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AlphaLISA Anti-Mouse IgG2b (isotyping) Acceptor Beads, 250µg

AlphaLISA™ Acceptor beads conjugated to a anti-mouse IgG2b. This bead can be used to create no-wash AlphaLISA assays for isotyping and other applications.

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Feature Specification
Application Protein-Protein Interaction

AlphaLISA™ Acceptor beads conjugated to a anti-mouse IgG2b. This bead can be used to create no-wash AlphaLISA assays for isotyping and other applications.

Click to copy promo code to clipboard.
March lab savings - SAVE 10%. Use promo code below.
MARCH10
Product Variants
Unit Size: 250 µg
Part #:
AL181C
List Price
USD 890.00
Your online price:
Unit Size: 5 mg
Part #:
AL181M
List Price
USD 8,812.00
Your online price:
Unit Size: 25 mg
Part #:
AL181R
List Price
USD 36,300.00
Your online price:
For research use only. Not for use in diagnostic procedures. All products to be used in accordance with applicable laws and regulations including without limitation, consumption, and disposal requirements under European REACH regulations (EC 1907/2006).

Overview

These AlphaLISA Toolbox Acceptor beads enable antibody binding studies or the detection of mouse IgG2b antibodies from various sources in various matrices. The IgG2 subtypes are the second most prevalent isotype and is responsible for thymus (TH1) mediated immune response to carbohydrate antigens.

These beads can be used in conjunction with Alpha Donor beads for use in AlphaLISA no-wash assays for isotyping or antibody binding studies. In a typical AlphaLISA assay, 1 mg of Acceptor beads is sufficient to run 1,000-2,000 wells using a 50 µL reaction volume.

Features:

  • No-wash steps, no separation steps
  • Ease-of-use: few addition steps, fast assay development
  • Broad range of affinities: detect strong or weak interactions, from pM to mM affinity
  • Distance: measure very large protein or antibody complexes – spanning up to 200 nm or more
  • High avidity: multiple binding sites on each bead enables use of nanomolar concentrations of antibodies or proteins, as well as use of low affinity binders

 

AlphaScreen™ and AlphaLISA™ are bead-based assay technologies used to study biomolecular interactions in a microplate format. The acronym "Alpha" stands for amplified luminescent proximity homogeneous assay. As the name implies, some of the key features of these technologies are that they are non-radioactive, homogeneous proximity assays. Binding of molecules captured on the beads leads to an energy transfer from one bead to the other, ultimately producing a luminescent/fluorescent signal. To understand how a signal is produced, one must begin with an understanding of the beads. AlphaScreen and AlphaLISA assays require two bead types: Donor beads and Acceptor beads. Each bead type contains a different proprietary mixture of chemicals, which are key elements of the AlphaScreen technology. Donor beads contain a photosensitizer, phthalocyanine, which converts ambient oxygen to an excited and reactive form of O2, singlet oxygen, upon illumination at 680 nm. Please note that singlet oxygen is not a radical; it is molecular oxygen with a single excited electron. Like other excited molecules, singlet oxygen has a limited lifetime prior to falling back to ground state. Within its 4 µsec half-life, singlet oxygen can diffuse approximately 200 nm in solution. If an Acceptor bead is within that proximity, energy is transferred from the singlet oxygen to thioxene derivatives within the Acceptor bead, subsequently culminating in light production at 520-620 nm (AlphaScreen) or at 615 nm (AlphaLISA). In the absence of an Acceptor bead, singlet oxygen falls to ground state and no signal is produced. This proximity-dependent chemical energy transfer is the basis for AlphaScreen's homogeneous nature.

Specifications

Application
Protein-Protein Interaction
Automation Compatible
Yes
Brand
AlphaLISA
Detection Modality
Alpha
Host Species
Mouse
Product Group
Beads
Shipping Conditions
Shipped in Blue Ice
Target
IgG2b
Target Class
Biologics
Target Species
Mouse
Technology
Alpha
Unit Size
250 µg

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