Skip to main content
メニュー
Revvity logo
Contact us
JP
Revvity Sites Globally

Select your location.

*e-commerce not available for this region.

australia.webp Australia
austria.webp Austria
belgium.webp Belgium
brazil.webp Brazil *
canada.webp Canada
china.webp China *
denmark.webp Denmark
finland.webp Finland
france.webp France
germany.webp Germany
hong-kong.webp Hong Kong (China) *
india.webp India *
ireland.webp Ireland
italy.webp Italy
japan.webp Japan *
luxembourg.webp Luxembourg
mexico.webp Mexico *
netherlands.webp Netherlands
norway.webp Norway
philippines.webp Philippines *
republic of korea.webp Republic of Korea *
singapore.webp Singapore *
spain.webp Spain
sweden.webp Sweden
switzerland.webp Switzerland
thailand.webp Thailand *
uk.webp United Kingdom
usa.webp United States
Breadcrumb
...
  • ホーム
  • Products
  • 研究・開発
  • ゲノム解析
  • ライブラリー調製キット
  • Small RNA Sequencing Library Prep Kits
  • miND Spike-In Controls

miND Spike-In Controls

miND Spike-In Controls
miND Spike-In Controls
miND Spike-In Controls
miND Spike-In Controls
miND Spike-In Controls

miND® Spike-In Controls are a ready-to-use mix of synthetic small RNAs added to total RNA before library prep. They have two core functions. First, they serve as a quality control that verifies the dynamic range and quantitative performance of the assay. Second, they enable absolute normalization of sequencing data, converting read counts to copies per microliter. This matters because small RNA sequencing from biofluids often varies in RNA content, making relative metrics like RPM (reads per million) potentially be misleading. By anchoring results in absolute units, miND Spike-Ins improve cross-sample and cross-batch comparability.

miND Spike-In Controls are comprised of seven oligonucleotides with unique 13 nt core sequences flanked by randomized bases, supplied in defined ratios spanning typical small-RNA abundances. They are compatible with ligation-based small RNA-seq across species and matrices, including plasma, serum, urine, CSF, synovial fluid, cells, tissues, extracellular vesicles, and non-vesicular fractions. The miND Spike-In Controls pair naturally with NEXTFLEX™ Small RNA kit as an accessory to standardize runs across studies and batches.

View product information
Feature Specification
Product Group small RNA用アクセサリー

miND® Spike-In Controls are a ready-to-use mix of synthetic small RNAs added to total RNA before library prep. They have two core functions. First, they serve as a quality control that verifies the dynamic range and quantitative performance of the assay. Second, they enable absolute normalization of sequencing data, converting read counts to copies per microliter. This matters because small RNA sequencing from biofluids often varies in RNA content, making relative metrics like RPM (reads per million) potentially be misleading. By anchoring results in absolute units, miND Spike-Ins improve cross-sample and cross-batch comparability.

miND Spike-In Controls are comprised of seven oligonucleotides with unique 13 nt core sequences flanked by randomized bases, supplied in defined ratios spanning typical small-RNA abundances. They are compatible with ligation-based small RNA-seq across species and matrices, including plasma, serum, urine, CSF, synovial fluid, cells, tissues, extracellular vesicles, and non-vesicular fractions. The miND Spike-In Controls pair naturally with NEXTFLEX™ Small RNA kit as an accessory to standardize runs across studies and batches.

View product information
Product variant
Unit Size: 96 rxns
Part #:
KT-041-MIND-96-LP
For research use only. Not for use in therapeutic or diagnostic procedures.
Request more information
miND Spike-In Controls
miND Spike-In Controls
miND Spike-In Controls
miND Spike-In Controls
miND Spike-In Controls
miND Spike-In Controls
Quick links
  • Product information
  • Resources
  • SDS, COAs, manuals and more
  • Related products
  • Get help

Product information

  • Overview
  • Specifications

Overview

miND Spike-In Controls calibrate and quality check small RNA-seq by adding defined small RNA standards to each sample before library prep. They verify the dynamic range of the assay and enable absolute
quantitation, converting reads into copies per microliter for more reliable cross-sample and cross-batch comparisons, especially in biofluids and other
low-input matrices.

  • Seven synthetic spike-ins supplied in defined ratios to span typical range of endogenous small-RNA abundances.
  • Unique 13-nt core with four randomized bases at both ends, designed to minimize ligation bias; 5′-phosphorylated.
  • Absolute quantitation via linear regression to output molecules/µL..
  • Simple integration: add 1 µL per RNA sample just before NEXTFLEX small RNA-seq library prep.
  • Broad compatibility across species and matrices including plasma, serum, urine, CSF, synovial fluid, EVs, cells, and tissues.
  • Simple format: 96 reaction lyophilized.
  • Built-in analysis support: TAmiRNA provides ready-to-use scripts and a Docker/Snakemake pipeline on GitHub to quantify miRNAs and the spike-ins, then fit a regression to report absolute unit.

Specifications

Product Group
Small RNA Accessory
Shipping Conditions
Shipped Ambient
Unit Size
96 rxns

Resources

Are you looking for resources, click on the resource type to explore further.

  • - すべて -:-:- Any -
  • Flyer:-:1
1-1 of 1 Resources
Flyer Icon
Flyer
A unique NGS workflow for absolute quantitation of microRNAs and other small RNAs in any biological sample and species

Flyer illustrating how miND Spike-Ins can be used for absolute quantitation of microRNAs and oher small RNAs in any biological...

Learn more

How can we help you?

We are here to answer your questions.

Contact sales I would like more product information Contact customer care Get technical support
Get Help Illustration Get Help Illustration
Scroll Icon
Revvity Logo

©2025 Revvity - All rights reserved

Revvity is a trademark of Revvity, Inc. All other trademarks are the property of their respective owners.