時(shí)，被排阻的分子量大的蛋白質(zhì)先被洗脫下來，隨后能夠進(jìn)入顆粒的蛋白質(zhì)也按分子量大小而先后被洗脫下來，分子量越小的越后被洗脫下來。由于不同排阻范圍的葡聚糖凝膠有一特定的蛋白質(zhì)分子量范圍，在此范圍內(nèi)，分子量的對數(shù)和洗脫體積之間成線性關(guān)系。因此，用幾種已知分子量的蛋白質(zhì)為標(biāo)準(zhǔn)進(jìn)行層析分析，以每種蛋白質(zhì)的洗脫體積對它們的分子量的對數(shù)作圖，繪制出標(biāo)準(zhǔn)洗脫曲線。未知蛋白質(zhì)在同樣的條件下進(jìn)行層析分析，根據(jù)其所用的洗脫體積，從標(biāo)準(zhǔn)洗脫曲線上可求出此未知蛋白質(zhì)對應(yīng)的分子量來。</p><p style="text-indent:25px">三、蛋白質(zhì)分子量的測定 3.3 沉降法沉降法又稱超速離心法。蛋白質(zhì)溶液在受到強(qiáng)大的離心力作用時(shí)，蛋白質(zhì)分子趨于下沉，沉降速度與蛋白質(zhì)分子的大小、密度和分子形狀有關(guān)，也與溶劑的密度和粘度有關(guān)。蛋白質(zhì)顆粒在離心場中的沉降速度用每單位時(shí)間內(nèi)顆粒下沉的距離來表示。在離心場中，蛋白質(zhì)分子所受到的凈離心力（離心力減去浮力）與溶劑的摩擦力平衡時(shí)，每單位離心場強(qiáng)度的沉降速度稱為沉降系數(shù)（Sedimentation Coefficient）。國際上采用Svedberg單位作為沉降系數(shù)的單位，用S表示，以紀(jì)念超速離心法的創(chuàng)始人，瑞典***的蛋白質(zhì)化學(xué)家T.Svedberg。一個(gè)Svedberg單位（或直接稱一個(gè)S）為1×10—13s。蛋白質(zhì)的沉降系數(shù)大約在1×10—13～200×10—13s范圍內(nèi)，即1S～200S。</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="蛋白純化系統(tǒng)***的選擇,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138171759963463/6371381717599634633342360.jpg"></div><p style="text-indent:25px">蛋白質(zhì)分離純化步驟（二） 2.4.2 纖維素柱層析法該法是利用蛋白質(zhì)的酸堿性質(zhì)作為分離的基礎(chǔ)。離子交換纖維素（cellulose ion-exchanger）是人工合成的纖維素衍生物，它具有松散的親水性網(wǎng)狀結(jié)構(gòu)，有較大的表面積，使蛋白質(zhì)大分子可以自由通過。因此常用于蛋白質(zhì)的分離。（1）羧甲基纖維素（CM-纖維素）在纖維素顆粒上帶有羧甲基基團(tuán)。在中性pH條件下，羧甲基上的質(zhì)子可解離下來（圖2-27a），而溶液中帶正電荷的蛋白質(zhì)分子可與纖維素顆粒上的羧甲基負(fù)電荷結(jié)合?？山粨Q的基團(tuán)帶正電，因此是一種陽離子交換劑。蛋白質(zhì)與離子交換纖維素之間結(jié)合能力的大小取決于彼此間相反電荷基團(tuán)之間靜電吸引。 (2）二乙氨基乙基纖維素（DEAE-纖維素）在中性pH條件下，它含有帶正電荷的基團(tuán)，可與溶液中的帶負(fù)電荷的蛋白質(zhì)結(jié)合，可交換的基團(tuán)帶負(fù)電荷，因此是一種陰離子交換劑。當(dāng)某一蛋白質(zhì)混合溶液通過裝有DEAE-纖維素的層析柱時(shí)，帶正電荷的蛋白質(zhì)不能結(jié)合而隨著洗脫液的流動(dòng)先被洗脫下來。帶負(fù)電荷的蛋白質(zhì)將被結(jié)合到柱上。結(jié)合力取決于彼此相反電荷基團(tuán)間的靜電吸引。然后選用一定pH和離子強(qiáng)度的緩沖液進(jìn)行洗脫，改變蛋白質(zhì)分子所帶的靜電荷，依次從層析柱流出達(dá)到相互分離的目的。蛋白純化系統(tǒng)***的選擇</p><p style="text-indent:25px">蛋白純化系統(tǒng)***的選擇</p><p style="text-indent:25px">在人類社會(huì)進(jìn)入知識經(jīng)濟(jì)時(shí)代、信息技術(shù)高速發(fā)展的背景下，儀器儀表及其測量控制技術(shù)得到日益***應(yīng)用，給儀器儀表行業(yè)的快速發(fā)展提供了良好契機(jī)。經(jīng)過近十年來的建設(shè)與發(fā)展，我國儀器儀表已經(jīng)初步形成產(chǎn)品門類品種比較齊全，具有一定生產(chǎn)規(guī)模和開發(fā)能力的產(chǎn)業(yè)體系，成為亞洲除日本以外第二大儀器儀表生產(chǎn)國。進(jìn)一步提升我國儀器儀表技術(shù)和水平，其他內(nèi)資企業(yè)企業(yè)要順應(yīng)產(chǎn)業(yè)發(fā)展潮流，在穩(wěn)固常規(guī)品種的同時(shí)，進(jìn)一步發(fā)展智能儀器儀表，提升產(chǎn)業(yè)數(shù)字化、智能化、集成化水平。工業(yè)領(lǐng)域轉(zhuǎn)型升級、提升發(fā)展質(zhì)量等有利于儀器儀表行業(yè)的發(fā)展；**安全、社會(huì)安全、產(chǎn)業(yè)和信息安全等需要自主、[ "蛋白純化色譜系統(tǒng)", "凝膠凈化色譜系統(tǒng)", "制備液相色譜", "柱塞泵" ]裝備，成為全社會(huì)共識；我國生產(chǎn)型發(fā)展迅速，年均增長速度超過20%。在相關(guān)報(bào)告中可以***了解到在我國工業(yè)基礎(chǔ)生產(chǎn)型產(chǎn)業(yè)現(xiàn)狀研究的成果。蛋白純化系統(tǒng)***的選擇</p><p style="text-indent:25px">蘇州英賽斯智能科技有限公司創(chuàng)辦于2017-01-09，是一家生產(chǎn)型的公司。經(jīng)過多年不斷的歷練探索和創(chuàng)新發(fā)展，是一家其他內(nèi)資企業(yè)企業(yè)，隨著市場的發(fā)展和生產(chǎn)的需求，與多家企業(yè)合作研究，在原有產(chǎn)品的基礎(chǔ)上經(jīng)過不斷改進(jìn)，追求新型，在強(qiáng)化內(nèi)部管理，完善結(jié)構(gòu)調(diào)整的同時(shí)，優(yōu)良的質(zhì)量、合理的價(jià)格、完善的服務(wù)，在業(yè)界受到***好評。公司始終堅(jiān)持客戶需求***的原則，致力于提供高質(zhì)量的[ "蛋白純化色譜系統(tǒng)", "凝膠凈化色譜系統(tǒng)", "制備液相色譜", "柱塞泵" ]。英賽斯以創(chuàng)造***產(chǎn)品及服務(wù)的理念，打造高指標(biāo)的服務(wù)，引導(dǎo)行業(yè)的發(fā)展。</p></p><br /><p>文章來源地址: http://m.cdcfah.com/cp/877208.html</p></div></div></div></div></div><div id="ti3e3lf" class="page-right twoColRt"><div id="7v0jiev" class="box01 margin10 clearfix"><h3><a href="http://m.cdcfah.com/cp/">猜你喜歡</a></h3><div id="4ga33ug" class="recomPic likePro"><a href="http://m.cdcfah.com/cp/814588.html"><div><img 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