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Key Documents

MAB10234

Sigma-Aldrich

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

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 Code

10 - Combustible liquids

WGK

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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