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src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138171486404346/6371381714864043466859489.jpg" class="vcenter" onerror="javascript:this.src='/static/new_net_01/images/nopic.jpg';"></p></div></div><div id="3gi82w9" class="smallimg"><div><p class="pic"><img src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138171486404346/6371381714864043466859489.jpg" class="vcenter" onerror="javascript:this.src='/static/new_net_01/images/nopic.jpg';"></p></div></div></div><div id="gkh3k3l" 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>山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià),蛋白純化系統(tǒng)</p><p><span>***更新：</span>2020-07-31 23:04:38</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="s3szbsu" 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="7g3lfmt" class="page-proshow02"><p class="title">詳細(xì)說明</p><div id="2uoam7n" 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)，山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià)，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，山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià)，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)溶劑會破壞蛋白質(zhì)表面的水化層，促使蛋白質(zhì)分子變得不穩(wěn)定而析出，山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià)。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.山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià)</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià),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">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。四川化學(xué)分析蛋白純化系統(tǒng)廠家報(bào)價(jià)</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià),蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138171347973309/6371381713479733098214210.jpg"></div><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><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(xiàng)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。</p><div style="width:100%;text-align: center;"><img style="max-width: 640px; max-height: 320px;" alt="山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià),蛋白純化系統(tǒng)" src="http://tyunfile.71360.com/UpLoadFile/szyss/2020/1/637138172282251484/6371381722822514847644105.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。四川化學(xué)分析蛋白純化系統(tǒng)廠家報(bào)價(jià)</p><p style="text-indent:25px">山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià)</p><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，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。山東智能蛋白純化系統(tǒng)廠家報(bào)價(jià)</p><p style="text-indent:25px">蘇州英賽斯智能科技有限公司于2017-01-09成立，注冊資本200-300萬元元，現(xiàn)有專業(yè)技術(shù)人員11~50人人，各種專業(yè)人員齊備。致力于創(chuàng)造***的產(chǎn)品與服務(wù)，以誠信、敬業(yè)、進(jìn)取為宗旨，以建Inscinstech明星產(chǎn)品為目標(biāo)，努力打造成為同行業(yè)中具有影響力的企業(yè)。我公司擁有強(qiáng)大的技術(shù)實(shí)力，多年來一直專注于機(jī)器人與自動化設(shè)備、機(jī)械電子設(shè)備的研發(fā)、生產(chǎn)、銷售及技術(shù)咨詢；光學(xué)檢測設(shè)備、光電產(chǎn)品研發(fā)、制造、銷售；實(shí)驗(yàn)室設(shè)備、儀器儀表的研發(fā)、制造、銷售及提供相關(guān)的技術(shù)咨詢和售后服務(wù)；自營和代理各類商品及技術(shù)的進(jìn)出口業(yè)務(wù)（限定企業(yè)經(jīng)營或禁止進(jìn)出口的商品和技術(shù)除外）。（依法需經(jīng)批準(zhǔn)的項(xiàng)目，經(jīng)相關(guān)部門批準(zhǔn)后方可開展經(jīng)營活動）的發(fā)展和創(chuàng)新，打造高指標(biāo)產(chǎn)品和服務(wù)。蘇州英賽斯智能科技有限公司主營業(yè)務(wù)涵蓋[ "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" ]，堅(jiān)持“質(zhì)量***、質(zhì)量服務(wù)、顧客滿意”的質(zhì)量方針，贏得廣大客戶的支持和信賴。</p></p><br /><p>文章來源地址: http://www.cdcfah.com/cp/767361.html</p></div></div></div></div></div><div id="yfw323h" class="page-right twoColRt"><div id="bfs7ram" class="box01 margin10 clearfix"><h3><a 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