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當(dāng)前位置:首頁(yè)  >  技術(shù)文章  >  【設(shè)備更新】手動(dòng)ITC升級(jí)到全自動(dòng)ITC,分析效率提升7倍!

【設(shè)備更新】手動(dòng)ITC升級(jí)到全自動(dòng)ITC,分析效率提升7倍!

更新時(shí)間:2024-04-18       點(diǎn)擊次數(shù):397

國(guó)務(wù)院推動(dòng)大規(guī)模設(shè)備更新的方案已經(jīng)在各地穩(wěn)步推行,其中提升教學(xué)科研水平的教育科研設(shè)備備受關(guān)注。

分析儀器智能化、自動(dòng)化作為提高分析檢測(cè)能力的主要方向,也十分契合國(guó)家推行設(shè)備更新的“鼓勵(lì)先進(jìn)、淘汰落后”的總體要求。馬爾文帕納科有多款設(shè)備均可以進(jìn)行自動(dòng)化升級(jí),本文中我們將對(duì)溶液內(nèi)分子互作的金標(biāo)準(zhǔn)技術(shù):等溫滴定量熱技術(shù)(ITC)的自動(dòng)化升級(jí)進(jìn)行介紹,您將看到ITC用戶的分析效率如何數(shù)倍的提升!

 

等溫滴定量熱儀(ITC)無需對(duì)樣品進(jìn)行任何標(biāo)記、無需芯片固定和修飾,也無需再生步驟,無分子量大小和樣品種類限制、是真正的無標(biāo)記的溶液內(nèi)互作技術(shù),被業(yè)內(nèi)認(rèn)可為分子間相互作用分析的金標(biāo)準(zhǔn)技術(shù)。馬爾文帕納科在Microcal PEAQ-ITC的基礎(chǔ)上,新增了全自動(dòng)化運(yùn)行的功能,推出Microcal PEAQ-ITC Automated系列,實(shí)現(xiàn)自動(dòng)化與智能化運(yùn)作,集高靈敏度與全自動(dòng)操作優(yōu)勢(shì)于一體。

 

圖片

PEAQ ITC (左),PEAQ-ITC Automated(右)

 


Microcal PEAQ-ITC Automated主要特點(diǎn)及優(yōu)勢(shì):

 

 

PEAQ-ITC Automated每天可分析高達(dá)42個(gè)滴定(按24小時(shí)計(jì)算),相比手動(dòng)版一般每天(按8小時(shí)計(jì)算)分析5個(gè)滴定,將分析效率提升7倍。全自動(dòng)化實(shí)現(xiàn)加樣,清洗,樣品轉(zhuǎn)移,減少人員操作誤差,減少新手培訓(xùn)和指導(dǎo)時(shí)間,提升數(shù)據(jù)質(zhì)量和儀器使用效率,把更多操作留給機(jī)器,將更多時(shí)間留給思考。

 

2024年,Microcal產(chǎn)品線中,Auto-ITC200系列、VP-ITC系列、VP-DSC系列、Cap-DSC系列將陸續(xù)停止服務(wù),馬爾文帕納科的經(jīng)典產(chǎn)品Mastersizer 2000也已于2022年停止服務(wù),為不影響您日常的研究、生產(chǎn)工作,我們建議您提前準(zhǔn)備在替代產(chǎn)品上的方法轉(zhuǎn)移。同時(shí)為響應(yīng)國(guó)家發(fā)改委推動(dòng)大規(guī)模設(shè)備更新的政策,我們將提供設(shè)備更新?lián)Q代的技術(shù)支持和測(cè)樣服務(wù),感興趣的用戶歡迎留下您的聯(lián)系方式,了解更多服務(wù)內(nèi)容。

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PEAQ-ITC Automated 相關(guān)文獻(xiàn)(部分):

1.Zong, Y. et al.Development of Complementary Photo‐arginine/lysine to Promote Discovery of Arg/Lys hPTMs Interactomes. Advanced Science2307526 (2024) doi:10.1002/advs.202307526.

2.Weng, Z. et al.Antimicrobial activities of lavandulylated flavonoids in Sophora flavences against methicillin-resistant Staphylococcus aureus via membrane disruption. Journal of Advanced Research57, 197–212 (2024).

3.Rivera, M. et al.A sensitive and scalable fluorescence anisotropy single stranded RNA targeting approach for monitoring riboswitch conformational states. Nucleic Acids Researchgkae118 (2024) doi:10.1093/nar/gkae118.

4.Ojha, M. et al.Structure of saguaro cactus virus 3′ translational enhancer mimics 5′ cap for eIF4E binding. Proc. Natl. Acad. Sci. U.S.A.121, e2313677121 (2024).

5.Choi, Y., Koh, J., Cha, S.-S. & Roe, J.-H. Activation of zinc uptake regulator by zinc binding to three regulatory sites. Nucleic Acids Researchgkae079 (2024) doi:10.1093/nar/gkae079.

6.Travis, C. R., Francis, D. Y., Williams, D. C. & Waters, M. L. Evaluation of acyllysine isostere interactions with the aromatic pocket of the AF9YEATSdomain. Protein Science32, e4533 (2023).

7.Qiu, C. et al.Intra-and inter-molecular regulation by intrinsically-disordered regions governs PUF protein RNA binding. Nat Commun14, 7323 (2023).

8.Liu, S. et al.Differentiating Inhibition Selectivity and Binding Affinity of Isocitrate Dehydrogenase 1 Variant Inhibitors. J. Med. Chem.66, 5279–5288 (2023).

9.Campagne, S. et al.Molecular basis of RNA-binding and autoregulation by the cancer-associated splicing factor

RBM39. Nat Commun14, 5366 (2023).

10.Zeller, M. J. et al.SHAPE-enabled fragment-based ligand discovery for RNA. Proc. Natl. Acad. Sci. U.S.A.119, e2122660119 (2022).

11.Feng, T. et al.Adipocyte-derived lactate is a signalling metabolite that potentiates adipose macrophage inflammation via targeting PHD2. Nat Commun13, 5208 (2022).

12.Zhou, J., Horton, J. R., Blumenthal, R. M., Zhang, X. & Cheng, X. Clostridioides difficile specific DNA adenine methyltransferase CamA squeezes and flips adenine out of DNA helix. Nat Commun12, 3436 (2021).

13.Palte, R. L. et al.Cryo-EM structures of inhibitory antibodies complexed with arginase 1 provide insight into mechanism of action. Commun Biol4, 927 (2021).

14.Liu, S. et al.Roles of metal ions in the selective inhibition of oncogenic variants of isocitrate dehydrogenase 1. Commun Biol4, 1243 (2021).

15.Chen, S., Zhang, W., Min, J. & Liu, K. Lesson from a Fab-enabled co-crystallization study of TDRD2 and PIWIL1. Methods175, 72–78 (2020).


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