MAB10234
Anti-Hepatitis B Virus Surface Antigen Antibody, clone H21F8-1
ascites fluid, clone H21F8-1, Chemicon®
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Recommended Products
biological source
mouse
Quality Level
antibody form
ascites fluid
antibody product type
primary antibodies
clone
H21F8-1, monoclonal
species reactivity
human
manufacturer/tradename
Chemicon®
technique(s)
immunofluorescence: suitable
isotype
IgM
shipped in
wet ice
General description
Hepatitis B virus surface antigen is one of the earliest markers of infection with hepatitis B virus. Hepatitis B virus surface antigen is tested for in the differential diagnosis of hepatitis. It is the first detectable viral antigen to appear during infection with this virus; however, early in an infection, this antigen may not be present and it may be undetectable later in the infection as it is being cleared by the host.
Application
Anti-Hepatitis B Virus Surface Antigen Antibody, clone H21F8-1 detects level of Hepatitis B Virus Surface Antigen & has been published & validated for use in IF.
Storage and Stability
Stable for 12 months when stored at -20°C from date of shipment
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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Storage Class
10 - Combustible liquids
wgk_germany
WGK 1
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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Clinical Characteristics and Surgical Outcome in Hepatocellular Carcinoma without Hepatitis B Virus Surface Antigen or Hepatitis C Virus Antibody
Tanaka, Kuniya, et al
Annals of Surgical Oncology, [Epub ahead of print]-[Epub ahead of print] (2006)
Sang Hyun Nam et al.
Archives of pharmacal research, 29(11), 1042-1048 (2006-12-07)
Plasmid DNA vaccines encoding the hepatitis B virus (HBV) surface and hepatitis C virus (HCV) envelope antigens, respectively, were constructed, and attempt were made to find the possibility of a divalent vaccine against HBV and HCV. The expression of each
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