Swift Accel-NGS XL试剂盒

世界*实验材料供应商 Swift Biosciences上海金畔生物为其中国代理， Swift Biosciences在一直是行业的*,一直为广大科研客户提供zui为的产品和服务,上海金畔生物一直秉承为中国科研客户带来的产品，的服务， Swift Biosciences就是为了给广大科研客户带来更加完善的产品和服务,您的满意将是我们zui大的收获

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Swift Biosciences是一家生物技术公司，正在开发新的分子生物学技术，以更好地表征和理解基因组。我们是一个精力充沛，高度创新的公司，专注于创造推动DNA测序科学的工具。我们的产品旨在帮助客户分析经常与翻译工作相关的挑战性样品，包括循环，无细胞DNA和福尔马林固定的石蜡包埋样品。

斯威夫特创新的科学家和高管团队在加入发现方面拥有强大的记录，具有开展新应用和市场功能的功能。我们的产品开发是有目的的，专注于创造客户及其目标行业受到好评的产品。斯威夫特的使命是为世界各地的个人及其社区的健康提供长期的改善，特别是在抗击癌症和了解遗传疾病的复杂性方面。我们努力开发的工具直接适用于农业，生物技术，宏基因组学和制药行业的研究。

该公司成立于2010年，由具有成功业务历史和经验丰富的生命科学投资者支持的科学家团队成立。我们不断发展壮大的科学家团队开发的创新流程为基因组学领域的翻译研究生成了多项经过验证的产品，我们期待着为我们的产品组合添加新的技术和产品。

Accel-NGS® XL Library Kit for Pacific Biosciences®

Reliable Long-Read Sequencing Solutions for Genome Assembly and Genomic Phasing

Get Better Quality Genome Assemblies. Faster.

The Swift Biosciences Accel-NGS XL Library Kit designed for the Pacific Biosciences (PacBio®) platform is the fastest sequencing solution for genome assembly and haplotype sequencing on PacBio platforms. Long-read sequencing technology provides better coverage to sequence difficult genomic regions including low complexity, repetitive elements, or large structural variation. Until now, the standard protocol has had a long workflow that reduces your productivity.

The Accel-NGS XL Library Kit for PacBio is a novel library preparation kit optimized for Pacific Biosciences’ Single Molecule, Real-Time (SMRT®) sequencing. It provides significantly longer read lengths from less sample input along with a simple workflow to accelerate your path to discovery. At the core, this library prep kit leverages Swift’s enhanced repair and ligation chemistry to produce a high library conversion rate, while simultaneously preventing adapter dimer formation and preserving DNA integrity.

This kit replaces the PacBio SMRTbell™ Template Prep Kit and works in conjunction with the PacBio DNA Polymerase Binding and MagBead loading kits. It is compatible with the PacBio RS II and Sequel™ platforms and contains sufficient material for constructing 16 sequencing libraries.

Features:

• Generates average read length up to 20 kb
• Ready-to-sequence libraries in 1 day
• Simple assay for whole genome sequencing
• Inputs as low as 2 µg

Benefits:

• Improve your genomic assembly with longer read lengths
• Double your productivity with libraries generated in a single day
• Reduce labor cost and error rates with less sample processing
• Compatible with a wider range of sample input amounts