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DUO92021

Sigma-Aldrich

Duolink® In Situ PLA® Probe Anti-Human MINUS

Affinity purified Donkey anti-Human IgG (H+L)

Synonim(y):

Odczynnik do testu interakcji białko-białko, Odczynnik do testu ligacji zbliżeniowej in situ

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About This Item

Kod UNSPSC:
41105331
NACRES:
NA.41

pochodzenie biologiczne

donkey (Polyclonal)

forma przeciwciała

affinity purified immunoglobulin (secondary antibody)

linia produktu

Duolink®

reaktywność gatunkowa

human

metody

immunofluorescence: suitable
proximity ligation assay: suitable

przydatność

suitable for brightfield
suitable for fluorescence

Warunki transportu

wet ice

temp. przechowywania

2-8°C

Zastosowanie

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.

This product can be applied to both the Duolink® In Situ Fluorescence Protocol and the Duolink® In Situ Brightfield Protocol depending on the detection reagents used.

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. Other necessary reagents include a pair of PLA probes from different species (one PLUS and one MINUS), 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. HRP is also available for brightfield detection.
Specificity

PLA probe anti-Human reacts with whole molecule human IgG and the light chains of other human immunoglobulins. The PLA Probe Anti-Human Minus has minimal cross-reactivity with bovine, chicken, goat, guinea pig, Syrian hamster, horse, mouse, rabbit, rat, and sheep serum proteins. A PLUS probe of a different species must be used simultaneously with this product. See our Product Selection Guide for more information.

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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Cechy i korzyści

  • 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

Komponenty

This product is comprised of the following:
  • 5x PLA Probe Anti-Human MINUS - Donkey anti-human secondary antibody conjugated to oligonucleotide MINUS
  • 1x Blocking Solution - Reagent for blocking of the sample
  • 1x Antibody Diluent - For dilution of PLA probes and primary antibodies

See datasheet for more information.

Informacje prawne

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

Aquatic Chronic 2 - Skin Sens. 1

Kod klasy składowania

10 - Combustible liquids


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Produkty

Support information including tips and tricks, frequently asked questions, and basic troubleshooting.

Things to consider for preparation, setup and execution of the Duolink® assay protocol

Protokoły

Protocol for use of Duolink® PLA reagents for the detection of individual proteins, protein modifications, and protein-protein interactions within cell populations by flow cytometry.

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