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usage
sufficient for 100 reactions, sufficient for 25 reactions, sufficient for 500 reactions
feature
dNTPs included, hotstart: no
technique(s)
RT-PCR: suitable, cDNA synthesis: suitable
color
colorless
input
purified RNA
shipped in
dry ice
storage temp.
−20°C
Categorías relacionadas
1 of 4
Este artículo | P4600 | 11483188001 | FPCR-RO |
|---|---|---|---|
| technique(s) RT-PCR: suitable | technique(s) PCR: suitable | technique(s) RT-PCR: suitable | technique(s) PCR: suitable |
| usage sufficient for 100 reactions | usage sufficient for 100 reactions | usage sufficient for 30 reactions (including 5 control reactions) | usage sufficient for ≤2,000 reactions (04710452001), sufficient for ≤100 reactions (04710436001), sufficient for ≤400 reactions (04710444001) |
| feature dNTPs included | feature dNTPs included, hotstart: no | feature dNTPs included, hotstart: no | feature - |
| color colorless | color colorless | color - | color - |
| input purified RNA | input purified DNA | input purified RNA | input - |
| shipped in dry ice | shipped in wet ice | shipped in - | shipped in - |
General description
Application
Features and Benefits
- Convenient 5X master mix formula provides for quick and easy reaction set up; just add RNA template
- Includes proprietary blend of randomers and oligodT primers and an RNAse H+ derivative of Moloney murine leukemia virus (MMLV) reverse transcriptase
- Allows for unbiased, accurate conversion of RNA to cDNA in just 40 minutes
- Can use up to 1 μg of RNA in a single 20 μL reaction; reactions can also be scaled up
- Highly stable; can be stored at -20°C for up to 1 year; 4°C for up to one month
- Specific ratio of randomers and oligo (dT) primers in the mastermix ensures optimal representation of all transcript sequences in the cDNA product
- High reproducibility: Premixed master mix eliminates variability inherent in other kits requiring mixing of components
- RNase H(+) Moloney murine leukemia virus (MMLV) reverse transcriptase ensures residual RNA does not interfere with PCR amplification
- Reverse transcribes both rare and abundant genes with a wide input range of template
- Convenient 5X master mix formula provides for quick and easy reaction set up; just add RNA template
Other Notes
Legal Information
related product
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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Artículos
Sigma’s Imprint RNA Immunoprecipitation Kit was used to copurify human argonaute 2 (Ago2)-associated RNAs from HeLa cells. MicroRNAs reverse transcribed and quantitating using Mysticq reagents.
Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.
Protocolos
Method for reverse transcription of RNA into DNA. Uses a premixed reagent that contains reverse transcriptase, dNTPs, primers, RNase inhibitor and buffer. Fast generation of cDNA.
Reverse transcription analyzes mRNA gene expression, facing challenges like transcript half-life differences and temporal patterns.
Notre protocole de qPCR avec SYBR Green est conçu pour quantifier précisément l'expression génique ou des réactions de RT-PCR.
Contenido relacionado
Polymerase chain reaction (PCR) is a technique for amplifying nucleic acid molecules and is commonly used in many applications, including RT-PCR, hot start PCR, end point PCR and more.
La reacción en cadena de la polimerasa (PCR) es una técnica de amplificación de moléculas de ácidos nucleicos y se utiliza habitualmente en muchas aplicaciones, entre ellas la RT-PCR (retroPCR), la PCR de inicio en caliente, la PCR de punto final.
La réaction en chaîne par polymérase (PCR pour "Polymerase Chain Reaction") est une technique d'amplification des molécules d'acide nucléique qui est couramment employée dans de nombreuses applications, incluant la RT-PCR, la PCR à démarrage à chaud, la PCR en point final, et bien d'autres.
RT-qPCR detects specific targets with applications in gene expression and pathogen detection.
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