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<channel>
	<title>UTP &#8211; Tinzyme</title>
	<atom:link href="https://www.tinzyme.com/tag/utp/feed/" rel="self" type="application/rss+xml" />
	<link>https://www.tinzyme.com</link>
	<description>Enzymes, dNTP and rNTP</description>
	<lastBuildDate>Fri, 06 Jun 2025 06:35:04 +0000</lastBuildDate>
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		<title>Firefly Luciferase mRNA (N1-Me-Pseudo UTP)</title>
		<link>https://www.tinzyme.com/commercial-mrna/firefly-luciferase-mrna-n1-me-pseudo-utp/</link>
		
		<dc:creator><![CDATA[tinzyme]]></dc:creator>
		<pubDate>Mon, 08 May 2023 08:16:02 +0000</pubDate>
				<category><![CDATA[Commercial mRNA]]></category>
		<category><![CDATA[Luciferase]]></category>
		<category><![CDATA[Solution]]></category>
		<category><![CDATA[UTP]]></category>
		<guid isPermaLink="false">https://www.tinzyme.com/?p=4651</guid>

					<description><![CDATA[M050804 Firefly Luciferase mRNA N1 Me Pseudo UTP C...]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph"><strong>M050804, Firefly Luciferase mRNA (N1-Me-Pseudo UTP)</strong></p>



<p class="wp-block-paragraph"><strong>Product Description</strong></p>



<p class="wp-block-paragraph">Luciferase is a general term for the enzymes that can produce biofluorescence in nature, the most representative of which is from the North American fluorescent worm (Photinus pyralis). The sequence of the firefly Luciferase mRNA (N1 Me Pseudo UTP) is from Photinus pyralis, and point mutation is carried out on the basis of the wild type sequence, significantly improving the stability of the protein and the suitable pH range. Once the product enters the cell, it will express Luciferase, Luciferase can catalyze the oxidation of the substrate D-luciferin to oxyluciferin. In the process of D-luciferin oxidation, bioluminescence will be generated at about 560nm wavelength and measured by a chemiluminescence meter or liquid scintillation meter. Firefly Luciferase is a commonly used bioluminescence reporter gene, which can be used as a control to study the translation efficiency of target genes in mammalian cells, Cell viability and in vivo imaging measurements. This product effectively reduces the autoimmunogenicity of mRNA in mammalian cells and enhances its stability by introducing N1-Me Pseudo UTP as a replacement for natural UTP. It also simulates mature mRNA with a 5 &#8216;Cap 1 structure and a 3&#8217; poly (A) tail, making it an ideal choice for studying transfection and expression using various assays</p>



<p class="wp-block-paragraph">This product is a mature mRNA with a 5 &#8216;Cap 1 structure and a 3&#8217; poly (A) tail, synthesized using the T7 High Yield RNA Transcription Kit and modified by the Cap 1 Capping System</p>



<figure class="wp-block-image size-large"><img fetchpriority="high" decoding="async" width="1024" height="216" src="https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb-1024x216.jpg" alt="" class="wp-image-4652" srcset="https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb-1024x216.jpg 1024w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb-300x63.jpg 300w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb-768x162.jpg 768w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb-260x55.jpg 260w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb-50x11.jpg 50w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb-150x32.jpg 150w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050804-Firefly-Luciferase-mRNA-N1-Me-Pseudo-UTP-28kb.jpg 1240w" sizes="(max-width:767px) 480px, (max-width:1024px) 100vw, 1024px" /><figcaption class="wp-element-caption">Legend: Firefly Luciferase mRNA (N1-Me Pseudo UTP) structure, mRNA length 2197nt, all UTPs replaced with N1-Me Pseudo UTP</figcaption></figure>



<p class="wp-block-paragraph"><strong>Product Features</strong></p>



<p class="wp-block-paragraph">1. The Cap 1 structure is more suitable for mammalian systems than the Cap 0 structure (ARCA and m7Cap) and has higher translation efficiency. Replacing UTP with modified base N1-Me-Pseudo UTP can reduce the intrinsic immune stimulation of IVT mRNA and enhance protein translation. The addition of Poly (A) tail inhibits RNA mediated innate immune activation, increasing the stability and lifespan of mRNA in vivo and in vitro. Poly (A) also plays an important role in improving translation initiation efficiency</p>



<p class="wp-block-paragraph">2. The experimental method is simple and fast, with stable results and good reproducibility</p>



<p class="wp-block-paragraph">3. mRNA is directly expressed in the cytoplasm and transfection efficiency is stable</p>



<p class="wp-block-paragraph"><strong>Product Application</strong></p>



<p class="wp-block-paragraph">1. As a reporting material for gene regulation and functional research</p>



<p class="wp-block-paragraph">2. Suitable for detecting mRNA transmission, translation efficiency, cell viability, and in vivo imaging</p>



<p class="wp-block-paragraph"><strong>Quality Control</strong></p>



<p class="wp-block-paragraph">No RNA enzyme residue, single mRNA electrophoresis band, and stable transfection efficiency</p>



<p class="wp-block-paragraph"><strong>Storage Condition</strong></p>



<p class="wp-block-paragraph">Store at -20 ℃ with RNase Free Water as the storage buffer</p>



<p class="wp-block-paragraph"><strong>Packing Size</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td>component</td><td>M050804-100</td><td>M050804-1000</td></tr><tr><td>Firefly Luciferase mRNA (N1-Me-Pseudo UTP) (1mg/ml)</td><td>100ug</td><td>1mg</td></tr></tbody></table></figure>
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			</item>
		<item>
		<title>eGFP mRNA (N1-Me-Pseudo UTP)</title>
		<link>https://www.tinzyme.com/commercial-mrna/egfp-mrna-n1-me-pseudo-utp/</link>
		
		<dc:creator><![CDATA[tinzyme]]></dc:creator>
		<pubDate>Mon, 08 May 2023 08:10:21 +0000</pubDate>
				<category><![CDATA[Commercial mRNA]]></category>
		<category><![CDATA[eGFP]]></category>
		<category><![CDATA[Solution]]></category>
		<category><![CDATA[UTP]]></category>
		<guid isPermaLink="false">https://www.tinzyme.com/?p=4647</guid>

					<description><![CDATA[M050803 eGFP mRNA (N1-Me-Pseudo UTP) Commercial mR...]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph"><strong>M050803 eGFP mRNA (N1-Me-Pseudo UTP)</strong></p>



<p class="wp-block-paragraph"><strong>Product Description</strong></p>



<p class="wp-block-paragraph">EGFP mRNA (N1 Me Pseudo UTP) encodes a green fluorescent protein, whose maximum excitation/emission light wavelengths are 488nm/509nm respectively. Transfected cells can express enhanced green fluorescence, which can be used as a control to study the transfection and expression of target genes in mammalian cells. This product can effectively reduce the autoimmunity of mRNA in mammalian cells by introducing N1 Me Pseudo UTP to replace natural UTP, Enhance the stability of mRNA while also simulating mature mRNA with a 5 &#8216;Cap 1 structure and a 3&#8217; poly (A) tail, making it an ideal choice for studying transfection and expression using various assays</p>



<p class="wp-block-paragraph">This product is a mature mRNA with a 5 &#8216;Cap 1 structure and a 3&#8217; poly (A) tail, synthesized using the T7 High Yield RNA Transcription Kit and modified by the Cap 1 Capping System</p>



<figure class="wp-block-image size-large"><img decoding="async" width="1024" height="205" src="https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb-1024x205.png" alt="" class="wp-image-4648" srcset="https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb-1024x205.png 1024w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb-300x60.png 300w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb-768x154.png 768w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb-260x52.png 260w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb-50x10.png 50w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb-150x30.png 150w, https://www.tinzyme.com/wp-content/uploads/2023/05/image-M050803-eGFP-mRNA-N1-Me-Pseudo-UTP-15kb.png 1536w" sizes="(max-width:767px) 480px, (max-width:1024px) 100vw, 1024px" /><figcaption class="wp-element-caption">Legend: eGFP mRNA (N1-Me Pseudo UTP) structure, all UTPs replaced with N1-Me Pseudo UTP</figcaption></figure>



<p class="wp-block-paragraph"><strong>Product Features</strong></p>



<p class="wp-block-paragraph">1. The Cap 1 structure is more suitable for mammalian systems than the Cap 0 structure (ARCA and m7Cap) and has higher translation efficiency. Replacing UTP with modified base N1-Me-Pseudo UTP can reduce the intrinsic immune stimulation of IVT mRNA and enhance protein translation. The addition of Poly (A) tail inhibits RNA mediated innate immune activation, increasing the stability and lifespan of mRNA in vivo and in vitro. Poly (A) also plays an important role in improving translation initiation efficiency</p>



<p class="wp-block-paragraph">2. The experimental method is simple and fast, with stable results and good reproducibility</p>



<p class="wp-block-paragraph">3. mRNA is directly expressed in the cytoplasm and transfection efficiency is stable</p>



<p class="wp-block-paragraph"><strong>Product Application</strong></p>



<p class="wp-block-paragraph">1. As a reporting material for gene regulation and functional research</p>



<p class="wp-block-paragraph">2. Suitable for detecting mRNA transmission, translation efficiency, cell viability, and in vivo imaging</p>



<p class="wp-block-paragraph"><strong>Quality Control</strong></p>



<p class="wp-block-paragraph">No RNA enzyme residue, single mRNA electrophoresis band, and stable transfection efficiency</p>



<p class="wp-block-paragraph"><strong>Storage Condition</strong></p>



<p class="wp-block-paragraph">Store at -20 ℃</p>



<p class="wp-block-paragraph"><strong>Product packaging</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td>component</td><td>M050803-100</td><td>M050803-1000</td></tr><tr><td>eGFP mRNA (N1-Me-Pseudo UTP) (1mg/ml)</td><td>100ug</td><td>1mg</td></tr></tbody></table></figure>
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			</item>
		<item>
		<title>Pseudo UTP 100mM</title>
		<link>https://www.tinzyme.com/mrna-material/pseudo-utp-100mm/</link>
		
		<dc:creator><![CDATA[tinzyme]]></dc:creator>
		<pubDate>Tue, 14 Jun 2022 10:35:40 +0000</pubDate>
				<category><![CDATA[mRNA Material]]></category>
		<category><![CDATA[M062003]]></category>
		<category><![CDATA[Pseudo]]></category>
		<category><![CDATA[Solution]]></category>
		<category><![CDATA[UTP]]></category>
		<guid isPermaLink="false">https://www.tinzyme.com/?p=3535</guid>

					<description><![CDATA[M062003-Pseudo UTP 100mM
Pseudo UTP 100mM is a 100...]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph"><a href="https://www.tinzyme.com/man/M062003.pdf" data-type="link" data-id="https://www.tinzyme.com/man/M062003.pdf" target="_blank" rel="noreferrer noopener">Manual</a></p>



<p class="wp-block-paragraph"><strong>Product Number: M062003</strong></p>



<p class="wp-block-paragraph"><strong>Description</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td>Product Name</td><td>Pseudo UTP 100mM</td></tr><tr><td>CAS Number</td><td>1175-34-4 (Free acid)</td></tr><tr><td>Molecular Weight</td><td>550.1</td></tr><tr><td>Molecular Formula</td><td>C9H12N2Na3O15P3</td></tr><tr><td>Storage Condition</td><td>-20°C</td></tr><tr><td>Source</td><td>Chemical synthesis</td></tr></tbody></table></figure>



<p class="wp-block-paragraph"><strong>Specification</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td>Test</td><td>Specification</td></tr><tr><td>Appearance</td><td>Clear colorless solution</td></tr><tr><td>λmax</td><td>262nm±2nm</td></tr><tr><td>pH(22~25°C)</td><td>7.0±0.1</td></tr><tr><td>Bioburden</td><td>≤1cfu/ml</td></tr><tr><td>Endotoxin</td><td>&lt;1EU/ml</td></tr><tr><td>Purity (HPLC)</td><td>≥97%</td></tr><tr><td>DNase Testing</td><td>None detectable</td></tr><tr><td>RNase Testing</td><td>None detectable</td></tr><tr><td>Concentration</td><td>100mM±3%</td></tr><tr><td>Transcription reaction</td><td>Suitable</td></tr></tbody></table></figure>



<p class="wp-block-paragraph"><strong>Order</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td>M062003</td><td>Pseudo UTP 100mM</td><td>Purity (HPLC) 97%</td></tr></tbody></table></figure>
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			</item>
		<item>
		<title>N1-Me-Pseudo UTP 100mM Solution</title>
		<link>https://www.tinzyme.com/nucleotides/n1-me-pseudo-utp-100mm-solution/</link>
		
		<dc:creator><![CDATA[tinzyme]]></dc:creator>
		<pubDate>Fri, 24 Dec 2021 09:02:27 +0000</pubDate>
				<category><![CDATA[mRNA Material]]></category>
		<category><![CDATA[Nucleotides]]></category>
		<category><![CDATA[Pseudo]]></category>
		<category><![CDATA[Solution]]></category>
		<category><![CDATA[UTP]]></category>
		<guid isPermaLink="false">https://www.pcrmix.com/?p=3211</guid>

					<description><![CDATA[N5331, N1 methyl Pseudo UTP 100mM solution, Purity...]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph"><strong>Description</strong></p>



<p class="wp-block-paragraph">N1-methyl-pseudouridine (1-Methylpseudouridine), a methylpseudouridine, outperforms 5 mC and 5 mC/N1-methyl-pseudouridine in translation. N1-methyl-pseudouridine in mRNA enhances translation through eIF2α-dependent and independent mechanisms by increasing ribosome density.</p>



<p class="wp-block-paragraph"><strong>Product Name</strong></p>



<p class="wp-block-paragraph">N1-Me-Pseudo-UTP, 100mM Solution</p>



<p class="wp-block-paragraph">(N1-Me-Pseudouridine-5&#8242;-Triphosphate trisodium salt solution)</p>



<p class="wp-block-paragraph"><strong>CAS No.</strong></p>



<p class="wp-block-paragraph">1428903-59-6</p>



<p class="wp-block-paragraph"><strong>Molecular Formula</strong></p>



<p class="wp-block-paragraph">C<sub>10</sub>H<sub>14</sub>N<sub>2</sub>Na<sub>3</sub>O<sub>15</sub>P<sub>3</sub></p>



<p class="wp-block-paragraph"><strong>Molecular Weight</strong></p>



<p class="wp-block-paragraph">564.11</p>



<p class="wp-block-paragraph"><strong>Molar absorptivity</strong></p>



<p class="wp-block-paragraph">8500 (λ=271nm)</p>



<p class="wp-block-paragraph"><strong>Specification</strong></p>



<figure class="wp-block-table is-style-regular"><table><tbody><tr><td>Appearance</td><td>Clear colorless solution</td></tr><tr><td>Purity(by HPLC)</td><td>≥99.0%</td></tr><tr><td>λmax</td><td>272nm±2nm</td></tr><tr><td>Concentration</td><td>100mM±3</td></tr><tr><td>31P NMR(D2O)</td><td>To conform structure</td></tr><tr><td>1H NMR(D2O)</td><td>To conform structure</td></tr><tr><td>pH(in buffer solution)</td><td>7.0±0.1</td></tr></tbody></table></figure>



<p class="wp-block-paragraph"><strong>Storage Recommendation</strong></p>



<p class="wp-block-paragraph">Please store in -20°C. Always avoid freeze-thaw cycles or exposure to frequent temperature changes. These fluctuations can greatly alter product stability.</p>



<p class="wp-block-paragraph"><strong>Quality Control</strong></p>



<p class="wp-block-paragraph">1. The concentration is verified by Uv-vis spectrophotometry.</p>



<p class="wp-block-paragraph">2. This lot of N1-Me-Pseudo-UTP is free of DNase and RNase contamination.</p>



<p class="wp-block-paragraph">3. The purity of this preparation is determined by HPLC.</p>



<p class="wp-block-paragraph"><strong>Order</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td>N5331</td><td>N1 methyl Pseudo UTP 100mM solution</td><td>100mM N1 methyl Pseudo UTP, Purity&gt;99% (HPLC), suitable for mRNA modification</td></tr></tbody></table></figure>
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			</item>
		<item>
		<title>UTP 100mM solution</title>
		<link>https://www.tinzyme.com/nucleotides/utp-100mm-solution/</link>
		
		<dc:creator><![CDATA[tinzyme]]></dc:creator>
		<pubDate>Tue, 21 Dec 2021 01:15:39 +0000</pubDate>
				<category><![CDATA[mRNA Material]]></category>
		<category><![CDATA[Nucleotides]]></category>
		<category><![CDATA[Solution]]></category>
		<category><![CDATA[UTP]]></category>
		<guid isPermaLink="false">https://www.pcrmix.com/?p=2897</guid>

					<description><![CDATA[R5331, UTP 100mM solutions, 100mM, Purity>99% (HPL...]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph">UTP 100mM solution, rUTP 100mM solution Ultra pure</p>



<p class="wp-block-paragraph"><strong>Description</strong></p>



<ul class="wp-block-list"><li>Product Name: Uridine 5&#8242;-triphosphate, sodium salt solution</li><li>Molecular Formula: C<sub>9</sub>H<sub>12</sub>N<sub>2</sub>Na<sub>3</sub>O<sub>15</sub>P<sub>3</sub></li><li>CAS Number: 19817-92-6 (free acid)</li><li>Molecular Weight: 550.09 (free acid)</li><li>Appearance: Clear Colorless solution</li><li>Concentration: 100mM±5%</li><li>Purity(HPLC): ≥99%</li><li>λmax: 262 nm±2 nm</li><li>pH: 7.0±0.1</li></ul>



<p class="wp-block-paragraph"><strong>Applications</strong></p>



<p class="wp-block-paragraph">in vitro transcription. RNA amplification. siRNA synthesis. aRNA synthesis.</p>



<p class="wp-block-paragraph"><strong>Quality Control Molecular Biology Grade</strong></p>



<p class="wp-block-paragraph">This lot of UTP has been performance tested in transcription reaction.<br>This preparation is free of DNase and RNase contamination as determined by incubation of the UTP with radioactive substrates.</p>



<p class="wp-block-paragraph"><strong>Storage Recommendations</strong></p>



<ul class="wp-block-list"><li>Long term (Infrequent use; 1-2 times per month): -70°C</li><li>Daily/Weekly use: -20°C</li><li>Always avoid freeze-thaw cycles or exposure to frequent temperature changes.</li><li>These fluctuations can greatly alter product stability.</li><li>The performance of this product is guaranteed for twelve months from the date of purchase.</li></ul>



<p class="wp-block-paragraph">rUTP solution is one component of 100mM rNTP set solution.<br>The rNTP set is a convenient set of 100 mM solutions of each ATP, CTP, GTP and UTP.</p>



<p class="wp-block-paragraph">MOQ: 1ml of each<br>Delivery time: 2-3 working days after receive the payment.<br>Payment method: T/T or western Union or Money Gram full in advance.<br>OEM and Bulk both are available</p>



<p class="wp-block-paragraph"><strong>Feature of the NTP</strong></p>



<p class="wp-block-paragraph">Greater than 99% purity confirmed by HPLC. Functionally tested in in vitro transcription. Highly stable &#8211; the neutral pH of nucleotide solutions ansures the stability during longterm storage.</p>



<p class="wp-block-paragraph"><strong>Package</strong> <strong>&amp; Delivery</strong></p>



<p class="wp-block-paragraph">Package Details:<br>1ml/ vial, 10ml/vial, 25ml 50ml 100ml 500ml, 1000ml and more</p>



<p class="wp-block-paragraph">Delivery Time:<br>3 working days</p>



<p class="wp-block-paragraph"><strong>Order</strong></p>



<figure class="wp-block-table"><table><tbody><tr><td>R5331</td><td>UTP 100mM solutions</td><td>100mM, Purity&gt;99% (HPLC), for RNA synthesis, GMP grade available</td></tr></tbody></table></figure>
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