Collibri™ Library Amplification Master Mix with Primer Mix
Collibri™ Library Amplification Master Mix with Primer Mix
Invitrogen™

Collibri™ Library Amplification Master Mix with Primer Mix

Invitrogen Collibri Library Amplification Master Mix is a ready-to-use solution designed for amplification of next-generation sequencing (NGS) libraries. The master자세히 알아보기
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카탈로그 번호반응 수
A3854005050
A38540250250
카탈로그 번호 A38540050
제품 가격(KRW)
216,000
線上優惠
Ends: 31-Dec-2025
253,000
할인액 37,000 (15%)
Each
카트에 추가하기
반응 수:
50
제품 가격(KRW)
216,000
線上優惠
Ends: 31-Dec-2025
253,000
할인액 37,000 (15%)
Each
카트에 추가하기
Invitrogen Collibri Library Amplification Master Mix is a ready-to-use solution designed for amplification of next-generation sequencing (NGS) libraries. The master mix includes Platinum SuperFi DNA Polymerase in combination with a proprietary reaction buffer containing all necessary components for efficient library amplification with minimal bias and superior accuracy.

Feature include:
High fidelity—minimal error rates similar to PCR-free methods
High efficiency—high yields from minute input amounts
Minimal bias—uniform amplification regardless of GC content

This Collibri Library Amplification Master Mix is supplied with a 10X Primer Mix that targets the P5 and P7 regions of Illumina adapters. The master mix is supplemented with an inert blue dye, while the primer mix contains a yellow dye. Mixing both components in a PCR reaction turns the final PCR solution green. This provides a visual aid when pipetting and helps decrease the risk of pipetting errors during reaction setup.

Platinum SuperFi DNA Polymerase has both 5’ to 3’ polymerase and 3’ to 5’ exonuclease (proofreading) activities, but lacks 5’ to 3’ exonuclease activity. Exceptionally strong proofreading activity ensures amplification of NGS libraries with supreme sequence accuracy, producing NGS error rates similar to PCR-free methods.

The proprietary reaction buffer contains all necessary PCR components and additives to enable efficient and uniform library amplification regardless of GC content, helping improve coverage across GC- and AT-rich sequences and other complex regions. High amplification efficiency enables the use of fewer cycles to achieve the desired yield.

Platinum hot-start technology inhibits DNA polymerase activity at ambient temperatures, allowing room temperature reaction setup and storage of pre-assembled PCR reactions for up to 24 hours prior to the PCR.

For Research Use Only. Not for use in diagnostic procedures.
사양
Fidelity (Taq 대비)≥100
용도(애플리케이션)Sequencing
형태Liquid
GC-Rich PCR 성능High
핫 스타트Built-In Hot Start
반응 수50
오버행Blunt
제품라인Collibri
제품 유형Library Amplification Master Mix
수량50 reactions
반응 형식SuperMix or Master Mix
샘플 종류DNA, RNA
배송 조건Dry Ice
테스트 시간Standard
Unit SizeEach
구성 및 보관
• 1 x 1.25 mL Collibri Library Amplification Master Mix (2X)
• 1 x 500 µL Primer Mix

Store at -20°C.

자주 묻는 질문(FAQ)

Are PCR products generated using the Collibri Library Amplification Master Mix blunt-ended?

Yes, PCR products generated using the Collibri Library Amplification Master Mix are blunt-ended.

Is Collibri Library Amplification Master Mix compatible with magnetic beads?

Yes, Collibri Library Amplification Master Mix is compatible with magnetic beads provided in Collibri library preparation kits and in Agencourt AmPure XP system from Beckman Coulter.

What is the fidelity of the Collibri Library Amplification Master Mix?

The Collibri Library Amplification Master Mix contains Platinum SuperFi DNA Polymerase that has strong 3' to 5' exonuclease (proofreading) activity for superior amplification accuracy, greater than 100-fold in comparison with Taq polymerase.

What are the recommended storage conditions for the Collibri Library Amplification Master Mix?

We recommend storing the Collibri Library Amplification Master Mix at -20 degrees C.

Is Collibri Library Amplification Master Mix suitable for amplification of libraries prepared from FFPE samples?

Yes, however, additional PCR cycles (1-3) are typically needed with FFPE DNA or other challenging samples. To determine the optimal PCR conditions, use the table in the user manual (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0017582_Platinum_SuperFi_LibraryAmp_MM_w_Primer_Mix_UG.pdf) with the required number of PCR cycles per sample size as a starting point.

인용 및 참조 문헌 (1)

인용 및 참조 문헌
Abstract
High-resolution microbiome analysis enabled by linking of 16S rRNA gene sequences with adjacent genomic contexts.
Authors:Kapustina Ž, Medžiune J, Alzbutas G, Rokaitis I, Matjošaitis K, Mackevicius G, Žeimyte S, Karpus L, Lubys A
Journal:Microb Genom
PubMed ID:34473015
Sequence-based characterization of bacterial communities has long been a hostage of limitations of both 16S rRNA gene and whole metagenome sequencing. Neither approach is universally applicable, and the main efforts to resolve constraints have been devoted to improvement of computational prediction tools. Here, we present semi-targeted 16S rRNA sequencing (st16S-seq), ... More