Products

Equid herpesvirus cDNA and Antigen

Cat#

Product Name

Swiss Prot#

Size

Price (US$)

Order

PN0373

Recombinant Protein-Equid herpesvirus 1 Envelope glycoprotein D (a.a.35 to 402)

Q04245

100 µg

1195

Order

PN0374

Recombinant Protein-Equid herpesvirus 1 Immediate early protein (a.a.50 to 278)

Q5CCQ3

100 µg

1195

Order

PN0375

Recombinant Protein-Equid herpesvirus 9 Major capsid protein (a.a.400 to 800)

B7FEI5

100 µg

1195

Order

PN0376

Recombinant Protein-Equid herpesvirus 9 Envelope glycoprotein M (a.a.50 to 450)

B7FEJ4

100 µg

1195

Order

RPN0373

cDNA-Equid herpesvirus 1 Envelope glycoprotein D (a.a.35 to 402)

Q04245

2 µg

1835

Order

RPN0374

cDNA-Equid herpesvirus 1 Immediate early protein (a.a.50 to 278)

Q5CCQ3

2 µg

1140

Order

RPN0375

cDNA-Equid herpesvirus 9 Major capsid protein (a.a.400 to 800)

B7FEI5

2 µg

2000

Order

RPN0376

cDNA-Equid herpesvirus 9 Envelope glycoprotein M (a.a.50 to 450)

B7FEJ4

2 µg

2000

Order

Equid herpesvirus cDNA and recombinant antigen

  • Codon-optimized cDNA is cloned into E. coli expression vector with 6x His-tag at N-terminus and ready-to-use for recombinant protein production.
  • Recombinant protein applications: Western Blot may be used for other applications determined by the user.
  • Protein Purity: >90%, as determined by SDS-PAGE under reducing conditions.
  • Protein Activity: N/A
  • Protein Tag:  Contains A 6x histidine tag at N-terminus.
  • Protein Formulation: Liquid
  • Source: Produced from E. coli

Equid herpesvirus, also known as equine herpesvirus (EHV), is a genus of herpesviruses that infect horses and other equids. There are nine known types of equid herpesviruses, designated EHV-1 through EHV-9.

EHV-1 is the most common and widely studied type, and it is a major cause of respiratory disease, neurological disease, and reproductive problems in horses. EHV-1 can also cause abortions in pregnant mares. Other types of equid herpesviruses, such as EHV-2 and EHV-5, are typically associated with respiratory infections and mild disease.

Equid herpesviruses are highly contagious and can be transmitted through direct contact with infected horses, contaminated equipment or surfaces, and respiratory secretions. The viruses can remain latent in infected horses and reactivate during times of stress or immunosuppression, leading to the shedding of the virus and the potential for further transmission. There are vaccines available for some types of equid herpesviruses, but they do not provide complete protection and proper management and biosecurity practices are also important in preventing the spread of the virus.

Equid herpesvirus (EHV) is a virus that affects horses and other equidae. There are several different strains of EHV, including EHV-1 and EHV-4, which can cause a range of symptoms, from mild respiratory illness to more severe conditions such as abortion and neurological disease. Some strains of EHV can also cause abortion in mares and respiratory disease in foals. EHV is highly contagious and can be spread through direct contact with an infected animal, as well as through contact with contaminated equipment, clothing, and feed. Vaccination is an effective way to prevent infection with EHV, and early detection and quarantine measures can help to control outbreaks.

The genome of Equid herpesvirus (EHV) is the complete set of genetic information that makes up the virus. The EHV genome is made up of double-stranded DNA and is organized into a linear chromosome. The EHV genome is relatively large and complex, with a size of around 150-200 kbp and contains more than 150 open reading frames (ORF) encoding various viral proteins.

EHV-1 and EHV-4 are the two main strains that cause disease in horses and other equidae. The genome sequences of these two strains have been fully characterized and are available in public databases such as GenBank.

An antigen is a substance that can stimulate an immune response in the body, such as the production of antibodies. Equid herpesvirus (EHV) antigen refers specifically to a protein or other component of the EHV virus that can trigger an immune response in horses and other equidae.

EHV antigen can be used as a diagnostic tool to detect the presence of the virus in a horse’s blood or other bodily fluids, using techniques such as ELISA (Enzyme-Linked ImmunoSorbent Assay) or PCR (polymerase chain reaction). EHV antigen can also be used as a component in a vaccine to help stimulate an immune response and protect against infection with the virus.EHV vaccines, either in the form of killed or modified-live virus, are the most common form of prophylaxis against EHV. The vaccines are designed to target specific strains of the virus, such as EHV-1 and EHV-4, which are known to cause the most severe forms of disease.

Equid herpesvirus (EHV) has several antigens associated with its structure and function. These include glycoprotein B, glycoprotein C, glycoprotein D, glycoprotein E, and glycoprotein I. Additionally, EHV also expresses several nonstructural proteins, such as the immediate-early protein (IE), early proteins (E), and late proteins (L). These antigens are the targets of the immune response in infected horses and are used in diagnostic tests for EHV infection.

Equid herpesvirus (EHV) has several structural and nonstructural proteins, including envelope glycoprotein D, immediate early protein, major capsid protein, and envelope glycoprotein M.

The envelope glycoprotein D (gD) is an important component of the virus envelope that is involved in viral entry and cell-to-cell spread. The immediate early protein (IE) is an important regulator of the virus life cycle, and it helps to activate the expression of early and late genes. The major capsid protein is a structural protein that forms the capsid of the virus particle and is involved in protecting the viral genome.

The envelope glycoprotein M (gM) is another component of the virus envelope and is involved in virus assembly and release. It is also important for the spread of the virus from cell to cell.

These proteins are important targets for the host immune response and are commonly used in diagnostic tests to detect EHV infection in horses.

The genome of Equid herpesvirus (EHV) is the complete set of genetic information that makes up the virus. The EHV genome is made up of double-stranded DNA and is organized into a linear chromosome. The EHV genome is relatively large and complex, with a size of around 150-200 kbp and contains more than 150 open reading frames (ORF) encoding various viral proteins.

EHV-1 and EHV-4 are the two main strains that cause disease in horses and other equidae. The genome sequences of these two strains have been fully characterized and are available in public databases such as GenBank.

The study of the EHV genome is important for understanding the genetic makeup of the virus, which can help in the development of diagnostic tests, vaccines, and antiviral treatments. Additionally, the genetic information in the genome of EHV can be used for phylogenetic analysis, which can provide insight into the evolution and spread of the virus.

Equid herpesvirus is a group of herpesviruses that infect horses and cause a range of clinical signs, including respiratory disease, abortion, and neurological disorders. The virus is composed of several proteins, each with unique functions in the virus’s lifecycle and pathogenesis.

One of the most important proteins of equid herpesvirus is the Envelope Glycoprotein D, which is involved in host cell recognition and viral entry. The Immediate Early Protein is a transcription factor that regulates viral gene expression and is essential for viral replication. The Major Capsid Protein is responsible for the formation of the viral capsid, which encases the viral genome.

The Envelope Glycoprotein M is another critical component of the virus’s envelope and is involved in viral assembly and egress. Understanding the functions and interactions of these proteins is crucial for developing effective treatments and prevention strategies for equid herpesvirus-associated diseases.

The use of recombinant proteins/cDNA in academic research and therapeutic applications has skyrocketed. However, in heterologous expression systems, successful recombinant protein expression is dependent on a variety of factors, including codon preference, RNA secondary structure, and GC content. When compared to pre-optimization, more and more experimental results demonstrated that the expression level was dramatically increased, ranging from two to hundred times depending on the gene. Bioclone has created a proprietary technology platform that has resulted in the creation of over 6,000 artificially synthesized codon-optimized cDNA clones (cloned in E. coli expression Vector), which are ready for production of the recombinant proteins.

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