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usage
sufficient for 100 reactions
feature
dNTPs included, hotstart
technique(s)
RT-PCR: suitable, cDNA synthesis: suitable
Quality Level
color
colorless
input
purified RNA
shipped in
wet ice
storage temp.
−20°C
Categorie correlate
1 of 4
Questo articolo | |||
|---|---|---|---|
| technique(s) RT-PCR: suitable | technique(s) RT-qPCR: suitable | technique(s) RT-PCR: suitable, RT-qPCR: suitable | technique(s) RT-PCR: suitable, qPCR: suitable |
| usage sufficient for 100 reactions | usage sufficient for 250 reactions | usage sufficient for 150 reactions, sufficient for 50 reactions | usage sufficient for 100 reactions, sufficient for 1000 reactions, sufficient for 500 reactions |
| feature dNTPs included | feature dNTPs included, hotstart | feature hotstart | feature dNTPs included: no, hotstart: no |
| color colorless | color colorless | color - | color - |
| input purified RNA | input purified RNA | input purified RNA | input purified DNA |
| shipped in wet ice | shipped in wet ice | shipped in - | shipped in - |
General description
One-step: In a single tube, eAMV™ RT and AccuTaq LA act sequentially to first produce cDNA and then immediately amplify by PCR. This provides quick, sensitive analysis of RNA.
Two-step: Each reaction is individually optimized for greater yields with high fidelity, when protocol requires multiple amplifications, or if maximum yield is more important than maximum convenience.
Application
Features and Benefits
- Greater transcription lengths than other reverse transcriptases, generating cDNA up to 14.1 Kb.
- Higher sensitivity for detecting low abundance messages. eAMV™ RT is able to transcribe RNA that other reverse transcriptases cannot detect.
- Unsurpassed transcription through difficult secondary structure.
- Increased sensitivity, specificity and yield from JumpStart AccuTaq LA DNA Polymerase.
Other Notes
Legal Information
Classe di stoccaggio
10 - Combustible liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
signalword
Danger
wgk
WGK 3
hcodes
Hazard Classifications
Aquatic Chronic 3 - ED ENV 1
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Articoli
Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.
Protocolli
REDAccuTaq LA protocol offers high-fidelity amplification of long PCR fragments with direct gel loading capability.
The 3’/5’ integrity assay identifies RNA degradation, crucial for large sample sets or less detectable degradation.
Contenuto correlato
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Major technological advances have made the production of monoclonal antibodies quicker and more efficient. There are three established platforms for antibody discovery. We offer reagents for production of monoclonal antibody libraries using each of these techniques.
Progressi tecnologici di grande impatto hanno reso la produzione di anticorpi monoclonali più rapida e più efficiente. Per la scoperta di anticorpi esistono ormai tre piattaforme consolidate. Proponiamo reagenti per la produzione di librerie di anticorpi monoclonali con ognuna di queste tre tecniche proponiamo
Strumenti per la preparazione dei plasmidi, la trascrizione in vitro, la purificazione dell'mRNA e la formulazione di LNP nello sviluppo di vaccini e terapie a base di mRNA.
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