Zika Ectodomain

Zika Ectodomain Recombinant

Recombinant Zika Ectodomain is a glycosylated protein, produced using baculovirus vectors in insect cells and its Mw is approximately 45kDa.
The Zika Ectodomain is a recombinant protein of the ectodomain of the envelope protein from the Suriname Zika virus strain.
Shipped with Ice Packs
Cat. No.
BT10790
Source
Baculovirus Insect Cells.
Appearance
Sterile Filtered solution.

Zika Envelope

Zika Envelope Recombinant

The E.Coli derived Recombinant Zika Envelope protein having a Mw of 19kDa .The Zika Envelope protein is fused to a 6xHis tag at C-terminus and purified by proprietary chromatographic technique.

Shipped with Ice Packs
Cat. No.
BT10824
Source
Escherichia Coli.
Appearance
Sterile Filtered solution.

Zika Envelope Domain-3

Zika Envelope Domain-III Recombinant

The E.Coli derived Zika Envelope domain-III is a non-glycosylated polypeptide chain having a molecular mass of 11 kDa and fused to a His tag at N-terminus.
Shipped with Ice Packs
Cat. No.
BT10939
Source
Escherichia Coli.
Appearance
Sterile Filtered White lyophilized (freeze-dried) powder.

Zika Envelope F.Length

Zika Envelope Full Length Protein Recombinant

The E.Coli derived Recombinant Zika Envelope protein 40-400 a.a. having an Mw of 45kDa. The Zika Envelope full length protein without a C-terminal hydrophobic region.

The Zika Envelope full length protein is fused to a 6xHis tag at C-terminus and purified by proprietary chromatographic technique.

Shipped with Ice Packs
Cat. No.
BT11033
Source
Escherichia Coli.
Appearance
Sterile Filtered solution.

Zika Envelope N

Zika Envelope N-Terminal Recombinant

Zika Envelope N protein is a peptide partially derived from zika envelope N terminal containing 270 amino acids, having an Mw of 30kDa and the Isoelectric point is 6.37.
The Zika Envelope N protein is fused to a 6xHis tag at C-terminus and purified by proprietary chromatographic technique.

Shipped with Ice Packs
Cat. No.
BT11130
Source
Escherichia Coli.
Appearance
Sterile Filtered solution.

Zika Envelope, sf9

Zika Envelope Recombinant, sf9

Sf9 derived recombinant Zika Envelope protein, having an Mw of approximately 50kDa.
The Zika Envelope protein is fused to a 6xHis tag and purified by proprietary chromatographic technique.
Shipped with Ice Packs
Cat. No.
BT11221
Source
Sf9, Baculovirus cells.
Appearance
Sterile Filtered solution.

Zika NS1

Zika NS1 Protein Recombinant

The E.Coli derived Recombinant Zika NS1 protein (Strain: ZikaSPH2015) having an Mw of 45kDa is derived from the full length Zika NS1 protein.
The Zika NS1 protein is fused to a 6xHis tag at C-terminus and purified by proprietary chromatographic technique.
Shipped with Ice Packs
Cat. No.
BT11286
Source
Escherichia Coli.
Appearance
Sterile Filtered solution.

Zika NS1, HEK

Zika NS1 Protein Recombinant, HEK

The HEK derived recombinant Zika NS1 protein strain MR-766 (Prototype, Uganda, 1947, GenBank accession number AY632535).
The Zika NS1 protein is fused to a 6xHis tag at C-terminus and purified by proprietary chromatographic technique.
Shipped with Ice Packs
Cat. No.
BT11367
Source
Human Embryonic Kidney 293 cells.
Appearance
Sterile Filtered solution.

Zika NS1, sf9

Zika NS1 Protein Recombinant, sf9

Sf9 derived recombinant Zika NS1 protein.
The Zika NS1 protein is fused to a 6xHis tag and purified by proprietary chromatographic technique.
Shipped with Ice Packs
Cat. No.
BT12016
Source
Sf9, Baculovirus cells.
Appearance
Sterile Filtered solution.
Definition and Classification

The Zika virus (ZIKV) is a mosquito-borne flavivirus that belongs to the family Flaviviridae and the genus Flavivirus . It is closely related to other flaviviruses such as dengue, yellow fever, Japanese encephalitis, and West Nile viruses . ZIKV was first identified in a rhesus monkey in Uganda’s Zika Forest in 1947 and later in humans in 1952 .

Biological Properties

Key Biological Properties: ZIKV is an enveloped, icosahedral virus with a nonsegmented, single-stranded, positive-sense RNA genome of approximately 10.8 kilobases . The genome encodes a polyprotein that is cleaved into three structural proteins (capsid, envelope, and membrane) and seven nonstructural proteins .

Expression Patterns and Tissue Distribution: ZIKV primarily infects and replicates in various tissues, including the placenta and brain . It has been found in neural progenitor cells, astrocytes, and microglial cells .

Biological Functions

Primary Biological Functions: ZIKV’s primary function is to replicate within host cells and produce viral progeny. It plays a significant role in immune responses and pathogen recognition by interacting with host cell receptors and immune cells .

Role in Immune Responses and Pathogen Recognition: ZIKV infection triggers immune responses, including the production of neutralizing antibodies and activation of immune cells. The virus can evade immune detection by modulating host immune pathways .

Modes of Action

Mechanisms with Other Molecules and Cells: ZIKV interacts with host cell receptors, such as the envelope glycoprotein, to attach and enter human cells . It exploits cellular machinery for replication and assembly of new virions .

Binding Partners and Downstream Signaling Cascades: The virus binds to specific receptors on host cells, leading to endocytosis and release of viral RNA into the cytoplasm. This triggers downstream signaling cascades that facilitate viral replication and immune evasion .

Regulatory Mechanisms

Regulatory Mechanisms Controlling Expression and Activity: ZIKV infection activates the antioxidant nuclear factor erythroid 2-related factor 2 (Nrf2), which precedes oxidative stress . The virus also modulates host cell metabolism and homeostasis to promote its replication .

Transcriptional Regulation and Post-Translational Modifications: ZIKV relies on host cell machinery for transcription and translation of its genome. Post-translational modifications of viral proteins are essential for viral assembly and maturation .

Applications

Biomedical Research: ZIKV has become a focal point in biomedical research due to its association with severe congenital anomalies and neurological disorders . Research efforts aim to understand its pathogenesis, develop diagnostic tools, and identify therapeutic targets .

Diagnostic Tools: Diagnostic methods for ZIKV include molecular techniques such as RT-PCR to detect viral RNA and serological tests to identify antibodies .

Therapeutic Strategies: Current therapeutic strategies focus on developing antiviral drugs and vaccines to prevent ZIKV infection. Several candidate vaccines are in various stages of clinical trials .

Role in the Life Cycle

Role Throughout the Life Cycle: ZIKV is maintained in an enzootic cycle involving forest-dwelling Aedes mosquitoes and non-human primates . In humans, the virus can be transmitted through mosquito bites, sexual contact, and from mother to fetus . The virus’s ability to infect and replicate in various tissues, including the placenta and brain, contributes to its pathogenicity and impact on human health .

ZIKV’s life cycle involves attachment to host cell receptors, entry via endocytosis, replication of viral RNA, assembly of new virions, and release from the host cell . The virus’s dependence on host cell machinery for replication and its ability to evade immune responses are critical for its survival and propagation .

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