IgG2a ELISA Kit
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- Target See all IgG2a products
- IgG2a
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Reactivity
- Rat
- Detection Method
- Colorimetric
- Method Type
- Sandwich ELISA
- Detection Range
- 0.78-50 ng/mL
- Minimum Detection Limit
- 0.78 ng/mL
- Application
- ELISA
- Purpose
- This assay employs the quantitative sandwich enzyme immunoassay technique for the quantitative detection of rat IgG2a.
- Sample Type
- Cell Culture Supernatant, Plasma, Serum
- Analytical Method
- Quantitative
- Specificity
- IgG2a
- Components
- plate, standard, diluent
- Material not included
- pipettes, tubes, reader
- Featured
- Discover our best selling IgG2a ELISA Kit
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IgG2a ELISA Kit
Reactivity: Mouse Colorimetric Sandwich ELISA 12.5 ng/mL - 400 ng/mL Plasma, Serum, Urine
IgG2a ELISA KitReactivity: Guinea Pig Colorimetric Sandwich ELISA 0.781 ng/mL - 50 ng/mL Plasma, Serum, Tissue Homogenate
IgG2a ELISA KitReactivity: Mouse Colorimetric Sandwich ELISA 0.15 ng/mL - 10 ng/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
IgG2a ELISA KitReactivity: Rat Colorimetric Competition ELISA 246.91 ng/mL - 20000 ng/mL Plasma, Serum
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- Sample Volume
- 100 μL
- Assay Time
- 3 - 4 h
- Plate
- Pre-coated
- Restrictions
- For Research Use only
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- Buffer
- 0.02 % sodium azide
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C
-
- Target See all IgG2a products
- IgG2a
- Abstract
- IgG2a Products
- Synonyms
- gamma-2a immunoglobulin heavy chain ELISA Kit, IgG-2a ELISA Kit
- Target Type
- Antibody
- Background
- Antibody isotyping is a critical and beneficial aspect of hybridoma development. This kit can identify six immunoglobulin heavy chain isotypes and two light chain isotypes in mice: IgA, IgM, IgG1, IgG2a, IgG2b, IgG3, kappa chain and lambda chain. It can accurately and specifically identify which heavy and light chain of the hybridoma samples is producing and if it is monoclonal or not. This kit is a powerful tool to isolate and characterize each potential clone.
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