Human IgG4 Fc. ELISA Specificity: (Hamilton et al., 1987) human IgG subclass 1- 0.08% human IgG subclass 2 - 0.01% human IgG subclass 3 - 0.04% human IgG subclass 4-100% Isoelectric Focusing: mean pI 7.7
Immunogen
Epitope: Fc fragment
Application
Mouse anti-Human IgG4 Antibody, clone HP6023, Fc is an antibody against Human IgG4 for use in ELISA, RIA & WB.
Research Category Secondary & Control Antibodies
Research Sub Category Fragment Specific Secondary Antibodies
This antibody employed as both a capture antibody and a detection antibody for human IgG subclass 4 in enzyme linked immunosorbent assays, radio-immunoassay and EIA affinity immunoblots (Papadea et al., 1985; Hamilton, et al., 1987).
Final working dilutions must be determined by end user.
Maintain at 2 -8°C for up to one year in undiluted aliquots.
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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The Journal of experimental medicine, 179(2), 757-762 (1994-02-01)
During antigen-induced immune responses, human B cells switch isotype from immunoglobulin M (IgM)-IgD to IgG1-4, IgA1-2, or IgE. In the human, no cytokines have yet been demonstrated to act as switch factors for IgG1, IgG2, and IgG3. In this paper
Journal of immunology (Baltimore, Md. : 1950), 183(6), 4067-4076 (2009-08-19)
Multiple sclerosis (MS) typically manifests in early to mid adulthood, but there is increasing recognition of pediatric-onset MS, aided by improvements in imaging techniques. The immunological mechanisms of disease are largely unexplored in pediatric-onset MS, in part because studies have
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