MAB8152
Anti-West Nile Virus/Kunjin Antibody, NS1, clone 3.1112G
ascites fluid, clone 3.1112G, Chemicon®
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
biological source
mouse
antibody form
ascites fluid
antibody product type
primary antibodies
clone
3.1112G, monoclonal
species reactivity
human
manufacturer/tradename
Chemicon®
technique(s)
ELISA: suitable
immunofluorescence: suitable
immunohistochemistry: suitable
western blot: suitable
isotype
IgM
shipped in
wet ice
Specificity
Specific for the non-structural protein 1 of West Nile/Kunjin virus. Kunjin (KUN) is very closely related to some strains of West Nile virus, and has been classified as a subtype of West Nile.
Immunogen
Epitope: NS1
Application
Immunofluorescence: 1:2 to 1:50
EIA 1:20 to 1:200
Western Blot 1:20 to 1:200
Immunohistochemistry
Optimal working dilutions must be determined by the end user.
EIA 1:20 to 1:200
Western Blot 1:20 to 1:200
Immunohistochemistry
Optimal working dilutions must be determined by the end user.
Research Category
Infectious Diseases
Infectious Diseases
Research Sub Category
Infectious Diseases - Viral
Infectious Diseases - Viral
This Anti-West Nile Virus/Kunjin Antibody, NS1, clone 3.1112G is validated for use in ELISA, IF, IH, WB for the detection of West Nile Virus/Kunjin.
Physical form
Ascites fluid with 0.1% sodium azide as a preservative.
Unpurified
Storage and Stability
Maintain for 2 years at -20°C from date of shipment. Aliquot to avoid repeated freezing and thawing. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Analysis Note
Control
West Nile Virus positive patient sample
West Nile Virus positive patient sample
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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
10 - Combustible liquids
wgk_germany
nwg
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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M A Loroño-Pino et al.
Clinical and vaccine immunology : CVI, 16(5), 749-755 (2009-03-27)
An epitope-blocking enzyme-linked immunosorbent assay (b-ELISA) was evaluated for the diagnosis of West Nile virus (WNV) infections in humans. Sera from patients diagnosed with WNV infections from an outbreak in 2003 in Colorado and from patients diagnosed with dengue virus
Replication of West Nile virus in equine peripheral blood mononuclear cells.
David Garcia-Tapia, Christie M Loiacono, Steven B Kleiboeker
Veterinary Immunology and Immunopathology null
Jeremy P Ledermann et al.
Clinical and vaccine immunology : CVI, 18(4), 580-587 (2011-02-25)
Primary West Nile virus (WNV) infections can be diagnosed using a number of tests that detect infectious particles, nucleic acid, and specific IgM and/or IgG antibodies. However, serological identification of the infecting agent in secondary or subsequent flavivirus infections is
Multiple amino acid changes at the first glycosylation motif in NS1 protein of West Nile virus are necessary for complete attenuation for mouse neuroinvasiveness.
Melissa C Whiteman,Jason A Wicker,Richard M Kinney,Claire Y-H Huang,Tom Solomon,Alan D T Barrett
Vaccine null
Carlos Machain-Williams et al.
Journal of wildlife diseases, 49(3), 690-693 (2013-06-20)
Surveillance for evidence of West Nile virus (WNV) infection in Morelet's crocodiles (Crocodylus moreletii) was conducted in Campeche State, Mexico, in 2007. Sera from 62 crocodiles (32 free-ranging and 30 captive) were assayed for antibodies to WNV by epitope-blocking enzyme-linked
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