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Merck

G7777

Anti-Mouse IgG (whole molecule)–Gold antibody produced in goat

affinity isolated antibody, aqueous glycerol suspension, 10 nm (colloidal gold)

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.46
MDL number:
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Product Name

Anti-Mouse IgG (whole molecule)–Gold antibody produced in goat, affinity isolated antibody, aqueous glycerol suspension, 10 nm (colloidal gold)

biological source

goat

conjugate

gold conjugate

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

aqueous glycerol suspension

particle size

10 nm (colloidal gold)

storage temp.

2-8°C

target post-translational modification

unmodified

Quality Level

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Application

Anti-Mouse IgG (whole molecule)-Gold antibody is suitable for use in immunoelectron microscopy .

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.

General description

Immunoglobulin G (IgG) is a glycoprotein antibody that regulates immune responses such as phagocytosis and is also involved in the development of autoimmune diseases . Mouse IgGs have four distinct isotypes, namely, IgG1, IgG2a, IgG2b, and IgG3. IgG1 regulates complement fixation in mice . Anti-Mouse IgG (whole molecule)-Gold antibody is specific for mouse IgG.

Immunogen

Purified mouse IgG

Other Notes

Antibody adsorbed with human serum proteins.

Physical form

Conjugate is suspended in Tris buffered saline, pH 8.2, containing 1% (w/v) BSA, 30% (v/v) glycerol and 15 mM sodium azide.

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Storage Class

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Maria Gregori et al.
Nanomedicine : nanotechnology, biology, and medicine, 13(2), 723-732 (2016-11-05)
Aggregation of amyloid-β peptide (Aβ) is a key event in the pathogenesis of Alzheimer's disease (AD). We investigated the effects of nanoliposomes decorated with the retro-inverso peptide RI-OR2-TAT (Ac-rGffvlkGrrrrqrrkkrGy-NH2) on the aggregation and toxicity of Aβ. Remarkably low concentrations of
Yoshihisa Hirakawa et al.
Journal of cell science, 125(Pt 24), 6176-6184 (2012-10-06)
In plants, many nucleus-encoded proteins are targeted to both mitochondria and plastids, and this process is generally mediated by ambiguous N-terminal targeting sequences that are recognized by receptors on both organelles. In many algae, however, plastids were acquired by secondarily
Ke Chen et al.
Molecular biology and evolution, 31(8), 2194-2211 (2014-06-04)
Understanding genomic variation and detecting selection signatures in a genome under selection have been great challenges for a century. Activation, development/exhaustion of primordial follicles in mammalian ovary determines reproductive success, menopause/end of female reproductive life. However, molecular mechanisms underlying oogenesis
Xiaoman Zhang et al.
PloS one, 17(6), e0270634-e0270634 (2022-06-25)
Extracellular vesicles (EVs) have attracted much attention as potential diagnostic biomarkers for human diseases. Although both plasma and serum are utilized as a source of blood EVs, it remains unclear whether, how and to what extent the choice of plasma
S B Shah et al.
Chromosoma, 105(2), 111-121 (1996-08-01)
Immunoelectron microscopy with anti-nucleolin defined substructures within the multiple nucleoli of biosynthetically active stage II-III oocytes and within the nucleoli of relatively quiescent stage VI oocytes of Xenopus laevis. Dense fibrillar components (DFCs) of nucleoli from stage II-III oocytes consisted

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