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Cat# | Products | Swiss Prot# | Size | Price (US$) | Order |
PQ0091 | Recombinant Protein-Escherichia coli Cytolethal distending toxin subunit A CDT A (a.a.22 to 258) | Q46668 | 100µg | 1195 | |
PQ0092 | Recombinant Protein-Escherichia coli Cytolethal distending toxin subunit C CDT C (a.a.25 to 181) | Q46670 | 100µg | 1195 | |
PQ0093 | Recombinant Protein-Escherichia coli Heat-labile enterotoxin B subunit (a.a.34 to 104) | B8XN37 | 100µg | 1195 | |
PQ0094 | Recombinant Protein-Escherichia coli Heat-stable toxin (a.a.28 to 72) | Q2WE95 | 100µg | 1195 | |
PQ0095 | Recombinant Protein-Escherichia coli Heat-stable toxin II (a.a.21 to 159) | Q56437 | 100µg | 1195 | |
PQ0096 | Recombinant Protein-Escherichia coli Hemolysin toxin protein A (a.a.61 to 460) | A1EAA3 | 100µg | 1195 | |
PQ0097 | Recombinant Protein-Escherichia coli Shiga toxin 1 variant B subunit (a.a.26 to 89) | Q83XK2 | 100µg | 1195 | |
PQ0098 | Recombinant Protein-Escherichia coli Shiga toxin 1A subunit (a.a.1 to 305) | B3VKJ9 | 100µg | 1195 | |
PQ0099 | Recombinant Protein-Escherichia coli Shiga toxin 2 B-subunit (a.a.23 to 89) | Q9R2T5 | 100µg | 1195 | |
PQ0101 | Recombinant Protein-Escherichia coli Shiga toxin 2 variant B-subunit Stx2fB protein (a.a.22 to 87) | Q47646 | 100µg | 1195 | |
PQ0102 | Recombinant Protein-Escherichia coli Shiga toxin subunit A (a.a.41 to 215) | Q0ZHE3 | 100µg | 1195 | |
PQ0103 | Recombinant Protein-Escherichia coli Shiga-like toxin type 2 subunit A (a.a.27 to 319) | Q9FD43 | 100µg | 1195 | |
PQ0104 | Recombinant Protein-Escherichia coli Shiga-like toxin type-I alpha subunit (a.a.24 to 315) | Q47647 | 100µg | 1195 | |
PQ0105 | Recombinant Protein-Escherichia coli Toxin subunit Set1A (a.a.1 to 177) | Q7BS44 | 100µg | 1195 | |
PQ0106 | Recombinant Protein-Escherichia coli RE toxin (a.a.45 to 105) | B3XEA0 | 100µg | 1195 | |
PQ0107 | Recombinant Protein-Escherichia coli Toxin ChpA (a.a.1 to 111) | C8UAB4 | 100µg | 1195 | |
PQ0108 | Recombinant Protein-Escherichia coli Shiga toxin 2 A-subunit (a.a.25 to 319) | Q7DI68 | 100µg | 1195 | |
PQ0109 | Recombinant Protein-Escherichia coli Shiga toxin 1 B subunit (a.a.20 to 89) | Q7DH26 | 100µg | 1195 | |
PQ0110 | Recombinant Protein-Escherichia coli Toxin B (a.a.22 to 320) | O82916 | 100µg | 1195 | |
PQ0111 | Recombinant Protein-Escherichia coli Shiga toxin subunit A (a.a.1 to 260) | B2PIT5 | 100µg | 1195 | |
PQ0112 | Recombinant Protein-Escherichia coli Shiga toxin subunit A (a.a.40 to 366) | B3BQ93 | 100µg | 1195 | |
PQ0113 | Recombinant Protein-Escherichia coli Shiga toxin 1 subunit A (a.a.1 to 318) | C8TPY4 | 100µg | 1195 | |
PQ0114 | Recombinant Protein-Escherichia coli Stability protein (a.a.1 to 95) | B7LIF2 | 100µg | 1195 | |
PQ0115 | Recombinant Protein-Escherichia coli Stability protein StbE (a.a.1 to 93) | B7LIT6 | 100µg | 1195 | |
RPQ0091 | cDNA-Escherichia coli Cytolethal distending toxin subunit A CDT A (a.a.22 to 258) | Q46668 | 2µg | 1180 | |
RPQ0092 | cDNA-Escherichia coli Cytolethal distending toxin subunit C CDT C (a.a.25 to 181) | Q46670 | 2µg | 780 | |
RPQ0093 | cDNA-Escherichia coli Heat-labile enterotoxin B subunit (a.a.34 to 104) | B8XN37 | 2µg | 700 | |
RPQ0094 | cDNA-Escherichia coli Heat-stable toxin (a.a.28 to 72) | Q2WE95 | 2µg | 700 | |
RPQ0095 | cDNA-Escherichia coli Heat-stable toxin II (a.a.21 to 159) | Q56437 | 2µg | 690 | |
RPQ0096 | cDNA-Escherichia coli Hemolysin toxin protein A (a.a.61 to 460) | A1EAA3 | 2µg | 1995 | |
RPQ0097 | cDNA-Escherichia coli Shiga toxin 1 variant B subunit (a.a.26 to 89) | Q83XK2 | 2µg | 700 | |
RPQ0098 | cDNA-Escherichia coli Shiga toxin 1A subunit (a.a.1 to 305) | B3VKJ9 | 2µg | 1520 | |
RPQ0099 | cDNA-Escherichia coli Shiga toxin 2 B-subunit (a.a.23 to 89) | Q9R2T5 | 2µg | 700 | |
RPQ0101 | cDNA-Escherichia coli Shiga toxin 2 variant B-subunit Stx2fB protein (a.a.22 to 87) | Q47646 | 2µg | 700 | |
RPQ0102 | cDNA-Escherichia coli Shiga toxin subunit A (a.a.41 to 215) | Q0ZHE3 | 2µg | 870 | |
RPQ0103 | cDNA-Escherichia coli Shiga-like toxin type 2 subunit A (a.a.27 to 319) | Q9FD43 | 2µg | 1460 | |
RPQ0104 | cDNA-Escherichia coli Shiga-like toxin type-I alpha subunit (a.a.24 to 315) | Q47647 | 2µg | 1455 | |
RPQ0105 | cDNA-Escherichia coli Toxin subunit Set1A (a.a.1 to 177) | Q7BS44 | 2µg | 880 | |
RPQ0106 | cDNA-Escherichia coli RE toxin (a.a.45 to 105) | B3XEA0 | 2µg | 700 | |
RPQ0107 | cDNA-Escherichia coli Toxin ChpA (a.a.1 to 111) | C8UAB4 | 2µg | 700 | |
RPQ0108 | cDNA-Escherichia coli Shiga toxin 2 A-subunit (a.a.25 to 319) | Q7DI68 | 2µg | 1470 | |
RPQ0109 | cDNA-Escherichia coli Shiga toxin 1 B subunit (a.a.20 to 89) | Q7DH26 | 2µg | 700 | |
RPQ0110 | cDNA-Escherichia coli Toxin B (a.a.22 to 320) | O82916 | 2µg | 1490 | |
RPQ0111 | cDNA-Escherichia coli Shiga toxin subunit A (a.a.1 to 260) | B2PIT5 | 2µg | 1295 | |
RPQ0112 | cDNA-Escherichia coli Shiga toxin subunit A (a.a.40 to 366) | B3BQ93 | 2µg | 1630 | |
RPQ0113 | cDNA-Escherichia coli Shiga toxin 1 subunit A (a.a.1 to 318) | C8TPY4 | 2µg | 1585 | |
RPQ0114 | cDNA-Escherichia coli Stability protein (a.a.1 to 95) | B7LIF2 | 2µg | 700 | |
RPQ0115 | cDNA-Escherichia coli Stability protein StbE (a.a.1 to 93) | B7LIT6 | 2µg | 700 |
Escherichia coli cDNA and recombinant antigen
Escherichia coli (E. coli) is a common bacterium that is found in the gut of humans and animals. While most strains of E. coli are harmless, some can cause severe illness, especially in people with weakened immune systems. One of the key factors that contribute to the pathogenicity of E. coli is the production of various toxins, including Shiga, heat-labile, heat-stable, and cytolethal distending toxins.
Shiga toxins, also known as verotoxins, are a group of toxins produced by some strains of E. coli that can cause damage to the kidneys, leading to hemolytic uremic syndrome (HUS). These toxins are composed of two subunits, A and B, with subunit A responsible for the toxic effects. Shiga toxins are a major cause of foodborne illness, especially in outbreaks associated with undercooked ground beef.
Heat-labile enterotoxin and heat-stable enterotoxins are produced by some strains of E. coli that cause gastroenteritis. These toxins can cause diarrhea and vomiting by disrupting the normal function of the intestines. The heat-labile enterotoxin is composed of two subunits, A and B, while the heat-stable enterotoxins are small peptides.
Cytolethal distending toxins (CDTs) are produced by some strains of E. coli that can cause cell cycle arrest and cell death in host cells. These toxins are composed of three subunits, A, B, and C, with subunit A responsible for the toxic effects. CDTs can contribute to the severity of E. coli infections by damaging the intestinal lining and other tissues.
In addition to these toxins, E. coli also produces other toxins, such as hemolysin, RE toxin, ChpA toxin, and Set1A toxin, which can cause tissue damage and contribute to the pathogenesis of the bacterium.
Understanding the mechanisms and effects of these toxins is essential for the development of effective treatments for E. coli infections. Researchers are exploring various approaches to target these toxins, including vaccines and therapies that can neutralize the toxins or prevent their production.
In summary, E. coli is a bacterium that can cause a range of illnesses in humans, and the production of various toxins, including Shiga, heat-labile, heat-stable, and cytolethal distending toxins, is a key factor in the pathogenesis of the bacterium. Ongoing research is focused on developing effective treatments to target these toxins and improve outcomes for people with E. coli infections.
The use of recombinant proteins/cDNA in academic research and therapeutic applications has skyrocketed. However, successful recombinant protein expression in heterologous expression systems depends on various factors, including codon preference, RNA secondary structure, and GC content. 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. Compared to pre-optimization, more experimental results demonstrated that the expression level was dramatically increased, ranging from two to a hundred times depending on the gene.
Escherichia coli cDNA and recombinant antigen microarrays are powerful tools for the identification of novel bacterial virulence targets. Microarrays can be used to identify differentially expressed genes in different bacterial strains, and to compare the expression profiles of different bacterial strains. This can be used to identify novel virulence targets that may not have been previously identified. Additionally, using recombinant antigens, microarrays can be used to identify new virulence-associated proteins that may be involved in pathogenesis. These targets can then be used to develop novel vaccines and drugs to combat bacterial infections.
The Escherichia coli genome is a circular DNA molecule of approximately 4.6 million base pairs. It encodes 4,288 genes, including many involved in the metabolism and transport of carbohydrates, amino acids, nucleotides, proteins, and other nutrients. It also contains genes involved in DNA replication and repair, transcription, translation, and cell cycle control. The E. coli genome also includes several mobile genetic elements, including plasmids, transposons, and integrons, which can be exchanged among bacteria and can facilitate the acquisition of new genes.
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