Anti-HCV subtype 1b NS5B protein antibody (1-14 aa) [8B2] (STJA0002824)

SPECIFICATIONS
ClonalityMonoclonal
HostMouse
ConjugationUnconjugated
IsotypeIgG1
ImmunogenRecombinant Hepatitis C Virus subtype 1b nonstructural protein 5B (NS5B) RNA-dependent RNA polymerase (RdRp). Mapped to amino acids 1-14 (SMSYTWTGALITPC)
STJA0002824
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General Information

Short DescriptionMouse monoclonal anti-HCV subtype 1b NS5B protein (1-14 aa) for use in ELISA and IP in Human and HCV samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsELISA/IP
HostMouse
ReactivityHuman/HCV
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone ID8B2
IsotypeIgG1
ConjugationUnconjugated
PurificationNA Protein GΒ purification NA
Dilution RangeVery weak antigen recognition in WBOptimal conditions for IP should be determined for each particular application Blocks the RNA-dependent RNA polymerase activity in vitro. Monoclonal antibody working titer has to be established practically for each
FormulationPBS pH 7.4, with 0.1% sodium azide
Storage InstructionStore at-20 to-70 Β°C upon receipt. Divide antibody into aliquots prior usage. Avoid multiple freeze-thaw cycles as product degradation may result.

Target Information

ImmunogenRecombinant Hepatitis C Virus subtype 1b nonstructural protein 5B (NS5B) RNA-dependent RNA polymerase (RdRp). Mapped to amino acids 1-14 (SMSYTWTGALITPC)
Immunogen Region1-14 aa
SpecificityHuman, HCV subtype 1b NS5B, Epitope mapped to amino acids 1-14 (SMSYTWTGALITPC)

Additional Info

Background Non-structural protein 5B (NS5B) represents the RNA-dependent RNA polymerase (RdRp) of Hepatitis C Virus, which is a small positive strand RNA virus in the family Flaviviridae. HCV is a major causative agent of acute and chronic hepatitis, hepatocellular carcinoma and liver cirrhosis. The single subunit RNA-dependent RNA polymerase is absolutely essential for the viral replication.

Information sourced from Uniprot.org

Citations

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