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Mouse anti Human IgG (class specific)

CAT: 0579-MAHu/IgGc/MAbSize: 0.2 mgDry Ice: NoHazardous: No
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CAT#:0579-MAHu/IgGc/MAbSize:0.2 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
The reactivity of the antiserum is restricted to isotype specific determinants on the Fc part of the IgG molecule. It reacts with the 4 subclasses of Human IgG, as tested in indirect binding enzyme immunoassay, immunoblotting, immunoprecipitation and indirect immunoperoxidase staining of cytoplasmic Ig. To identify the presence of IgG in Human serum, other body fluids, cell and tissue substrates and to determine its concentration in techniques as ELISA, indirect immunoperoxidase and indirect immunofluorescence staining of cytoplasmic IgG, and immunoblotting. The optimum working dilution is an assay-related characteristic and should always be determined by titration. For histochemical use optimum dilutions are mostly from 1:50 to 1:200; in ELISA from 1:500 upwards; in Western blotting from 1:1,000 upwards. These data should be interpreted as general recommendations only.
CAS Number
9007-83-4
Host
Mouse
Isotype
IgG1
Clone
NI 335 and NI 343
Source
Highly purified monoclonal IgG isolated from Human serum
Assay Principle
Indirect immunofluorescence,ELISA.
Form
Purified mouse IgG1 kappa lyophilized from a solution in phosphate buffered saline (pH 7,2); Nopreservative added, as it may interfere with the antibody activity; Noforeign protein added IgG concentration is 0,4 mg/mL No foreign proteins added
Precautions
This product is intended FOR RESEARCH USE ONLY, and FOR TESTS IN VITRO, not for use in diagnostic or therapeutic procedures involving Humans or animals. This datasheet is as accurate as reasonably achievable, but Nordic-MUbio accepts no liability for any inaccuracies or omissions in this information.
Storage Conditions
To identify the presence of IgG in Human serum, other body fluids, cell and tissue substrates and to determine its concentration in techniques as ELISA, indirect immunoperoxidase and indirect immunofluorescence staining of cytoplasmic IgG, and immunoblotting. The optimum working dilution is an assay-related characteristic and should always be determined by titration; For histochemical use optimum dilutions are mostly from 1:50 to 1:200; in ELISA from 1:500 upwards; in Western blotting from 1:1,000 upwards. These data should be interpreted as general recommendations only.

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