GeneCopoeia All-in-OneTM Q-PCR Primer Array User Manual

All-in-OneTM Q-PCR Primer Array User's Manual is a product manual published by GeneCopoeia Inc. It mainly introduces the use of the product, precautions, product form and other information


GeneCopoeia All-in-OneTM Q-PCR Primer Array User Manual - cover page
Brand
GeneCopoeia
Category
Other
Document type
User Manual
Language
Chinese
Pages
7
File format
PDF
File size
478 KB
Published
23 December, 2011
Updated
01 October, 2023
MD5 checksum
A8FEB95ED394A4FBE036E2C51C55628B

About this manual

The All-in-OneTM Q‑PCR Primer Array is a ready‑to‑use 96‑well plate containing 96 optimized primer pairs, including four internal reference genes. It enables rapid, quantitative gene‑expression profiling using Real‑Time PCR with SYBR Green detection.

The manual provides product overview, storage and handling precautions, detailed experimental procedures (RNA preparation, cDNA synthesis, qPCR setup, and data analysis), instrument compatibility, and troubleshooting tips. An appendix describes the ΔΔCt data‑analysis method and includes a specific Wnt‑signaling panel example. This manual is written in Chinese.

What's inside

  • Product Overview
  • Product Advantages
  • Usage Precautions
  • Product Formats & Instrument Compatibility
  • Detailed Experimental Procedure
  • RNA Sample Preparation
  • cDNA Preparation
  • qPCR Reaction Setup
  • Data Analysis
  • FAQ & Troubleshooting

Specifications

Number of primer pairs96
Internal reference genes4 primer pairs
Storage temperature+2 °C ~ +8 °C
Ready‑to‑Use formatAdd Q‑PCR Mix, cDNA and water only
Instrument compatibilityFour packaging formats for major Real‑Time PCR instruments

Frequently asked questions

Why does the All-in-OneTM Q‑PCR Primer Array not include a genomic DNA contamination detection?

Over 95 % of the primers are designed across introns, which prevents amplification of genomic DNA, so a separate contamination control is unnecessary.

Why is there no reverse‑transcription efficiency detection in the array?

Efficiency can be inferred from the Ct values of internal reference genes (e.g., GAPDH or ACTB); a Ct > 25 indicates possible problems.

What RNA purity is required for reliable results?

The RNA OD260/280 ratio should be between 1.7 and 2.0.

What RNA integrity ratio indicates non‑degraded RNA?

A 28S : 18S ratio of approximately 2 : 1 is considered acceptable.

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