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Cat# | Product Name | Swiss Prot# | Size | Price (US$) | Order |
PN0356 | Recombinant Protein-Epstein-Barr virus Epstein-Barr nuclear antigen 3 (a.a.50 to 450) | Q69138 | 100 µg | 1195 | |
PN0357 | Recombinant Protein-Epstein-Barr virus Epstein-Barr nuclear antigen 4 (a.a.50 to 450) | Q1HVG4 | 100 µg | 1195 | |
PN0358 | Recombinant Protein-Epstein-Barr virus Epstein-Barr nuclear antigen 6 (a.a.391 to 976) | Q69140 | 100 µg | 1195 | |
PN0359 | Recombinant Protein-Epstein-Barr virus Envelope glycoprotein B GP115 (a.a.23 to 450) | P0C763 | 100 µg | 1195 | |
PN0360 | Recombinant Protein-Epstein-Barr virus Envelope glycoprotein H gp85 (a.a.19 to 450) | Q1HVD2 | 100 µg | 1195 | |
PN0361 | Recombinant Protein-Epstein-Barr virus Envelope glycoprotein L gp25 (a.a.23 to 137) | Q1HVF6 | 100 µg | 1195 | |
PN0362 | Recombinant Protein-Epstein-Barr virus Glycoprotein 42 gp42 (a.a.30 to 223) | Q1HVG2 | 100 µg | 1195 | |
PN0363 | Recombinant Protein-Epstein-Barr virus Major capsid protein (a.a.50 to 450) | P0C703 | 100 µg | 1195 | |
PN0364 | Recombinant Protein-Epstein-Barr virus Envelope glycoprotein GP340 (a.a.50 to 450) | P68343 | 100 µg | 1195 | |
PN0365 | Recombinant Protein-Epstein-Barr virus Glycoprotein 42 gp42 (a.a.30 to 223) | P03205 | 100 µg | 1195 | |
PN0366 | Recombinant Protein-Epstein-Barr virus Latent membrane protein 1 (a.a.242 to 386) | P03230 | 100 µg | 1195 | |
PN0367 | Recombinant Protein-Epstein-Barr virus Envelope glycoprotein GP340/GP220 (a.a.502 to 698) | P03200 | 100 µg | 1195 | |
PN0368 | Recombinant Protein-Epstein-Barr virus Probable capsid protein VP23 (Protein BDLF1) (a.a.39 to 301) | P25214 | 100 µg | 1195 | |
PN0369 | Recombinant Protein-Epstein-Barr virus Capsid protein VP26 (a.a.21 to 176) | P14348 | 100 µg | 1195 | |
PN0370 | Recombinant Protein-Epstein-Barr virus Apoptosis regulator BHRF1-Early antigen protein R (a.a.37 to 191) | P0C736 | 100 µg | 1195 | |
PN0371 | Recombinant Protein-Epstein-Barr virus-EBV nuclear antigen 2-EBNA-2(a.a.1 to 176) | Q3KSV2 | 100 µg | 1195 | |
PN0372 | Recombinant Protein-Epstein-Barr virus nuclear antigen EBNA-3B (a.a.50 to 450) | Q69139 | 100 µg | 1195 | |
RPN0356 | cDNA-Epstein-Barr virus Epstein-Barr nuclear antigen 3 (a.a.50 to 450) | Q69138 | 2 µg | 2000 | |
RPN0357 | cDNA-Epstein-Barr virus Epstein-Barr nuclear antigen 4 (a.a.50 to 450) | Q1HVG4 | 2 µg | 2000 | |
RPN0358 | cDNA-Epstein-Barr virus Epstein-Barr nuclear antigen 6 (a.a.391 to 976) | Q69140 | 2 µg | 2925 | |
RPN0359 | cDNA-Epstein-Barr virus Envelope glycoprotein B GP115 (a.a.23 to 450) | P0C763 | 2 µg | 2135 | |
RPN0360 | cDNA-Epstein-Barr virus Envelope glycoprotein H gp85 (a.a.19 to 450) | Q1HVD2 | 2 µg | 2155 | |
RPN0361 | cDNA-Epstein-Barr virus Envelope glycoprotein L gp25 (a.a.23 to 137) | Q1HVF6 | 2 µg | 800 | |
RPN0362 | cDNA-Epstein-Barr virus Glycoprotein 42 gp42 (a.a.30 to 223) | Q1HVG2 | 2 µg | 965 | |
RPN0363 | cDNA-Epstein-Barr virus Major capsid protein (a.a.50 to 450) | P0C703 | 2 µg | 2000 | |
RPN0364 | cDNA-Epstein-Barr virus Envelope glycoprotein GP340 (a.a.50 to 450) | P68343 | 2 µg | 2000 | |
RPN0365 | cDNA-Epstein-Barr virus Glycoprotein 42 gp42 (a.a.30 to 223) | P03205 | 2 µg | 965 | |
RPN0366 | cDNA-Epstein-Barr virus Latent membrane protein 1 (a.a.242 to 386) | P03230 | 2 µg | 720 | |
RPN0367 | cDNA-Epstein-Barr virus Envelope glycoprotein GP340/GP220 (a.a.502 to 698) | P03200 | 2 µg | 980 | |
RPN0368 | cDNA-Epstein-Barr virus Probable capsid protein VP23 (Protein BDLF1) (a.a.39 to 301) | P25214 | 2 µg | 1310 | |
RPN0369 | cDNA-Epstein-Barr virus Capsid protein VP26 (a.a.21 to 176) | P14348 | 2 µg | 775 | |
RPN0370 | cDNA-Epstein-Barr virus Apoptosis regulator BHRF1-Early antigen protein R (a.a.37 to 191) | P0C736 | 2 µg | 770 | |
RPN0371 | cDNA-Epstein-Barr virus-EBV nuclear antigen 2-EBNA-2(a.a.1 to 176) | Q3KSV2 | 2 µg | 875 | |
RPN0372 | cDNA-Epstein-Barr virus nuclear antigen EBNA-3B (a.a.50 to 450) | Q69139 | 2 µg | 2000 |
Epstein-Barr virus cDNA and recombinant antigen
The EBV genome has been fully sequenced, and it has been found that it is highly variable among different strains of the virus. The variability in the genome is responsible for the diversity in viral antigenicity and pathogenicity. The virus genome encodes many proteins, including:
Barr nuclear antigen 3 (EBNA-3): This is a family of nuclear proteins that play a role in regulating the expression of viral and host genes.
Barr nuclear antigen 4 (EBNA-4): This is another nuclear protein that is involved in regulating gene expression.
Barr nuclear antigen 6 (EBNA-6): This is a family of nuclear proteins that are involved in regulating the replication and maintenance of the viral genome.
B GP115: This is a glycoprotein that is involved in viral entry and infectivity.
H gp85 and L gp25: These are glycoproteins that form the viral envelope and are involved in viral entry.
GP42: This is a glycoprotein that binds to host cells and facilitates viral entry.
Major capsid protein: This is a structural protein that forms the outer shell of the virus.
GP340: This is a glycoprotein that binds to host cells and facilitates viral entry.
Latent membrane protein 1 (LMP1): This is a membrane protein that is involved in promoting cell survival and proliferation.
VP23 and VP26: These are structural proteins that form the inner shell of the virus.
BHRF1: This is a viral protein that is involved in inhibiting apoptosis and promoting viral replication.
EBNA-2: This is a nuclear protein that is involved in regulating the expression of viral and host genes.
EBNA-3B: This is a nuclear protein that is involved in regulating gene expression and inhibiting apoptosis.
Many of these proteins are involved in viral replication, viral entry, and modulation of host cell functions to promote viral persistence. Some of these proteins also play a role in the pathogenesis of EBV-associated diseases.
Understanding the functions and interactions of these proteins is crucial for developing effective treatments and prevention strategies for EBV-associated diseases. Ongoing research is focused on uncovering more about the virus and its proteins, with the goal of ultimately finding a way to control and eradicate the disease.
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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