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class="bigimg"><div><p class="pic"><img src="http://tyunfile.71360.com/UpLoadFile/szyss/2019/9/637045690922656965/6370456909226569652375876.png" class="vcenter" onerror="javascript:this.src='/static/new_net_01/images/nopic.jpg';"></p></div></div><div id="ktqxjqu" class="smallimg"><div><p class="pic"><img src="http://tyunfile.71360.com/UpLoadFile/szyss/2019/9/637045690922656965/6370456909226569652375876.png" class="vcenter" onerror="javascript:this.src='/static/new_net_01/images/nopic.jpg';"></p></div></div></div><div id="u7qikw2" class="content"><p><span>需求數(shù)量：</span>0</p><p><span>價格要求：</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>江蘇樣品前處理蛋白純化系統(tǒng)上門安裝,蛋白純化系統(tǒng)</p><p><span>***更新：</span>2020-08-10 22:04:28</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="22c32sz" 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="3jvxo87" class="page-proshow02"><p class="title">詳細(xì)說明</p><div id="4cegyf9" 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。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，進(jìn)而從溶液中沉淀出來，因此可用來沉淀蛋白質(zhì)。此外，江蘇樣品前處理蛋白純化系統(tǒng)上門安裝，有機(jī)溶劑會破壞蛋白質(zhì)表面的水化層，江蘇樣品前處理蛋白純化系統(tǒng)上門安裝，江蘇樣品前處理蛋白純化系統(tǒng)上門安裝，促使蛋白質(zhì)分子變得不穩(wěn)定而析出。由于有機(jī)溶劑會使蛋白質(zhì)變性，使用該法時，要注意在低溫下操作.江蘇樣品前處理蛋白純化系統(tǒng)上門安裝</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="江蘇樣品前處理蛋白純化系統(tǒng)上門安裝,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2019/9/637045690922656965/6370456909226569652375876.png"></div><p style="text-indent:25px">蛋白質(zhì)分離純化步驟（二） 2.4 樣品的進(jìn)一步分離純化用等電點(diǎn)沉淀法、鹽析法所得到的蛋白質(zhì)一般含有其他蛋白質(zhì)雜質(zhì)，須進(jìn)一步分離提純才能得到有一定純度的樣品。常用的純化方法有：凝膠過濾層析、離子交換纖維素層析、親和層析等等。有時還需要這幾種方法聯(lián)合使用才能得到較高純度的蛋白質(zhì)樣品。 1. 凝膠過濾層析凝膠過濾層析（gel-filtration chromatography）又稱為分子排阻層析或分子篩層析。它是將葡聚糖凝膠（Sephadex）裝入一個柱子中，制成凝膠柱。這種凝膠顆粒具有網(wǎng)狀結(jié)構(gòu)，不同類型凝膠的網(wǎng)孔大小不同。當(dāng)把蛋白質(zhì)混合樣品加到凝膠柱中時，比凝膠網(wǎng)孔小的蛋白質(zhì)可進(jìn)入網(wǎng)孔內(nèi)，而大于網(wǎng)孔的分子則不能進(jìn)入被排阻在凝膠顆粒之外。當(dāng)用洗脫液洗脫時，被排阻的分子量大的蛋白質(zhì)直接通過凝膠之間的縫隙先被洗脫下來，而比網(wǎng)孔小的蛋白質(zhì)可連續(xù)不斷地進(jìn)入網(wǎng)孔內(nèi)。這樣的小分子不但流經(jīng)的路程長，而且受到來自凝膠內(nèi)部的阻力也很大，所以蛋白質(zhì)越小，從柱子上洗脫下來所需時間越長。由于不同蛋白質(zhì)的分子大小不同，進(jìn)入網(wǎng)孔的程度不同，因此流出的速度不同，洗脫所用體積及時間不同，從而達(dá)到分離的目的。樣品前處理化學(xué)分析蛋白純化系統(tǒng)</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="江蘇樣品前處理蛋白純化系統(tǒng)上門安裝,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138171674741306/6371381716747413062985954.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。可交換的基團(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，帶正電荷的蛋白質(zhì)不能結(jié)合而隨著洗脫液的流動先被洗脫下來。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。</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，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，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Svedberg單位（或直接稱一個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="江蘇樣品前處理蛋白純化系統(tǒng)上門安裝,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138172377738528/6371381723777385289828518.jpg"></div><p style="text-indent:25px">蛋白質(zhì)分離純化步驟（二）分離純化蛋白質(zhì)的一般程序 2.1 材料的預(yù)處理及細(xì)胞破碎分離提純某一種蛋白質(zhì)時，首先要把蛋白質(zhì)從組織或細(xì)胞中釋放出來并保持原來的天然狀態(tài)，不喪失活性。所以要采用適當(dāng)?shù)姆椒▽⒔M織和細(xì)胞破碎。常用的破碎組織細(xì)胞的方法有： 1. 機(jī)械破碎法這種方法是利用機(jī)械力的剪切作用，使細(xì)胞破碎。常用設(shè)備有，高速組織搗碎機(jī)、勻漿器、研缽等。 2. 滲透破碎法這種方法是在低滲條件使細(xì)胞溶脹而破碎。 3. 反復(fù)凍融法生物組織經(jīng)凍結(jié)后，細(xì)胞內(nèi)液結(jié)冰膨脹而使細(xì)胞脹破。這種方法簡單方便，但要注意那些對溫度變化敏感的蛋白質(zhì)不宜采用此法。 4. 超聲波法使用超聲波震蕩器使細(xì)胞膜上所受張力不均而使細(xì)胞破碎。 5. 酶法如用溶菌酶破壞微生物細(xì)胞等。江蘇蛋白純化系統(tǒng)廠家報(bào)價</p><p style="text-indent:25px">江蘇樣品前處理蛋白純化系統(tǒng)上門安裝</p><p style="text-indent:25px">在人類社會進(jìn)入知識經(jīng)濟(jì)時代、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)得到日益廣泛應(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。我國現(xiàn)有其他內(nèi)資企業(yè)企業(yè)數(shù)千多家，已經(jīng)形成門類品種比較齊全，具有一定技術(shù)基礎(chǔ)和生產(chǎn)規(guī)模的產(chǎn)業(yè)體系。但同時業(yè)內(nèi)**也指出，雖然我國測試儀器產(chǎn)業(yè)有了一定的發(fā)展，但遠(yuǎn)遠(yuǎn)不能滿足國民經(jīng)濟(jì)各行各業(yè)日益增長的迫切需求。[ "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" ]產(chǎn)業(yè)是國民經(jīng)濟(jì)的基礎(chǔ)性、戰(zhàn)略性產(chǎn)業(yè)，是信息化和工業(yè)化深度融合的源頭，對促進(jìn)工業(yè)轉(zhuǎn)型升級、發(fā)展戰(zhàn)略性新興產(chǎn)業(yè)、推動現(xiàn)代**建設(shè)、保障和提高人民生活水平具有重要作用。當(dāng)前正處于**開放40年之中國大變局，世界上只有一個救世主——市場，能救企業(yè)的只有你自己——自強(qiáng)，提高生產(chǎn)型核心競爭力才是中國制造業(yè)的***出路。以顯微科學(xué)儀器行業(yè)的發(fā)展與變化為例，以親身的實(shí)踐為例，毛磊認(rèn)為，**開放四十年，國家的環(huán)境和實(shí)力都發(fā)生了巨大變化，有了完全不同的基礎(chǔ)，這為國產(chǎn)科學(xué)儀器走向**增強(qiáng)了信心。江蘇樣品前處理蛋白純化系統(tǒng)上門安裝</p><p style="text-indent:25px">蘇州英賽斯智能科技有限公司成立于2017-01-09，注冊資本：200-300萬元。該公司生產(chǎn)型的公司。公司致力于為客戶提供安全、質(zhì)量有保障的質(zhì)量產(chǎn)品及服務(wù)，是一家其他內(nèi)資企業(yè)企業(yè)。公司目前擁有***員工11~50人人，具有[ "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" ]等多項(xiàng)業(yè)務(wù)。英賽斯自成立以來，一直堅(jiān)持走正規(guī)化、專業(yè)化路線，得到了廣大客戶及社會各界的普遍認(rèn)可與大力支持。</p></p><br /><p>文章來源地址: http://www.cdcfah.com/cp/874086.html</p></div></div></div></div></div><div id="bmda2w3" class="page-right twoColRt"><div id="irypryc" class="box01 margin10 clearfix"><h3><a 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