Glutamate Decarboxylase 2 (GAD2) Antibody Pair

A comprehensive antibody pair for developing sandwich ELISA assays to detect Glutamate Decarboxylase 2 (GAD2).

Kit Components:

– Capture Antibody (200 µg or 400 µg)
– Biotin-Conjugated Detection Antibody (50 µg or 100 µg)
– Standard (2 µg or 10 µg)

Assay Information:

– Suitable for 5 or 10 x 96 tests

Recommended Accessories:

– Cat No : 100029 Antibody Pair Support Kit (Sandwich Method)

Cat. No: 100029

Sizes : 5 × 96 tests
10 × 96 tests

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Description

Target Glutamate Decarboxylase 2 (GAD2)
Reactivity Rat
Tested Applications ELISA
Recommended dilutions Dilute the Capture Antibody 125-fold with Coating Buffer.
Dilute the Biotin-Conjugated Detection Antibody 200-fold with Detection Antibody Diluent.Optimal dilutions/concentrations should be determined by the end user.
Form Liquid (Capture Antibody and Detection Antibody)
Reconstitution Reconstitute the standard with Standard Diluent. The volume, and therefore standard concentration, should be determined by the end user.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC Q05683 (UniProt, ExPASy)
UniProt Entry Name DCE2_RAT
Gene Symbol GAD2
GeneID 24380
KEGG rno:24380
Ensembl ENSRNOG00000018200
String 10116.ENSRNOP00000024901
Buffer The Capture and Detection Antibody both contain 0.1% sodium azide.
Standard Form Lyophilized
Assay Type Sandwich
Capture Antibody Conjugation Unconjugated
Detection Antibody Conjugation Biotin
Concentration Capture Antibody: 0.5 mg/ml
Biotin-Conjugated Detection Antibody: 0.2 mg/ml
Availability Please enquire.
Note This product is for research use only.
Directions for use Bring all components to room temperature (18-25°C) and briefly spin or centrifuge the vials before use. Working solutions should be prepared and used immediately.
Recommended Procedure:

  1. Dilute the Capture Antibody to working concentration using Coating Buffer. Immediately coat the 96-well plate with diluted Capture Antibody (100 µl per well). Seal the plate and incubate at 4 °C overnight or at 37 °C for 2 hours
  2. Aspirate the wells and wash with Wash Buffer (350 µl per well) and allow to soak for 1-2 min. Remove the liquid by inverting and tapping the plate on to absorbent paper.
  3. Block the plate with Blocking Buffer (200 µl per well) at 37 °C for 1.5 hours.
  4. Repeat the aspiration/wash process in Step 2.
  5. Add 100 µl of standards or sample into the appropriate wells. Cover with a plate sealer and incubate at 37 °C for 1 hour.
  6. Repeat the aspiration/wash process in Step 2.
  7. Add appropriately diluted Biotin-Conjugated Detection Antibody (100 µl per well). Cover the plate with a new plate sealer and incubate at 37 °C for 1 hour.
  8. Repeat the aspiration/wash process in Step 2.
  9. Add appropriately diluted Streptavidin HRP (100 µl per well). Cover the plate with a new plate sealer and incubate at 37 °C for 30 min.
  10. Repeat the aspiration/wash process in Step 2.
  11. Add Substrate Solution (90 µl per well). Cover the plate with a new plate sealer and incubate at 37 °C for 10-20 min. Keep the plate in the dark and avoid exposure to light.
  12. Add Stop Solution (50 µl per well). Tap the side of the plate to ensure thorough mixing.
  13. Measure the absorbance immediately using a microplate reader set at 450 nm.

Research Articles on Glutamate Decarboxylase 2 (GAD2)

Data sheet

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SDS

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