No, libraries made with SeqPlex™-I WTA Kit fit directly into NGS workflows. Sequencing instrument operators should be notified of running libraries created with SeqPlex™-I WTA Kit and to expect a slight signal from any remaining primers in the IVC plots.
SEQRI
SEQPLEX-I WTA Kit
Whole Transcriptome Amplification, RNA Amplification
Sinonimo/i:
RNA amplification kit
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CHF 1’190.00
Spedizione prevista il14 aprile 2025
Scegli un formato
About This Item
CHF 1’190.00
Spedizione prevista il14 aprile 2025
Prodotti consigliati
tecniche
whole genome amplification: suitable
whole transcriptome amplification: suitable
Compatibilità
Illumina (Next Generationa Sequencing)
Condizioni di spedizione
wet ice
Temperatura di conservazione
−20°C
Descrizione generale
Pre-amplification/Library Synthesis: In the Pre-amplification/Library Synthesis step using the (Library Preparation Reagents), the template RNA is reverse transcribed using primers composed of a semi-degenerate 3′- and universal 5′-ends. As polymerization proceeds, displaced and RNaseH generated single strands serve as new templates for additional primer annealing and extension producing random, overlapping cDNAs flanked by a universal primer (5′) and primer complement (3′) sequence.
Amplification 1: In the Amplified Library Synthesis step (using the Amplification 1 Reagents), products from pre-amplification/library synthesis are amplified by single primer PCR via the proprietary universal end sequence. These amplification products typically range from 200 to 500+ base pairs. Note: Amplicons from degraded RNA, such as Formalin Fixed Paraffin Embedded (FFPE), are typically shorter and dependent upon the length of the starting RNA.
Amplification 2: In the Sequencing Library Synthesis step (using Amplification 2 Reagents), single primer amplicons from amplification 1 are converted to dual Illumina® primer PCR products ready for purification, quantification, and Illumina® NGS.
Applicazioni
Caratteristiche e vantaggi
- Amplifies fragmented/extremely small quantities of total RNA: Fragmented or intact RNA from all sources including FFPE and RIP are easily amplified by random priming technology.
- Semi-degenerate library primer design ensures more complete transcriptome coverage and efficient priming
- Fewer Steps: No need to fragment cDNA before sequencing
- High-efficiency: Amplifies ds-cDNA in 8 hours or less
- Cost-effective: No longer requires an additional NGS library prep step
- Compatible with Illumina® next generation sequencing
Altre note
a) The reagents in this kit have been tested to assure that RNases are absent.
b) The user, however, must protect the integrity of experimental results by wearing basic protective equipment, including gloved hands and lab coat.
c) All reagent transfers throughout this procedure should be performed in a laminar flow hood or dedicated clean room.
d) Frozen RNA samples should be thawed on ice.
2) A 20 μL Amplification 2 reaction will produce >100 ng of amplified double-stranded cDNA when starting with 100 pg to 5 ng of high-quality RNA. Higher input quantities and higher quality RNA template generally result in increased yields. For damaged RNA, such as from FFPE, 1–50 ng input RNA is recommended.
3) The dual index adapter primers (AP100) provided in this kit will only work for one sample. If pooling samples for sequencing is required, the user must provide additional index primer sets. See example index primer sequences on page 2 of the technical bulletin.
Note legali
Esclusione di responsabilità
Prodotti correlati
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Resp. Sens. 1
Codice della classe di stoccaggio
10 - Combustible liquids
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Articoli
SeqPlex™-I WTA kit amplifies RNA for NGS, enabling genomic studies from limited samples.
Contenuto correlato
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
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Will SeqPlex™-I libraries require special NGS sequencing protocols?
1 answer-
Helpful?
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Are there advantages to SeqPlex™-I over GenomePlex?
1 answer-
SeqPlex™-I Pre-Amplification primers have been designed to target more frequently than existing GenomePlex WTA primers and therefore may provide the advantage of superior genome coverage in some regions.
Helpful?
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Is SeqPlex™-I WTA Kit compatible with microarrays and qPCR?
1 answer-
Yes, libraries made using SeqPlex™-I WTA Kit can be used in these applications like genomic DNA or existing GenomePlex products.
Helpful?
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Will reducing cycles during amplification improve representation?
1 answer-
No, you need to reach “plateau” for optimum representation. Proceeding past 1-2 cycles will not negate the reactions, but best representation is achieved around “plateau”. Insufficient cycling leads to a significant reduction in representation/coverage.
Helpful?
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