每得科技有限公司 Medclub Scientific Co., Ltd

每得科技有限公司 Medclub Scientific Co., Ltd 專營實驗室相關儀器及耗材http://www.medclub.com.tw * 免付費電話: 0800-007566 * 傳真: (03) 3279268

IDT DNA Oligo分裝服務上線自2026年5月1日起,IDT官網將推出DNA寡核苷酸分裝服務,支援客戶自訂配方與分裝需求。訂購時,只要在DNA Oligo輸入頁面的「Formulation」選單中,選擇「Create a custo...
01/05/2026

IDT DNA Oligo分裝服務上線

自2026年5月1日起,IDT官網將推出DNA寡核苷酸分裝服務,支援客戶自訂配方與分裝需求。

訂購時,只要在DNA Oligo輸入頁面的「Formulation」選單中,選擇「Create a custom formulation」,即可依需求設定單管或多管分裝,並儲存為常用配方,方便後續訂購。

對於需要固定配方、多管分裝,或希望減少反覆凍融的實驗室來說,這項更新能讓DNA oligo訂購流程更加快速便利。

自訂配方與分裝服務可能依規格產生額外費用,歡迎洽詢每得科技協助確認。
了解多點:
https://www.medclub.com.tw/product_1712457.html

每得科技 Medclub Scientific
IDT台灣代理

#每得科技 #寡核苷酸 #分子生物學 #實驗室耗材

IDT has been a driving force in the   market since the earliest days of the field. From sample to sequencer, our end to ...
30/04/2026

IDT has been a driving force in the market since the earliest days of the field. From sample to sequencer, our end to end capabilities and deep expertise continue to enable innovation and help shape the future landscape. Read more from President Ajay Gannerkote here: https://www.medclub.com.tw/hot_532547.html

What would it take to decentralize CAR-T therapy in Europe?One example is the ARI program at Hospital Clínic de Barcelon...
28/04/2026

What would it take to decentralize CAR-T therapy in Europe?
One example is the ARI program at Hospital Clínic de Barcelona, where researchers are developing and manufacturing CAR-T therapies directly within the hospital setting.

Sharing a recap from our Bridging the Gap webinar discussion exploring how initiatives like this could help expand access to advanced therapies and reshape the future of cell therapy.


Thank you to Manel Juan and Sergio Navarro Velázquez.
Take a look 👇
https://www.medclub.com.tw/hot_532585.html

We are extremely proud to announce our entry into the NGS in vitro diagnostics (IVD) market. Introducing Archer FUSIONPl...
23/04/2026

We are extremely proud to announce our entry into the NGS in vitro diagnostics (IVD) market. Introducing Archer FUSIONPlex™-HT Dx and VARIANTPlex™-HT Dx. These solutions will equip molecular pathologists with compliant in vitro diagnostics, without compromising innovation: https://www.medclub.com.tw/hot_532571.html

Pathlength correction is a stable and reliable technique that eliminates physical differences between different sample v...
21/04/2026

Pathlength correction is a stable and reliable technique that eliminates physical differences between different sample volumes, enabling comparability of high-throughput data. It also allows for unified calibration of microplate results with data from 1cm standard optical path cuvettes. Based on pre-calibrated K-factors and the molar extinction coefficients of the analytes, this method can directly calculate sample concentrations without relying on standard curves for calibration. CLUBIO Feyond series microplate reader and ReaderIt analysis software combination is an excellent analytical tool. Furthermore, the Feyond series microplate reader can be paired with the uNano ultra-micro plate, with sample loading volumes as low as 2µL, and 16/96-well throughput options, allowing for direct quantification of DNA, RNA, and protein concentrations without complex conversions.
https://www.medclub.com.tw/hot_532551.html

We’re excited to unveil IDT’s latest   innovation roadmap—purpose-built to accelerate cancer breakthroughs and empower r...
16/04/2026

We’re excited to unveil IDT’s latest innovation roadmap—purpose-built to accelerate cancer breakthroughs and empower researchers working at the forefront of precision . 👏

Read more here: https://www.medclub.com.tw/hot_531476.html

Just before  , we’re reminded that although rare conditions affect smaller populations, together they represent one of t...
14/04/2026

Just before , we’re reminded that although rare conditions affect smaller populations, together they represent one of the largest unmet needs in global health. Personalized is opening doors for patients with ultra-rare diseases—conditions that have historically lacked research and treatment options. Demaris Mills, VP and GE of omics solutions at Danaher Corporation, shares how tailored therapies could transform care for the millions affected by rare diseases worldwide. Read more in Forbes Technology Council here: https://www.medclub.com.tw/hot_531481.html

In molecular biology experiments, the accurate detection of nucleic acid concentration and purity is a core prerequisite...
09/04/2026

In molecular biology experiments, the accurate detection of nucleic acid concentration and purity is a core prerequisite for the success of subsequent experiments such as PCR and gene sequencing. Excessively high concentrations may inhibit the reaction system, while excessively low concentrations can affect experimental sensitivity and even lead to direct experimental failure.
Currently, the mainstream methods for nucleic acid concentration detection are absorbance and fluorescence methods, with corresponding instruments including micro-spectrophotometers, fluorometers, and fluorescence microplate readers, respectively. Although they all output concentration values, their detection principles differ significantly, and they are suited to different application scenarios.
Today we'll take a comprehensive look at how to choose the right instruments for different scenarios and avoid common testing mistakes.

https://www.medclub.com.tw/hot_531446.html

Move beyond limitations! When complexity stops others, we keep going. We’ve partnered with Ansa Biotechnologies, Inc. to...
07/04/2026

Move beyond limitations! When complexity stops others, we keep going. We’ve partnered with Ansa Biotechnologies, Inc. to provide you with long, complex clonal DNA up to 50 kb. Expect fast turnaround, dependable delivery, and sequence-perfect DNA, so your boldest ideas don’t have to wait. Learn more here: https://www.medclub.com.tw/hot_531475.html

To ensure successful NGS library preparation, monitoring each step from sample preparation to sequencing library prepara...
02/04/2026

To ensure successful NGS library preparation, monitoring each step from sample preparation to sequencing library preparation is crucial. Understanding the expected results of different quality control steps, the GeneCE-100 biofragment analysis system not only provides users with a reference but also ensures the generation of high-quality libraries throughout the process—a core prerequisite for obtaining reliable sequencing data.

Read more: https://www.medclub.com.tw/hot_531440.html

At IDT, we’re helping transform the future of   drug development by enabling the rapid creation of personalized genetic ...
31/03/2026

At IDT, we’re helping transform the future of drug development by enabling the rapid creation of personalized genetic medicines. This impact came to life in the landmark treatment developed for Baby KJ—an infant with an ultrarare metabolic disease—demonstrating what’s possible when science, speed, and collaboration converge.

This breakthrough represents both a scientific milestone and an early look at a more responsive rare disease ecosystem—one where Danaher Corporation companies like IDT and Aldevron help make viable, scalable, and accessible.

We’re proud to contribute to this important work and to the innovation, partnership, and urgency driving new hope for more families, more conditions, and more breakthroughs ahead.

Read more about the new FDA plausible framework for rare disease drug development in The Scientist: https://www.medclub.com.tw/hot_531474.html

Multi-cancer early detection based on cfDNA shows great promise in improving the detection rate of early-stage cancers. ...
26/03/2026

Multi-cancer early detection based on cfDNA shows great promise in improving the detection rate of early-stage cancers. Among them, targeted sequencing methods that integrate DNA methylation and fragment omics features are particularly promising for clinical application as cfDNA-based early detection methods. This method is cost-effective and highly flexible, and will be further optimized with the development of technologies such as single-cell sequencing, ultra-deep sequencing, and machine learning.

https://www.medclub.com.tw/hot_531436.html

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