产品详情
组分(Materials Provided)
IDComponentsSizeRAS103-C01Pre-coated Glycoprotein E (VZV) Microplate1 plateRAS103-C02Positive Control100 μLRAS103-C03Negative Control100 μLRAS103-C04HRP-Goat anti-Mouse IgG50 μLRAS103-C0510 x Washing Buffer50 mLRAS103-C06Dilution Buffer50 mLRAS103-C07Substrate Solution12 mLRAS103-C08Stop Solution7 mL产品概述(Product Overview)
Varicella-zoster virus (VZV) is a neurotropic virus belonging to the Herpesviridae family. Primary VZV infection causes chickenpox and is followed by a life-long latent infection established mainly in the cranial and dorsal root ganglia. Reactivation of the virus is often associated with shingles (herpes zoster).
Glycoprotein E (gE) is one of the known glycoproteins (gB, gC, gE, gH, gI, gK, gI) of VZV that is most abundantly expressed on the surface of virus and infected cells, playing an important role in viral replication and cell-to-cell spread. The strongly immunogenic gE can provide strong IgG signal in body fluid, which makes it ideal to be developed as an antigen for analysis of IgG antibodies. gE also demonstrates high potency as a vaccine immunogen and is formulated as the single viral envelope protein that constitutes the GSK VZV recombinant subunit vaccine Shingrix®.
应用说明(Application)
This kit is developed for titer detection of Anti-Varicella Zoster Virus Antibody IgG (gE) in mouse serum.
It is for research use only.
存储(Storage)
2-8℃
原理(Assay Principles)
This assay kit employs a standard indirect-ELISA format, providing a rapid detection of Anti-VZV gE antibodies in Mouse serum by Glycoprotein E (VZV). The Kit consists of Pre-coated Glycoprotein E (VZV) Microplate, an Positive Control, an Negative Control, an HRP-Anti-Goat anti mouse IgG secondary antibody.
Your experiment will include 4 simple steps:
a) The samples and Control are diluted by Dilution Buffer. Add your sample to the plate.
b) Add diluted Secondary antibody HRP-Goat anti-Mouse IgG to the plate. The Secondary antibody is diluted by Dilution Buffer.
c) Wash the plate and add TMB or other colorimetric HRP substrate.
d) Stop the substrate reaction by add diluted acid. Absorbance (OD) is calculate as the absorbance at 450 nm minus the absorbance at 630 nm to remove background prior to statistical analysis. The OD Value reflects the amount of antibody bound.
质量管理控制体系(QMS)
产品展示
典型数据-Typical Data
Please refer to DS document for the assay protocol.
For determination of antibody titer: the positive sample was diluted with a gradient, and the antibody titer of the sample corresponds to the highest dilution factor that still yields a positive reading.
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