F2266
Anti-Mouse IgG (whole molecule) F(ab′)2 fragment–FITC antibody produced in sheep
affinity isolated antibody, buffered aqueous solution
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About This Item
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biological source
sheep
Quality Level
conjugate
FITC conjugate
antibody form
affinity isolated antibody
antibody product type
secondary antibodies
clone
polyclonal
form
buffered aqueous solution
technique(s)
direct immunofluorescence: 1:128
storage temp.
2-8°C
target post-translational modification
unmodified
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General description
IgGs are glycoprotein antibodies that regulate immunological defense mechanisms such as phagocytosis and inflammatory responses . Mouse IgGs have four distinct isotypes, namely, IgG1, IgG2a, IgG2b, and IgG3. IgG1 regulates complement fixation in mice . Anti-Mouse IgG (whole molecule) F(ab′)2 fragment-FITC antibodies are specific for mouse IgG subclasses G1, G2a, G2b, and G3 and do not react with serum proteins in rat.
Immunogen
Mouse IgG
Application
Anti-Mouse IgG (whole molecule) F(ab′)2 fragment-FITC antibody is suitable for use in flow cytometry, immunohistochemistry, indirect immunofluorescence, and immunohistochemistry .
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunohistochemistry (1 paper)
Immunohistochemistry (1 paper)
Other Notes
Antibody adsorbed with rat serum proteins.
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin and 15 mM sodium azide.
Preparation Note
Adsorbed to reduce background staining with rat samples.
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
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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A Mechaly et al.
Applied and environmental microbiology, 74(3), 818-822 (2007-10-30)
A single-chain Fv (scFv) antibody was developed and applied for efficient and specific detection of Bacillus anthracis spores. The antibody was isolated from a phage display library prepared from spleens of mice immunized with a water-soluble extract of the outer
C M Newman et al.
Arteriosclerosis, thrombosis, and vascular biology, 15(11), 2010-2018 (1995-11-01)
Osteopontin (OP) is a secreted glycoprotein that contains the Arg-Gly-Asp (RGD) cell-binding sequence that binds calcium and is chemotactic and adhesive for rat vascular smooth muscle cells (VSMCs). OP gene expression is upregulated in cultured rat VSMCs in vitro and
Y Yan et al.
Journal of immunology (Baltimore, Md. : 1950), 166(8), 5258-5264 (2001-04-06)
Donor leukocytes play a dual role in rejection and acceptance of transplanted organs. They provide the major stimulus for rejection, and their removal from the transplanted organ prolongs its survival. Paradoxically, administration of donor leukocytes also prolongs allograft survival provided
Hisashi Ueta et al.
Hepatology (Baltimore, Md.), 47(4), 1352-1362 (2008-01-29)
Donor dendritic cell (DC) migration and allosensitization in host secondary lymphoid organs after liver transplantation are ill defined. We used rat models to investigate graft-derived cells and intrahost allosensitization. Liver transplantation induced diffuse blood-borne migration of donor major histocompatibility class
Lech Kiedrowski et al.
Journal of neurochemistry, 90(1), 117-128 (2004-06-17)
Inhibition of Na(+),K(+)-ATPase during NMDA applications greatly increased NMDA-induced excitotoxicity in primary cultures of forebrain neurons (FNs), but not in cerebellar granule cells (CGCs). Because Na(+),K(+)-ATPase inhibition promotes reversal of plasmalemmal Na(+)/Ca(2+) exchangers, we compared the activities of reversed K(+)-independent
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