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id="n837e3l" 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)上門維修,蛋白純化系統(tǒng)</p><p><span>***更新：</span>2020-08-21 07:01:40</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="yzl8qkg" 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="crtvx3t" class="page-proshow02"><p class="title">詳細(xì)說明</p><div id="ncel3wy" class="box"><p><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，江蘇樣品前處理蛋白純化系統(tǒng)上門維修，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，江蘇樣品前處理蛋白純化系統(tǒng)上門維修，江蘇樣品前處理蛋白純化系統(tǒng)上門維修。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。江蘇樣品前處理蛋白純化系統(tǒng)上門維修</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)上門維修,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138171935864644/6371381719358646441189533.jpg"></div><p style="text-indent:25px">蛋白質(zhì)分離純化步驟蛋白質(zhì)分離純化的一般原則：大多數(shù)蛋白質(zhì)在組織細(xì)胞中都是和核酸等生物分子結(jié)合在一起，而且每種類型的細(xì)胞都含有成千上萬種不同的蛋白質(zhì)。許多蛋白質(zhì)在結(jié)構(gòu)、性質(zhì)上有許多相似之處，所以蛋白質(zhì)的分離提純是一項復(fù)雜的工作。到目前為止，還沒有一**成的方法能把任何一種蛋白質(zhì)從復(fù)雜的混合物中提取出來。但是對于任何一種蛋白質(zhì)都有可能選擇一種較合適的分離純化程序以獲得高純度的制品。且分離的關(guān)鍵步驟、基本手段還是共同的。蛋白質(zhì)提純的目的是增加產(chǎn)品的純度和產(chǎn)量，同時又要保持和提高產(chǎn)品的生物活性。因此，要分離純化某一種蛋白質(zhì)，首先應(yīng)選擇一種含目的蛋白質(zhì)較豐富的材料。其次，應(yīng)設(shè)法避免蛋白質(zhì)變性，以制備有活性的蛋白質(zhì)。對于大多數(shù)蛋白質(zhì)來說，純化操作都是在0～4℃的低溫下進(jìn)行的。同時也應(yīng)避免過酸、過堿的條件以及劇烈的攪拌和振蕩。另外，還要設(shè)法除去變性的蛋白質(zhì)和其它雜蛋白，從而達(dá)到增加純度和提高產(chǎn)量的目的。江蘇樣品前處理蛋白純化系統(tǒng)上門維修</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)上門維修,蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2019/8/637020707435096926/6370207074350969265706238.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。</p><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。</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)上門維修,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">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，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。江蘇樣品前處理蛋白純化系統(tǒng)上門維修</p><p style="text-indent:25px">江蘇樣品前處理蛋白純化系統(tǒng)上門維修</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。江蘇樣品前處理蛋白純化系統(tǒng)上門維修</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。公司是一家其他內(nèi)資企業(yè)企業(yè)，以誠信務(wù)實的創(chuàng)業(yè)精神、質(zhì)量高速的管理團(tuán)隊、精悍的職工隊伍，努力為廣大用戶提供***的產(chǎn)品。公司目前擁有優(yōu)異員工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" ]等多項業(yè)務(wù)。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://www.cdcfah.com/cp/988065.html</p></div></div></div></div></div><div id="vfmtamo" class="page-right twoColRt"><div id="lls3o2g" class="box01 margin10 clearfix"><h3><a href="http://www.cdcfah.com/cp/">猜你喜歡</a></h3><div id="tnkwipg" class="recomPic likePro"><a href="http://www.cdcfah.com/cp/814588.html"><div><img 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