EZ Cap Mito-mScarlet Probe mRNA (m1Ψ)

EZ Cap Mito-mScarlet Probe mRNA (m1Ψ)

Author: ApexBio

shortsummary:

Mitochondria (Mito) probes mRNA with red fluorescent protein (mScarlet), modified by N1-Methylpseudo-UTP (m1Ψ), providing higher transcription efficiency and suppressing RNA-mediated innate immune activation.

phosphatase inhibitor cocktail 3

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In stock

Concanavalin A (Con A)-Biotin

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Dry ice

description:

Mito-mScarlet is a fusion protein, consisting of Mitochondria (Mito) localization sequence and red fluorescent protein (mScarlet). mScarlet is widely used in biological imaging due to its high brightness and rapid maturation. By fusing mScarlet with mitochondrial signal sequences, the dynamic changes of Mito can be observed in real time in living cells, helping to reveal the key role of Mito in energy metabolism, signal transduction and apoptosis. Mito-mScarlet simplifies the visualization process of Mito due to its efficient fluorescence properties and the advantages of Mito specific localization, and can more intuitively understand the role and behavior of Mito in the cell. EZ Cap Mito-mScarlet Probe mRNA (m1Ψ) is provided at a concentration of ~1 mg/ml with Cap1 structure. It is specifically used for the expression of red fluorescent protein markers in Mito. There are currently two ways to cap mRNA: One is co-transcription method, by adding Cap analogues into the transcription process. The other is enzymatic Capping. After transcription, Cap0 capping is performed by Vaccinia virus Capping Enzyme (VCE), GTP and S-adenosylmethionine (SAM). The Cap0 is then generated into the Cap1 through 2´-O-Methyltransferase and SAM. Cap1 Capping can also be performed by adding VCE, 2´-O-Methyltransferase, GTP and SAM in a one-step process. Cap 1 structure is more ideal for mammalian systems and possess higher transcription efficiency than Cap 0 structure. The addition of N1-Methylpseudo-UTP(m1Ψ) and poly(A) tail suppress RNA-mediated innate immune activation and increase the stability and lifetime of the mRNA in vitro and in vivo. Poly(A) tail also plays an important role in enhancing the efficiency of translation initiation.

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APExBIO Technology LLC is a premier provider of Small Molecule Inhibitors/Activators, Compound Libraries, Peptides, Assay Kits, Fluorescent Labels, Enzymes, Modified Nucleotides, mRNA synthesis and various tools for Molecular Biology. We carry a broad product line in over 25865 different research areas such as cancer, immunology, neurosciences, apoptosis and epigenetics etc. Based in USA (Houston, Texas), we have been serving the needs of customers across the world.