missing translation for 'onlineSavingsMsg'
Learn More
  1. Home
  2. Products
  3. Antibodies
  4. Antibody Panels and Kits
  5. DS98200

Invitrogen™ ELISA Assay Buffer (5X)

Catalog No. DS98200
Encompass
Change view
Click to view available options
Quantity:
200 mL
1 product options available for selection
Product selection table with 1 available options. Use arrow keys to navigate and Enter or Space to select.
Catalog No. Quantity
DS98200 200 mL
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 1 options available.
1 options
Catalog No. DS98200 Supplier Invitrogen™ Supplier No. DS98200
Only null left

Description

For use with antibody pairs (ELISA)

Concentrated 5X Assay Buffer for Antibody Pairs is intended to be used as:

  • Blocking reagent for ELISA plates
  • Diluent for ELISA standards and samples
  • Diluent for the detection antibody
  • Diluent for the HRP conjugate

Build Your Own Immunoassay, Cell Analysis, Immunoassays

Order Info

Shipping Condition: Wet Ice

Specifications

Applications ELISA
Quantity 200 mL
Content And Storage Buffer. Store at 2-8°C.
Form Concentrated
Shipping Condition Wet Ice

Frequently Asked Questions (FAQs)

How do I develop a sandwich ELISA using Cytosets?

Each CytoSets contains capture (coating) antibody, biotinlyated detection antibody, standard and Streptavidin-HRP. Other reagents required are listed in the CytoSets information sheet included with the kit and can be purshased from us separately (Antibody Pair Buffer kit CNB0011, 5x Assay Buffer DS98200, etc.). The information sheet also provides a specific procedure and illustrates an example standard curve which can be obtained when the specific procedure is followed. A general procedure is summarized here:

1) Coat the microplate with diluted capture (coating) antibody overnight at 2-8 degrees C; Wash the plate
2) Incubate standards or samples with the coated microplate; Wash the plate
3) Incubate diluted biotinlyated detection antibody with the plate; Wash the plate
4) Incubate Streptavidin-HRP with the plate for 15-45 minutes; Wash the plate
5) Incubate the plate with TMB substrate for 10-60 minutes and stop the reaction with Stop solution
6) Read microplate at 450 nm.

Investigators are advised to determine optimal buffer formulations, concentrations and incubation times for individual applications.

For Research Use Only. Not for use in diagnostic procedures.