discontinued

AR10547PU-N Hepatitis B E / HBeAg

Search for all "Hepatitis B E / HBeAg"

0.5 mg / €390.00

Quick Overview

Hepatitis B E / HBeAg

AR10547PU-N

Product Description for Hepatitis B E / HBeAg

Hepatitis B E / HBeAg.
Presentation: Purified

Properties for Hepatitis B E / HBeAg

Product Category Proteins & Growth Factors
Quantity 0.5 mg
Presentation Purified
Source E. coli
Shipping to Worldwide
PDF datasheet View Datasheet
Manufacturer Acris Antibodies GmbH
Material safety datasheet MSDS for Proteins (de)

Datasheet Extract

Purity >95% pure as determined by 10% PAGE (coomassie staining).
Purification Method: GS-4B Sepharose-Affinity Purification.
Application Antigen in ELISA and Western blots, excellent antigen for detection of HBV with minimal specificity problems.
Background Hepatitis B is one of a few known non-retroviralviruses which employ reverse transcriptionas a part of its replication process. (HIV, a completely unrelated virus, also uses reverse transcription, but it is a retrovirus.) HBV invades the cell by binding to surface receptor and become internalized. The viral core particles then migrate to the hepatocyte nucleus and the partially double-stranded, relaxed circular genomes (RC-DNA) are repaired to form a covalently closed circular DNA (cccDNA), which is the template for viral genomic and sub-genomic RNAs by cellular RNA polymerase II. Of these, the pregenomic RNA (pgRNA is selectively packaged into progeny capsids and is then reverse-transcribed into new RC-DNA. The core can either bud into the endoplasmic reticulum to be enveloped or exported from the cell or recycled back into the genome for conversion to cccDNA. 
Concentration 1 mg/ml
Storage Protein is shipped at ambient temperature.
Upon arrival, Store at -20°C. 
Please avoid freeze-thaw cycles. 
Shelf life: One year from despatch.
Description
Description:
E.coli derived recombinant. The protein contains the HBV HBe immunodominant region.
Specificity: Immunoreactive with sera of HBV-infected individuals.
Format
Purity:
>95% pure as determined by 10% PAGE (coomassie staining).
Purification Method: GS-4B Sepharose-Affinity Purification.
State:
25mM Tris-HCl pH 8.0, 1.5M Urea, 50% Glycerol.
Purified
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