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CMV-gB (residues 11-67)

Cytomegalo Virus Glycoprotein B

recombinant, E. coli

Cat. No. Amount Price (EUR) Buy / Note
PR-1247 100 μg 207,00 Add to Basket/Quote Add to Notepad

For in vitro use only!

Shipping: shipped on blue ice

Storage Conditions: store at -20 °C
avoid freeze/thaw cycles

Shelf Life: 12 months

Molecular Weight: 32.5 kDa

Purity: > 95 % (SDS-PAGE)

Form: liquid (Supplied in 25 mM Tris-HCl pH 7.2, 1 mM EDTA and 50% glycerol)

Antigen in ELISA and Western blots, excellent antigen for detection of CMV with minimal specificity problems.

The E.coli derived recombinant artificial mosaic protein contains the CMV gB immunodominant regions 11-67 amino acids fused with a 26 kDa GST-tag.

Background: Human cytomegalovirus (HCMV), a member of the herpesvirus family, demonstrates cell specificity for virus assembly and release. The mechanisms for virus assembly and egress are still unclear, although attachment of membrane-bound viral glycoproteins to tegumented capsid is believed to play an important role in this process. The most abundant glycoprotein detected in the HCMV virion envelope is gB. HCMV gB is synthesized as a 105-kDa polypeptide and processed into a highly glycosylated 130-kDa precursor glycoprotein. After glycosylation, the gB precursor is cleaved by furin to produce a heterodimer protein (gp55 and gp116). gB is a type I glycoprotein containing a signal sequence, an extracellular or luminal domain, a transmembrane (TM) domain, and a 135-amino-acid cytoplasmic tail. The cytoplasmic tail contains a consensus casein kinase II (CKII) site, which is phosphorylated both in vitro and in vivo. Human CMV is currently classified into four genotypes on the basis of the nucleotide sequence of the gB region.

Specificity: Immunoreactive with sera of CMV-infected individuals.

Selected References:
Carraro et al. (2003) Single human cytomegalovirus gB genotype shed in multiple sites at the time of diagnosis in renal transplant recipients. J. Med. Virol. 70:240.
Lipes et al. (2002) The genotype of mice influences the autoimmune response to spliceosome proteins induced by cytomegalovirus gB immunization. Clin. Exp. Immunol. 129:19.
Lukacsi et al. (2001) Human cytomegalovirus gB genotype 1 is dominant in congenital infections in South Hungary. J. Med. Virol. 65:537.
Fish et al. (1998) Steady-state plasma membrane expression of human cytomegalovirus gB is determined by the phosphorylation state of Ser900. J. Virol. 72:6657.
Zipeto et al. (1998) Geographic and demographic differences in the frequency of human cytomegalovirus gB genotypes 1-4 in immunocompromised patients. AIDS. Res. Hum. Retroviruses. 14:533.
Rasmussen et al. (1997) Cytomegalovirus gB genotype distribution differs in human immunodeficiency virus-infected patients and immunocompromised allograft recipients. J. Infect. Dis. 175:179.