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Merck
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DUO92102

Duolink® In Situ Orange Starter Kit Mouse/Rabbit

Synonym(s):

in situ Proximity Ligation Assay reagent, Protein Protein Interaction Assay reagent

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About This Item

NACRES:
NA.32
UNSPSC Code:
41116158
Fluorescence:
λex 554 nm; λem 576 nm (orange) (Cyanine 3; Zeiss Filter set 20)
Technique(s):
proximity ligation assay: suitable
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product line

Duolink®

technique(s)

proximity ligation assay: suitable

fluorescence

λex 554 nm; λem 576 nm (orange) (Cyanine 3; Zeiss Filter set 20)

suitability

suitable for fluorescence

storage temp.

−20°C

Application

Duolink® In Situ Orange Starter Kit Mouse/Rabbit has been used in in situ interaction assay.
Duolink®proximity ligation assay(PLA®) allows for endogenous detection of protein interactions, post translational modifications, and protein expression levels at the single molecule level in fixed cells and tissue samples.

Follow the Duolink® In Situ Fluorescence Protocol to use this product. A set of short instructionsis also available.

Visit our Duolink® PLA Resource Center for information on how to run a Duolink® experiment, applications, troubleshooting, and more.

To perform a complete Duolink® PLA in situ experiment you will need two primary antibodies (PLA, IHC, ICC or IF validated) that recognize two target epitopes.This starter kit supplies all other necessary reagents for 30 Duolink® PLA reactions, which include a pair of PLA probes (Anti-Rabbit PLUS and Anti-Mouse MINUS), orange detection reagents, wash buffers, and mounting medium.Note that the primary antibodies must come from the same species as the Duolink® PLA probes. Analysis is carried out using standard immunofluorescence assay equipment.
Specificity
The Duolink® In Situ Orange Starter Kit Mouse/Rabbit requires one primary antibody from mouse and one primary antibody from rabbit. Orange fluorescence detection reagents are often used with Cyanine 3 filter.

Application Note
Two primary antibodies raised in different species are needed. Test your primary antibodies (IgG-class, mono- or polyclonal) in a standard immunofluorescence (IF), immunohistochemistry (IHC) or immunocytochemistry (ICC) assay to determine the optimal fixation, blocking, and titer conditions. Duolink® PLA in situ reagents are suitable for use on fixed cells, cytospin cells, cells grown on slide, formalin-fixed, paraffin embedded (FFPE), or tissue (fresh or frozen). No minimum number of cells is required.

Let us do the work for you, learn more about our Custom Service Program to accelerate your Duolink® projects

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Features and Benefits

  • No overexpression or genetic manipulation required
  • High specificity (fewer false positives)
  • Single molecule sensitivity due to rolling circle amplification
  • Relative quantification possible
  • No special equipment needed
  • Quicker and simpler than FRET
  • Increased accuracy compared to co-IP
  • Publication-ready results

Legal Information

Duolink is a registered trademark of Merck KGaA, Darmstadt, Germany
PLA is a registered trademark of Merck KGaA, Darmstadt, Germany


Kit Components Also Available Separately

Product No.
Description
SDS & Pricing

  • Duolink® In Situ PLA® Probe Anti-Rabbit PLUS, Affinity purified Donkey anti-Rabbit IgG (H+L)
    SDS

  • Duolink® In Situ PLA® Probe Anti-Mouse MINUS, Affinity purified Donkey anti-Mouse IgG (H+L)
    SDS

  • Duolink® In Situ Detection Reagents Orange
    SDS

  • Duolink® In Situ Wash Buffers, Fluorescence
    SDS

  • Duolink® In Situ Mounting Medium with DAPI
    SDS

signalword

Danger

wgk

WGK 3

Hazard Classifications

Aquatic Chronic 2 - ED ENV 1 - Met. Corr. 1 - Resp. Sens. 1 - Skin Sens. 1

Storage Class

10 - Combustible liquids

Regulatory Information

低风险生物材料
常规特殊物品

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Protocols

本页详细介绍了Duolink®原位精简实验方案

This protocol describes how to perform immunofluorescent detection of proteins in cells and tissue.

This page details the Duolink® In Situ Short Protocol for fluorescence detection

Articles

本实验方案描述了Duolink® PLA试剂用于组织和细胞样品中个体蛋白质、蛋白质修饰和蛋白质相互作用的免疫荧光检测、可视化和定量。

Duolink®邻位连接技术用于研究神经元相互作用,促进神经科学研究。

包括建议和技巧、常见问题解答和基本故障排除的支持信息。

View All Articles

Related Content

利用邻位连接技术对蛋白质互作、翻译后修饰和低表达蛋白进行检测、定量和成像应用。

Applications to detect, quantify and visualize protein-protein interactions, post-translational modifications and low expression protein detection using proximity ligation assay


Interactome analysis reveals ZNF804A, a schizophrenia risk gene, as a novel component of protein translational machinery critical for embryonic neurodevelopment
Zhou Y, et al.
Molecular Psychiatry (2017)
Tomokazu Sumida et al.
Nature immunology (2018-10-31)
Foxp3+ regulatory T cells (Treg cells) are the central component of peripheral immune tolerance. Whereas a dysregulated Treg cytokine signature has been observed in autoimmune diseases, the regulatory mechanisms underlying pro- and anti-inflammatory cytokine production are elusive. Here, we identify
Roberto Di Maio et al.
Science translational medicine, 10(451) (2018-07-27)
Missense mutations in leucine-rich repeat kinase 2 (LRRK2) cause familial Parkinson's disease (PD). However, a potential role of wild-type LRRK2 in idiopathic PD (iPD) remains unclear. Here, we developed proximity ligation assays to assess Ser1292 phosphorylation of LRRK2 and, separately



Global Trade Item Number

SKUGTIN
DUO92102-1KT04061833592205