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MTX-PEG-Cy3

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Catalog No. T203560

MTX-PEG-Cy3 is a Cy3-labeled MTX-PEG conjugate. Cy3 fluorophore is frequently utilized in applications such as immunolabeling, nucleic acid labeling, fluorescence microscopy, and flow cytometry, with a maximum emission wavelength of approximately 562-570 nm. Methotrexate (Amethopterin; MTX) serves as an antimetabolite and antifolate agent that inhibits dihydrofolate reductase, preventing the conversion of folic acid to tetrahydrofolate and ultimately inhibiting DNA synthesis. Additionally, Methotrexate functions as an immunosuppressant and antineoplastic agent, deployed in the treatment of rheumatoid arthritis and the investigation of various cancers, including acute lymphoblastic leukemia.

MTX-PEG-Cy3

MTX-PEG-Cy3

😃Good
Catalog No. T203560
MTX-PEG-Cy3 is a Cy3-labeled MTX-PEG conjugate. Cy3 fluorophore is frequently utilized in applications such as immunolabeling, nucleic acid labeling, fluorescence microscopy, and flow cytometry, with a maximum emission wavelength of approximately 562-570 nm. Methotrexate (Amethopterin; MTX) serves as an antimetabolite and antifolate agent that inhibits dihydrofolate reductase, preventing the conversion of folic acid to tetrahydrofolate and ultimately inhibiting DNA synthesis. Additionally, Methotrexate functions as an immunosuppressant and antineoplastic agent, deployed in the treatment of rheumatoid arthritis and the investigation of various cancers, including acute lymphoblastic leukemia.
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Product Introduction

Bioactivity
Description
MTX-PEG-Cy3 is a Cy3-labeled MTX-PEG conjugate. Cy3 fluorophore is frequently utilized in applications such as immunolabeling, nucleic acid labeling, fluorescence microscopy, and flow cytometry, with a maximum emission wavelength of approximately 562-570 nm. Methotrexate (Amethopterin; MTX) serves as an antimetabolite and antifolate agent that inhibits dihydrofolate reductase, preventing the conversion of folic acid to tetrahydrofolate and ultimately inhibiting DNA synthesis. Additionally, Methotrexate functions as an immunosuppressant and antineoplastic agent, deployed in the treatment of rheumatoid arthritis and the investigation of various cancers, including acute lymphoblastic leukemia.
Chemical Properties
Storage & Solubility Information
Storagekeep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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