CMV Mosaic

Cytomegalo Virus Mosaic Recombinant

The E.Coli derived Recombinant Cytomegalo Virus Mosaic contains the multiple epitopes from P150-P52-P38-P65-P28 having a molecular weight of 40kDa.
The CMV Mosaic is fused to a 6xHis tag and purified by proprietary chromatographic technique.

Shipped with Ice Packs
Cat. No.
BT1263
Source
Escherichia Coli.
Appearance
Sterile filtered colorless solution.

CMV gB

Cytomegalo Virus gB Recombinant

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, the protein weight is 6.5kDa, having a total weight of 32.5 kDa.
Shipped with Ice Packs
Cat. No.
BT1363
Source
Escherichia Coli.
Appearance

CMV Pp150

Cytomegalo Virus Pp150 (UL32) Recombinant

The E.Coli derived recombinant protein contains the CMV Pp150 (UL32) immunodominant regions, 1011-1048 amino acids.
Shipped with Ice Packs
Cat. No.
BT1447
Source
Escherichia Coli.
Appearance

CMV Pp28

Cytomegalo Virus Pp28 (UL99) Recombinant

The E.Coli derived recombinant protein contains the CMV Pp28 (UL99) immunodominant regions, 130-160 amino acids.
Shipped with Ice Packs
Cat. No.
BT1544
Source
Escherichia Coli.
Appearance

CMV Pp38

Cytomegalo Virus Pp38 (UL80a) Recombinant

The E.Coli derived 52.8kDa recombinant protein contains the CMV Pp38 (UL80a) immunodominant regions, 117-373 amino acids and fused to a GST-Tag at C-terminus.
Shipped with Ice Packs
Cat. No.
BT1611
Source
Escherichia Coli.
Appearance

CMV Pp52

Cytomegalo Virus Pp52 (UL44) Recombinant

The E.coli derived 51 kDa recombinant protein contains the CMV Pp52 (UL44) immunodominant regions, 202-434 amino acids. Recombinant CMV-Pp52 is fused to a 26 kDa GST tag.
Shipped with Ice Packs
Cat. No.
BT1692
Source
Escherichia Coli.
Appearance

CMV Pp65

Cytomegalo Virus Pp65 (UL83) Recombinant

The E.Coli derived 52.2 kDa recombinant protein contains the CMV Pp65 (UL83) immunodominant regions, 297-510 amino acids. Recombinant CMV-Pp65 is fused to a 26 kDa GST tag.

Shipped with Ice Packs
Cat. No.
BT1758
Source
Escherichia Coli.
Appearance

CMV Pp65, 561 a.a.

Cytomegalo Virus Pp65(UL83), 561 a.a.Recombinant

The E.Coli derived 62.8 kDa recombinant protein contains the CMV Pp65 (UL83) immunodominant regions, having 561 amino acids.

Shipped with Ice Packs
Cat. No.
BT1873
Source
Escherichia Coli.
Appearance
Definition and Classification

Cytomegalovirus (CMV) is a genus of viruses in the order Herpesvirales, within the family Herpesviridae, and the subfamily Betaherpesvirinae . The term “cytomegalo” is derived from Greek, meaning “cell” (cyto-) and “large” (megalo-), reflecting the virus’s ability to cause enlarged cells . CMV includes several species, with Human cytomegalovirus (HCMV) or Human betaherpesvirus 5 (HHV-5) being the most studied .

Biological Properties

CMV is a double-stranded DNA virus with an icosahedral shape, measuring 150 to 200 nm in diameter . It has four fundamental structural elements: an outer lipid envelope, tegument, nucleocapsid, and an internal nucleoprotein core containing its genome . The virus is ubiquitous, with a seroprevalence rate varying widely based on geographic location, age, and socioeconomic status . CMV can infect various human cells, including fibroblasts, epithelial cells, endothelial cells, smooth muscle cells, and monocytes .

Biological Functions

CMV plays a significant role in immune responses and pathogen recognition. It can generate a robust immune response and establish a latent infection in immunocompromised individuals . The virus can evade the immune system by manipulating host cell signaling and immune responses, allowing it to persist in the host . CMV-specific CD8+ cytotoxic T lymphocytes and CD4+ T cells are crucial for controlling primary infection and reactivation from latency .

Modes of Action

CMV interacts with various molecules and cells through complex mechanisms. It can bind to host cell receptors, leading to viral entry and subsequent replication . The virus manipulates host cell signaling pathways to establish and maintain latency, as well as to reactivate when conditions are favorable . CMV’s tegument proteins, such as pp65, play a crucial role in modulating host immune responses and facilitating viral replication .

Regulatory Mechanisms

The expression and activity of CMV are tightly regulated through various mechanisms. Transcriptional regulation involves the interaction of viral proteins with host transcription factors to control viral gene expression . Post-translational modifications, such as phosphorylation and ubiquitination, also play a role in modulating the activity of viral proteins and ensuring efficient viral replication . Additionally, CMV can alter host cell signaling cascades to create a favorable environment for its replication .

Applications in Biomedical Research

CMV has significant applications in biomedical research, diagnostic tools, and therapeutic strategies. It serves as a model for studying viral latency, immune evasion, and host-pathogen interactions . CMV is also used in the development of antiviral drugs and vaccines . Novel approaches, such as gene editing and RNA interference, are being explored to target CMV and prevent its reactivation in immunocompromised individuals . Diagnostic tools, including serology and molecular assays, are essential for detecting CMV infections .

Role in the Life Cycle

CMV plays a crucial role throughout the life cycle, from development to aging and disease. It is acquired early in life, often during childhood, through exposure to infected bodily fluids . The virus establishes a latent infection in various host cells, with periodic reactivations controlled by the immune system . In immunocompromised individuals, CMV reactivation can lead to severe disease, including pneumonia, hepatitis, and retinitis . CMV is also a leading cause of congenital infections, resulting in hearing loss, developmental delays, and other complications in newborns .

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