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Solar cell evaluation equipment and research reagents manufactured by Dyenamo, Sweden.

Interchemi Co., Ltd. is the agent for the Swedish company Dyenamo. We sell all products of Dyenamo.

Product list of Dyenamo, a Swedish company: - Photo-induced absorption spectroscopy (PIA) system - Dyenamo toolbox for investigation of complete DSSC devices - IPCE equipment for taking IPCE spectrum of solar cells - Potentiostat-based IV-measuring kit - High-sensitivity irradiance measurement kit - Dyenamo HT-holder for PEC measurements - DSSC (dye-sensitized solar cell) dyes (organic dyes, translucent aesthetic dyes, organic metal sensitizers like N719) - Perovskite precursors and additives, etc.

  • Analytical Equipment and Devices
  • Chemicals

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Novel coronavirus detection reagent

This is a new type of coronavirus detection reagent. RT-PCR method COVID-19 nucleic acid test EUA approved.

Detects the following genes: FAM for (2019-nCoV) ORF 1ab, ROX for N gene, CY5 for IC. Lysis buffer with Pathogen Inactivation including extraction and amplification reagent 24 test kits / BOX RT-PCR device is required. This is a reagent for research purposes.

  • Real-time PCR
  • RNA Purification Kit
  • Reverse transcriptase

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It is possible to introduce non-natural amino acids at targeted positions【CloverDirect】.

By simply adding this product to a cell-free translation system, you can efficiently synthesize proteins with non-natural amino acids in a short time.

○Quantitative: Non-natural amino acids can be introduced only at the desired position. ○Rapid and simple: Pinpoint labeled proteins can be obtained purified in about 2 hours. ○Variety: Non-natural amino acids labeled with fluorescence, biotin, etc., can be introduced.

  • Other protein analysis
  • Other research reagents
  • Other Protein Research

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Sterile Test Reagent BactFinder/FungiFinder

Contributing to cell safety!

Aseptic testing is generally required to be conducted using the final processed product as the test specimen, based on the aseptic testing method specified in the Japanese Pharmacopoeia General Test Method (4.06). This testing method requires a culture period of more than 14 days to obtain results. On the other hand, for specific cell processing products, it is desirable to obtain the results of the aseptic test before administration to the patient. However, due to the time required to obtain results from the pharmacopoeia-compliant aseptic test, it is often the case that test results are determined after administration. Additionally, for specific cell processing products, due to limitations such as the amount of specimen available and the time required for testing, it may not be possible to apply the aseptic testing method compliant with the pharmacopoeia. In such cases, consideration may be given to the "Rapid Microbial Testing Method" (as referenced in the 18th revision of the Japanese Pharmacopoeia). Our company has developed a rapid aseptic testing method using PCR that covers a wide range of microorganisms, including not only those listed in the pharmacopoeia but also environmental bacteria and human-derived bacteria, allowing for detection in a short time.

  • Real-time PCR

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