VAHTS Universal Plus DNA Library Prep Kit for Illumina
VAHTS ® Universal Plus DNA Library Prep Kit for Illumina is a DNA library construction kit developed for the Illumina ® high-throughput sequencing platform.
The supplier does not provide quotations for this product through SelectScience. You can search for similar products in our Product Directory.
Great results with good buffer
analyzer for RNA samples
VAHTS universal V8 RNA-seq library prep kit for illumina is specially designed for the preparation of transcriptome libraries for illumina platform. The kit is universal and suitable for RNA library construction of RNA that have been obtained by poly(A)-based mRNA enrichment or RNA depletion, the kit contains two types of cDNA 2nd strand synthesis buffer, which can be chosen for library construction for non-stranded or stranded RNA-seq transcriptome analysis.
Review Date: 26 May 2022 | Vazyme Biotech Co., Ltd
VAHTS® Universal Plus DNA Library Prep Kit for Illumina is a DNA library construction kit developed for the Illumina® high-throughput sequencing platform. This kit combines DNA fragmentation, end repair, and dA tailing into one step. The product does not need to be purified. It is directly connected to adapters, library enrichment and sorting, and can convert 100 pg-1 μg template DNA into Illumina® Qualcomm Volume sequencing platform dedicated library. There is no need to mechanically interrupt the genome, which simplifies the library construction process and shortens the operation time, and is suitable for PCR and PCR-Free library construction. This kit is perfectly compatible with different sources and different input amounts of DNA, and only needs to adjust the fragmentation time according to the target insert size to obtain the desired fragment size library.
Product Advantages
- Wide compatibility: easy to deal with different species sources, different initial inputs and different template types
- Simple operation: just adjust the fragmentation time according to the target insert fragment size to get the required library
- High library yield: excellent library conversion rate and better sample quality
Applications
Applicable to DNA library preparation for NGS on Illumina® platforms and compatible with 100 pg - 1 μg of input DNA and various kinds of DNA template including genomic DNA (from different species such as animals, plants, and microorganisms), paraffin sections DNA (FFPE DNA), etc.
It is recommended to use this kit for:
- Whole genome sequencing
- Whole exome or targeted sequencing (using IDT xGen™ Lockdown™ Probes, Roche® NimbleGen™ SeqCap™ EZ or other hybridization capture systems).
- Metagenome sequencing.
- Methylation Sequencing (in combination with Phanta UC Super-Fidelity DNA Polymerase for Library Amplification, Vazyme #P507).
Notes:
The parameters of library preparation procedures may be adjusted according to sample types, experimental designs, instruments, and operations. For any questions during procedures, please contact Vazyme for help at global@vazyme.com.
Single Cell WGA/WTA Library Prep Solution Discover-sc Single Cell WGA Kit (N603)
In this application note, Vazyme Biotech introduces the Discover-sc® Single Cell WGA Kit, which is designed for unbiased whole genome amplification from single cell and other micro samples.
Identifying novel aging genes and investigating their pathological role in breast cancer
The lifespan of mouse-inbred strains varies dramatically, indicating the genetic regulation of aging. To reveal the genetic mechanisms of aging, Dr. Rong Yuan and his team measured the lifespan of 32 inbred strains and longitudinally investigated the development and aging related phenotypes. The results suggest that the age of vaginal patency (AVP), a bio-marker of female sexual maturation (FSM), and the circulating IGF1 level, can be used as bio-markers of aging. By quantitative trait loci (QTL) analysis, combining bioinformatic methods, a group of novel aging related genes were identified, including nuclear receptor interacting protein 1 (NRIP1). Pathologic studies revealed that NRIP1 deletion could suppress the initiation and progress of breast cancer. Next-generation sequencing and single-cell RNA sequencing could significantly improve the ability to identify QTL genes and discover the molecular mechanisms of cancer.
In this webinar, join Dr. Rong Yuan and Shuyun Ding as they share how to identify novel aging-related genes and their pathological role in cancer. Plus, discover how to improve your research by using singe cell RNA sequencing and next-generation sequencing (NGS), and explore detailed applications for single-cell RNA sequencing.
Key learning objectives
- Discover how to identify novel aging-related genes and their pathological role in cancer
- Explore the principles and applications of next-generation sequencing
- Learn more about detailed applications for single-cell RNA sequencing
Who should attend?
- Scientists and clinicians with experience in NGS, biology, and genomics
Certificate of attendance
All webinar participants can request a certificate of attendance, including a learning outcomes summary, for continuing education purposes.
