Immunoglobulin G1 (IgG1) Antibody

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Catalogue No: abx227131
Price: US$319.00
(Size: 40 µl)
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IHC-P analysis showing IgG positive plasma cells in the case of IgG4-related chronic sclerosing sialoadenitis.
Immunoglobulin G1 (IgG1) Antibody Immunoglobulin G1 (IgG1) Antibody

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Datasheet SDS
Immunoglobulin G1 (IgG1) Antibody is a Rabbit Monoclonal antibody for the detection of IgG1.

Target Immunoglobulin G1 (IgG1)
Clonality Monoclonal
Clone V417
Reactivity Human
Tested Applications IHC
Host Rabbit
Recommended dilutions IHC-P: 1/100 - 1/300. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen Synthetic peptide derived from the internal domain of human IgG-1 chain C region.
Isotype IgG
Form Liquid
Purification Purified from rabbit antiserum by proprietary techniques.
Storage Store at 2-8°C.
UniProt Primary AC P01857 (UniProt, ExPASy) P01859 (UniProt, ExPASy) P01860 (UniProt, ExPASy) P01861 (UniProt, ExPASy)
Buffer 20 mM Tris-HCl, pH 8.0, containing 20 mg/ml BSA and 0.05% NaN3.
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Directions for use Suggested IHC-P Protocol
  1. Preparation of Tris-EDTA Buffer (10 mM Tris Base, 1 mM EDTA solution, 0.05% Tween-20, pH 9.0): Mix 1.21 g Tris and 0.37 g EDTA and dissolve in 700 ml of distilled water. Adjust pH to 9.0 with 1 M HCl and then add 0.5 ml of Tween-20 and mix thoroughly. Adjust the final volume to 1 L with distilled water. Store this solution at room temperature for up to 3 months or at 4 °C for long-term storage.
  2. Preparation of Wash Buffer: Use PBS, pH 7.0-7.5, containing 0.05% Tween-20.
  3. Deparaffinize the section in 3 changes of xylene, 10 minutes each.
  4. Wash the section in 96%, 80% and 70% ethanol, 10 minutes each.
  5. Rinse twice in distilled water, 5 minutes each.
  6. Block endogenous peroxidase by incubating the tissue in 3% hydrogen peroxide (H2O2) for 10 minutes.
  7. Wash twice in distilled water, 5 minutes each.
  8. Antigen retrieval: immerse the slide in Tris-EDTA buffer, pH 9.0, and incubate in a water bath for 25 minutes at 95-97 °C.
  9. Remove the slide from the water bath and allow to stand at room temperature (in Tris-EDTA buffer, pH 9.0) for 15 minutes.
  10. Rinse twice in distilled water, 5 minutes each.
  11. Wash twice in Wash Buffer, 5 minutes each.
  12. Incubate the section with primary antibody at 1/100 - 1/300 dilution for 1 hour in a closed wet chamber. It is recommended to use abx291502 Primary Antibody Diluent or a diluent containing protease-free BSA (> 1 mg/ml) to dilute this antibody.
  13. Wash 3 times with Wash Buffer, 5 minutes each.
  14. Add the secondary antibody and proceed to standard immunohistochemistry protocol (HRP - Peroxide - DAB). It is recommended to use abx291501 Rabbit and Mouse HRP/DAB Detection Kit.
  15. Wash 3 times in Wash Buffer, 5 minutes each.
  16. Apply the DAB chromagen for 1-3 minutes.
  17. Wash twice in water, 5 minutes each.
  18. Stain in hematoxylin for 5 minutes.
  19. Wash 3 times in water, 2 minutes each.
  20. Mount the slide for observation.
Research Articles on Immunoglobulin G1 (IgG1)


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