M8642
Anti-Maus-IgG (Gesamtmolekül)
affinity isolated antibody, lyophilized powder
Synonym(e):
Anti-mouse antibody
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About This Item
Empfohlene Produkte
Biologische Quelle
goat
Qualitätsniveau
200
300
Konjugat
unconjugated
Antikörperform
affinity isolated antibody
Antikörper-Produkttyp
secondary antibodies
Klon
polyclonal
Form
lyophilized powder
Methode(n)
Ouchterlony double diffusion: suitable
Lagertemp.
2-8°C
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Allgemeine Beschreibung
IgG antibody subtype is the most abundant serum immunoglobulins of the immune system. It is secreted by B cells and is found in blood and extracellular fluids and provides protection from infections caused by bacteria, fungi and viruses. Maternal IgG is transferred to fetus through the placenta that is vital for immune defence of the neonate against infections
Anti-Mouse IgG (whole molecule) antibody recognizes IgG1, G2a, G2b, and G3, mouse IgM and IgA. The identity and purity of affinity isolated antibody is established by immunoelectrophoresis.
Anti-Mouse IgG (whole molecule) antibody recognizes IgG1, G2a, G2b, and G3, mouse IgM and IgA. The identity and purity of affinity isolated antibody is established by immunoelectrophoresis.
Immunogen
Pooled normal mouse serum
Anwendung
Anti-Mouse IgG (whole molecule) antibody was used as secondary antibody in immunoblotting at a working dilution of 1:1000. The antibody was used in ELISA and RIA in various studies.
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Enzyme-linked immunosorbent assay (1 paper)
Enzyme-linked immunosorbent assay (1 paper)
Physikalische Form
Lyophilized from 0.01 M sodium phosphate, 0.015 M sodium chloride, pH 7.2
Rekonstituierung
Reconstitute with 0.135 M sodium chloride.
Haftungsausschluss
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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Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
Analysenzertifikate (COA)
Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.
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Kristian M Forbes et al.
PloS one, 9(3), e91113-e91113 (2014-03-14)
Marked variation occurs in both seasonal and multiannual population density peaks of northern European small mammal species, including voles. The availability of dietary proteins is a key factor limiting the population growth of herbivore species. The objective of this study
Govert J van Dam et al.
Experimental parasitology, 135(2), 274-282 (2013-07-16)
An earlier reported laboratory assay, performed in The Netherlands, to diagnose Schistosoma infections by detection of the parasite antigen CAA in serum was converted to a more user-friendly format with dry reagents. The improved assay requires less equipment and allows
Orhan Kankavi
Acta biochimica Polonica, 50(4), 1057-1064 (2004-01-24)
The presence of surfactant proteins was investigated in the human organ of Corti, Eustachian tube and kidney tissues. It has previously been shown that lamellar bodies are present in hairy cells of organ of Corti, in the cytoplasm of secretory
Jusung Oh et al.
Theranostics, 8(12), 3189-3197 (2018-06-23)
The immunochromatographic (ICA) assay is a highly promising platform for rapid and simple detection of C-reactive protein (CRP) which is an indicator of the different phases of various diseases, as well as of inflammation and infection. However, the hook effect
D R Jayne et al.
Clinical and experimental immunology, 84(3), 476-481 (1991-06-01)
The IgG subclass distribution for both ANCA-specific, and total IgG subclasses, of sera from 48 patients with active systemic vasculitis was determined by solid-phase assay using monoclonal anti-human subclass reagents. To control for varying performance of the subclass reagents, the
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