Toyobo QPS-101T Probe qPCR Mix Instruction Manual

The Toyobo QPS-101T Probe qPCR Mix instruction manual provides components, protocol, cycling conditions, and troubleshooting for real‑time PCR using TaqMan…


Toyobo QPS-101T Probe qPCR Mix Instruction Manual - cover page
Brand
TOYOBO
Document type
User Manual
Language
English
Pages
14
File format
PDF
File size
169 KB
Published
03 October, 2026
Updated
03 October, 2026
MD5 checksum
5C67EE11C363275564F331742E28AEBD

About this manual

The THUNDERBIRD™ Probe qPCR Mix is a 2× master mix designed for real‑time PCR with TaqMan® probes. It contains all required reagents except the ROX reference dye, which is supplied separately, and includes hot‑start antibodies for improved specificity and efficiency. The kit is intended for research use only and is compatible with most block‑type and glass‑capillary real‑time cyclers.

The manual covers the product components, guidelines for primer and probe design, template DNA options, detailed reaction setup, recommended thermal cycling parameters for various instruments, related cDNA synthesis protocols, troubleshooting tips, and a list of related products and licensing information.

What's inside

  • Introduction
  • Components
  • Primer/Probe design
  • Template DNA
  • Protocol
  • Related Protocol
  • Troubleshooting
  • Related products
  • License notice

Specifications

Storage temperature (long term)-20°C, protected from light
Kit volume1 mL per kit (QPS-101T)
ROX reference dye50× ROX reference dye supplied separately
Hot‑start technologyAnti‑Taq DNA polymerase antibodies
Cycler compatibilityWorks with most block‑type and glass‑capillary real‑time cyclers

Frequently asked questions

How should the THUNDERBIRD Probe qPCR Mix be stored?

Store the mix at –20 °C, protected from light for long‑term storage, or at 2‑8 °C for up to three months for short‑term use.

What can cause loss of linearity at high cDNA/DNA concentrations?

Inhibition by components in the cDNA/DNA solution, such as PCR inhibitors in the DNA sample, can cause loss of linearity; repurifying the DNA often resolves the issue.

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