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A propos de cet article
Conjugate:
unconjugated
Clone:
polyclonal
Application:
ELISA (i)
Citations:
71
Service technique
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Laissez-nous vous aiderbiological source
rabbit
Quality Level
conjugate
unconjugated
antibody form
whole antiserum
antibody product type
primary antibodies
clone
polyclonal
contains
15 mM sodium azide
technique(s)
indirect ELISA: 1:8,000
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Immunogen
A DNP-BSA conjugate
Application
Anti-DNP antibody produced in rabbit was used to tag derivatized protein carbonyl groups in plasma by ELISA. It was used for differential cell count of zona-free blastocysts in IVF embryos.
Biochem/physiol Actions
2,4-Dinitrophenyl is an oxidative phosphorylation inhibitor and hinders adenosine triphosphate (ATP) synthesis. Due to its low excretion rate, 2,4-dinitrophenyl is considered toxic to human. It increases electron transportation, respiration and overall metabolism.
Analysis Note
Antiserum is tested for specificity and titer by immunoelectrophoresis; treated to remove lipoproteins..
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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Classe de stockage
10 - Combustible liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
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Contenu apparenté
Instructions
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Antimicrobial agents and chemotherapy, 48(1), 110-115 (2003-12-25)
Salivary histatins (Hsts) are potent candidacidal proteins that induce a nonlytic form of cell death in Candida albicans accompanied by loss of mean cell volume, cell cycle arrest, and elevation of intracellular levels of reactive oxygen species (ROS). Since these
Jens Nagel et al.
Chromosoma, 121(4), 353-367 (2012-03-15)
The large-scale chromatin organization of retrovirus and retroviral gene vector integration loci has attracted little attention so far. We compared the nuclear organization of transcribed integration loci with the corresponding loci on the homologous chromosomes. Loci containing gamma-retroviral gene transfer