产品名称 Alpha-2-Plasmin Inhibitor (a2PI) Antibody Pair
产品货号 Catalogue No: abx370735
产品价格 现货询价,电话:010-67529703
产品规格 Available Options * Size: 5 × 96 tests 10 × 96 tests
产品品牌 abbexa
产品概述
产品详情
Alpha-2-Plasmin Inhibitor (a2PI) Antibody Pair for use in Sandwich ELISA assay development. This antibody pair contains:
  • Alpha-2-Plasmin Inhibitor (a2PI) capture antibody,
  • Alpha-2-Plasmin Inhibitor (a2PI) biotin-conjugated detection antibody,
  • Alpha-2-Plasmin Inhibitor (a2PI) standard.
It is recommended to use this antibody pair with abx098958 Antibody Pair Support Kit (Sandwich Method).
Target Alpha-2-Plasmin Inhibitor (a2PI)
Reactivity Mouse
Tested Applications ELISA
Recommended dilutions Dilute the Capture Antibody with Coating Buffer.
Dilute the biotin-conjugated Detection Antibody 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.
Standard Form Lyophilized
ELISA Type Sandwich
Capture Antibody Conjugation Unconjugated
Detection Antibody Conjugation Biotin
Buffer The capture and detection antibody both contain 0.1% sodium azide.
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.
Availability Shipped within 5-20 working days.
Note This product is for research use only.
产品资料 下载链接