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| Product | Description | |
|---|---|---|
| Cbz-Ser(tBu)-Ser(tBu)-Gly-OH | Cbz-Ser(tBu)-Ser(tBu)-Gly-OH is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the serine (Ser) residue, preventing it from participating in unwanted reactions during synthesis. The hydroxyl groups on both serine residues are protected by tBu (tert-butyl) groups, which keep these groups from reacting until they are selectively deprotected. Gly (Glycine) is the final amino acid in the sequence, and the -OH at the C-terminus indicates a free carboxyl group. This free carboxyl group allows for further peptide coupling or modification. This compound is used to incorporate serine and glycine into peptides while maintaining control over the reactivity of functional groups through specific protection strategies. Alternative Names: SSG; Cbz-Ser(OtBu)-Ser(OtBu)-Gly-OH; Z-Ser(tBu)-Ser(tBu)-Gly-OH; N-(N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-seryl)-O-(tert-butyl)-L-serylglycine. Grades: ≥95%. Molecular formula: C24H37N3O8. Mole weight: 495.57. |  |
| Cbz-Ser(tBu)-Ser(tBu)-Gly-OMe | Cbz-Ser(tBu)-Ser(tBu)-Gly-OMe is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the serine (Ser) residue, preventing it from reacting during synthesis. The hydroxyl groups on both serine residues are protected by tBu (tert-butyl) groups, which shield these groups from reactivity until they are selectively deprotected. Gly (Glycine), the final amino acid in the sequence, is the smallest and most flexible amino acid, with the OMe (methyl ester) at the C-terminus indicating that the carboxyl group of glycine is esterified. This esterification is useful for controlling reactivity or facilitating further modifications. This compound is used to introduce serine and glycine into peptides while maintaining precise control over functional group reactivity through selective protection. Alternative Names: SSG; Methyl N-(N-((benzyloxy)carbonyl)-O-(tert-butyl)-L-seryl)-O-(tert-butyl)-L-serylglycinate; Z-Ser(tBu)-Ser(tBu)-Gly-OMe; Cbz-Ser(OtBu)-Ser(OtBu)-Gly-OMe. Grades: ≥95%. Molecular formula: C25H39N3O8. Mole weight: 509.60. | |
| Cbz-Ser(tBu)-Ser(tBu)-OH | Cbz-Ser(tBu)-Ser(tBu)-OH is a protected dipeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group serves as a protective group for the N-terminus of the first serine residue, preventing unwanted reactions during the synthesis process. Each Ser (Serine) residue is protected at its hydroxyl side chain by a tBu (tert-butyl) group, ensuring that these reactive groups remain unaltered until selective deprotection is required. The -OH at the C-terminus indicates a free carboxyl group, allowing for further coupling reactions in the peptide chain. This compound is used to incorporate serine residues into peptides, with specific protections to facilitate precise and controlled synthesis. Alternative Names: N-(N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-seryl)-O-(tert-butyl)-L-serine; N-Benzoxycarbonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serine; SS; Cbz-Ser(OtBu)-Ser(OtBu)-OH; Z-Ser(tBu)-Ser(tBu)-OH. Grades: ≥95%. CAS No. 119439-59-7. Molecular formula: C22H34N2O7. Mole weight: 438.51. | |
| Cbz-Thr(OtBu)-Phe-Thr(OtBu)-OMe | Cbz-Thr(OtBu)-Phe-Thr(OtBu)-OMe is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the threonine (Thr) residue, preventing it from participating in unwanted reactions. The hydroxyl groups on both threonine residues are protected by OtBu (tert-butyl) groups, ensuring these functional groups remain unreactive until selective deprotection is required. Phe (Phenylalanine), positioned in the middle, adds aromatic and hydrophobic properties to the peptide. The OMe (methyl ester) at the C-terminus indicates that the carboxyl group of the final threonine is esterified, which can facilitate further reactions or modifications. This compound is used to incorporate threonine and phenylalanine into peptides, with controlled reactivity through selective protection, enabling precise and efficient peptide synthesis. Alternative Names: TFT; Cbz-Thr(tBu)-Phe-Thr(tBu)-OMe; Z-Thr(OtBu)-Phe-Thr(OtBu)-OMe; Methyl N-N-((benzyloxy)carbonyl)-O-(tert-butyl)-L-threonyl-L-phenylalanyl-O-(tert-butyl)-L-threoninate. Grades: ≥95%. Molecular formula: C34H49N3O8. Mole weight: 627.78. | |
| Cbz-Thr-Phe-Thr(tBu)-OMe | Cbz-Thr-Phe-Thr(tBu)-OMe is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the first threonine (Thr) residue, preventing it from participating in unwanted reactions during the synthesis process. The side chain of the second threonine residue is protected by a tBu (tert-butyl) group, shielding the hydroxyl group from reactivity until selective deprotection is needed. Phe (Phenylalanine), the middle amino acid, contributes aromatic and hydrophobic properties to the peptide sequence. The OMe (methyl ester) at the C-terminus indicates that the carboxyl group of the second threonine is esterified, which is useful for controlling the reactivity and allowing further modifications or elongation of the peptide chain. This compound is employed to introduce threonine and phenylalanine into peptides, with specific protections to ensure selective and controlled synthesis. Alternative Names: TFT; Methyl N-((benzyloxy)carbonyl)-L-threonyl-L-phenylalanyl-O-(tert-butyl)-L-threoninate; Z-Thr-Phe-Thr(tBu)-OMe. Grades: ≥95%. Molecular formula: C30H41N3O8. Mole weight: 571.67. | |
| Cbz-Thr(tBu)-Phe-OH | Cbz-Thr(tBu)-Phe-OH is a protected dipeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the threonine residue, preventing reactions at this site during synthesis. The Thr (Threonine) residue is further protected at its hydroxyl side chain by a tBu (tert-butyl) group, ensuring the hydroxyl group remains unreactive until deprotection is desired. Phe (Phenylalanine) is the second amino acid, contributing aromatic character to the peptide. The -OH at the C-terminus signifies a free carboxyl group, which can participate in peptide bond formation. This compound is used to introduce threonine and phenylalanine into peptides with specific protective measures for controlled and selective synthesis. Alternative Names: N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-threonyl-L-phenylalanine; Z-Thr(tBu)-Phe-OH; N-Benzoxycarbonyl-O3-tert-butyl-L-threonyl-L-phenylalanine; TF; L-Phenylalanine, N-[O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-L-threonyl]-. Grades: ≥95%. CAS No. 47732-07-0. Molecular formula: C25H32N2O6. Mole weight: 456.54. | |
| Cbz-Thr(tBu)-Phe-Thr(tBu)-OH | Cbz-Thr(tBu)-Phe-Thr(tBu)-OH is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the threonine (Thr) residue, preventing it from reacting during synthesis. Both threonine residues have their side chain hydroxyl groups protected by tBu (tert-butyl) groups, which shield these groups from unwanted reactions until deprotection is desired. Phe (Phenylalanine), the central amino acid in the sequence, adds aromatic and hydrophobic properties to the peptide. The -OH at the C-terminus indicates a free carboxyl group, allowing for further peptide coupling. This compound is used to incorporate threonine and phenylalanine into peptides while maintaining control over the functional groups' reactivity through selective protection. Alternative Names: TFT; N-N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-threonyl-L-phenylalanyl-O-(tert-butyl)-L-threonine; Z-Thr(tBu)-Phe-Thr(tBu)-OH; Cbz-Thr(OtBu)-Phe-Thr(OtBu)-OH. Grades: ≥95%. Molecular formula: C33H47N3O8. Mole weight: 613.75. | |
| Cbz-Tyr(OtBu)-Ser(OtBu)-OMe | Cbz-Tyr(OtBu)-Ser(OtBu)-OMe is a protected dipeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the tyrosine (Tyr) residue, preventing it from reacting during synthesis. The hydroxyl group of tyrosine is protected by an OtBu (tert-butyl) group, ensuring it remains unreactive until deprotection is necessary. The Ser (Serine) residue is similarly protected at its hydroxyl group by an OtBu group. The OMe (methyl ester) at the C-terminus indicates that the carboxyl group of the serine is esterified, facilitating further peptide coupling or modification. This compound is used to introduce tyrosine and serine into peptides while controlling the reactivity of their functional groups. Alternative Names: Z-Tyr(OtBu)-Ser(OtBu)-OMe; Methyl N-((S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoyl)-O-(tert-butyl)-L-serinate; YS. Grades: ≥95%. Molecular formula: C29H40N2O7. Mole weight: 528.65. | |
| C(Cbz)-acetic acid | C(Cbz)-acetic acid. Alternative Names: 2-Oxo-4-[(benzyloxycarbonyl)amino]pyrimidine-1(2H)-acetic acid. CAS No. 144564-95-4. Molecular formula: C14H13N3O5. Mole weight: 303.27. | |
| Cc-CATH2 | Cc-CATH2 is isolated from Coturnix coturnix. Cc-CATH2 showed considerable reduction of cytotoxic activity compared to other avian cathelicidins, with average IC(50) values of 20.18μm. | |
| Cc-CATH3 | Cc-CATH3 is isolated from Coturnix coturnix. Cc-CATH3 is an avian antimicrobial peptide (AMP) with 29 amino acids in length containing a broad-spectrum antibacterial activity. Cc-CATH3 showed considerable reduction of cytotoxic activity compared to other avian cathelicidins, with average IC(50) values of 17.16 μm. | |
| CcD1 | CcD1 is isolated from Capsicum chinense. It has antifungal activity. | |
| Cc-GRP | Cc-GRP is a peptide with a molecular weight of 7kDa and it was observed to display homology to GRPs. Cc-GRP has antifungal activity. | |
| CCHa2 | CCHa2. Alternative Names: H-Gly-Cys-Gln-Ala-Tyr-Gly-His-Val-Cys-Tyr-Gly-Gly-His-NH2. Molecular formula: C57H79N19O16S2. Mole weight: 1350.48. | |
| CCK-4 Acetate | Tetragastrin is a tetrapeptide. Alternative Names: CCK-4; CCK4; CCK 4; Gastrin Tetrapeptide; Cholecystokinin Octapeptide (5-8); Cholecystokinin Tetrapeptide; Gastrin (14-17) (human). CAS No. 35144-91-3. Molecular formula: C29H36N6O6S. Mole weight: 596.70. | |
| CCK Octapeptide (non-sulfated) | Cholecystokinin (CCK) is a neuropeptide and gut hormone that regulates pancreatic enzyme secretion and gastrointestinal motility, and acts as a satiety signal. CCK Octapeptide (non-sulfated) is the non-sulfated form of the C-terminal octapeptide of CCK. Alternative Names: CCK-8 (desulfated); Cholecystokinin (CCK) (26-33); 2-desulfo-cholecystokinin-8 (swine). Grades: 98%. CAS No. 25679-24-7. Molecular formula: C49H62N10O13S2. Mole weight: 1063. | |
| CCL27 | CCL27 is a chemotactic factor that attracts skin-associated memory T-lymphocytes. It may play a role in mediating homing of lymphocytes to cutaneous sites. Alternative Names: C-C Motif Chemokine Ligand 27. | |
| Cc-LTP1 | Cc-LTP1 is produced by Coffea canephora. It has active antifungal activity against Candida albicans. | |
| CCMV Gag-(7-25) | It is a cell penetrating peptide. Alternative Names: H-Lys-Leu-Thr-Arg-Ala-Gln-Arg-Arg-Ala-Ala-Ala-Arg-Lys-Asn-Lys-Arg-Asn-Thr-Arg-OH; L-lysyl-L-leucyl-L-threonyl-L-arginyl-L-alanyl-L-glutaminyl-L-arginyl-L-arginyl-L-alanyl-L-alanyl-L-alanyl-L-arginyl-L-lysyl-L-asparagyl-L-lysyl-L-arginyl-L-asparagyl-L-threonyl-L-arginine. Grades: ≥95%. Molecular formula: C93H175N43O25. Mole weight: 2295.70. | |
| C-Cys-Mel | C-Cys-Mel. Alternative Names: Gly-Ile-Gly-Ala-Val-Leu-Lys-Val-Leu-Thr-Thr-Gly-Leu-Pro-Ala-Leu-Ile-Ser-Trp-Ile-Lys-Arg-Lys-Arg-Gln-Gln-Cys. | |
| CD20 (188-196) | CD20 (188-196) is a truncated fragment of a membrane phosphoprotein, CD20, which is expressed on the surface of B cells. CD20 receptor is an important target for immunotherapy against B cell lymphoma. Alternative Names: B-lymphocyte antigen CD20 (188-196). Grades: >95%. Molecular formula: C46H77N9O12. Mole weight: 948.16. | |
| CD59 glycoprotein precursor (106-114) | CD59 glycoprotein precursor (106-114) is a peptide derived from CD59 glycoprotein precursor which is a potent inhibitor of the complement membrane attack complex (MAC) action. CD59 glycoprotein is involved in signal transduction for T-cell activation complexed to a protein tyrosine kinase. Alternative Names: HRF-20 (106-114); Membrane attack complex inhibition factor (106-114). | |
| Cdc25A (80-93) (human) | Cdc25A abundance fluctuates periodically during the cell division cycle and is mainly regulated by the ubiquitin-proteasome system, through the action of two ubiquitin ligase complexes, which later promote complex / cyclosome and Skp1/Cul1/F-box proteins. Due to the presence of the destruction motif (KEN-box) in Cdc25A, ubiquitination and degradation occur at the mitotic outlet and G1, while phosphorylation events modulate the stability of Cdc25A protein in the S phase, both in undisturbed cells and in cells exposed to DNA damage agents or DNA replication inhibitors. Alternative Names: H-Thr-Asp-Ser-Gly-Phe-Cys-Leu-Asp-Ser-Pro-Gly-Pro-Leu-Asp-OH. Grades: ≥95%. CAS No. 851538-67-5. Molecular formula: C60H90N14O24S. Mole weight: 1423.52. | |
| CDK2 | CDK2, a member of the eukaryotic S/T protein kinase family, catalyzes the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S0/T0) in a protein substrate. Activity of CDK2 is maximal during S phase and G2; activated by interaction with cyclin E during the early stages of DNA synthesis to permit G1-S transition, and subsequently activated by cyclin A2 (cyclin A1 in germ cells) during the late stages of DNA replication to drive the transition from S phase to mitosis, the G2 phase. Alternative Names: Cell division protein kinase 2; kinase Cdk2; p33 protein kinase; Anti-Gastric receptor I; Anti-H2R; His-His-Ala-Ser-Pro-Arg-Lys; L-histidyl-L-histidyl-L-alanyl-L-seryl-L-prolyl-L-arginyl-L-lysine. Grades: ≥95%. CAS No. 255064-79-0. Molecular formula: C35H57N15O9. Mole weight: 831.92. | |
| CDK2 acetate | CDK2 acetate, a member of the eukaryotic S/T protein kinase family, catalyzes the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S0/T0) in a protein substrate. Alternative Names: H-His-His-Ala-Ser-Pro-Arg-Lys-OH.CH3CO2H; L-histidyl-L-histidyl-L-alanyl-L-seryl-L-prolyl-L-arginyl-L-lysine acetic acid. Grades: ≥95%. Molecular formula: C37H61N15O11. Mole weight: 891.99. | |
| CDK4-R24C (23-32) | CDK4-R24C (23-32) is a peptide derived from CDK4-R24C. The common mutation in CDK4 (CDK4R24C) in melanoma inhibits the interaction with p16INK4A and thus leads to constitutive activation. | |
| CEC1_DROVI Cecropin-1 precursor | CEC1_DROVI Cecropin-1 precursor has antibacterial activity. The source of CEC1_DROVI Cecropin-1 precursor is Drosophila virilis. Grades: >95% by HPLC. Molecular formula: C182H311N61O51. Mole weight: 4169.78. | |
| CEC3_DROVI Cecropin-3 precursor | CEC3_DROVI Cecropin-3 precursor was found in Drosophila virilis. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CEC4_BOMMO Cecropin | CEC4_BOMMO Cecropin has antibacterial activity. CEC4_BOMMO Cecropin was found in Bombyx mori. Grades: >97% by HPLC. Molecular formula: C172H291N51O43. Mole weight: 3761.46. | |
| CECA1_DROSI Cecropin-A1 precursor | CECA1_DROSI Cecropin-A1 precursor was found in Drosophila simulans. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CECC_DROTK Cecropin-C precursor | CECC_DROTK Cecropin-C precursor was found in Drosophila takahashii. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CECD_BOMMO Cecropin-D precursor | CECD_BOMMO Cecropin-D precursor was found in Bombyx mori. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CECE_BOMMO Antibacterial peptide enbocin precursor | CECE_BOMMO Antibacterial peptide enbocin precursor was found in Bombyx mori. It has antibacterial activity against Gram-positive and Gram-negative bacteria. | |
| Cecropin | Cecropin was found in Oiketicus kirbyi. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-1 | Cecropin-1 was found in Ceratitis capitata. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-2 | Cecropin-2 was found in Ceratitis capitata. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-A | Cecropin-A was found in Culex pipiens pipiens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin A1 | Cecropin A1 was found in Bombyx mori. It has antibacterial activity. | |
| Cecropin-A1 | Cecropin-A1 was found in Drosophila mauritiana. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-A2 | Cecropin-A2 was found in Aedes albopictus. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. Alternative Names: H-Gly-Gly-Leu-Lys-Lys-Phe-Gly-Lys-Lys-Leu-Glu-Gly-Val-Gly-Lys-Arg-Val-Phe-Lys-Ala-Ser-Glu-Lys-Ala-Leu-Pro-Val-Ala-Val-Gly-Ile-Lys-Ala-Leu-Gly-Lys-OH. Grades: >97% by HPLC. Molecular formula: C172H298N48O42. Mole weight: 3710.49. | |
| Cecropin-A precursor | Cecropin-A precursor was found in Anopheles gambiae. It has antibacterial activity against several Gram-positive and Gram-negative bacteria. It also has antifungal activity against A.fumigatus, B.cinerea, F.culmorum, F.oxysporum, N.crassa, C.albicans, C.neoformans and S.cerevisiae. | |
| Cecropin-B | Cecropin-B was found in Heliothis virescens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. It also has activity against fungi. | |
| Cecropin B1 | Cecropin B1 was found in Bombyx mori. It has antibacterial activity. | |
| Cecropin-B1 | Cecropin-B1 was found in Culex pipiens pipiens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-B2 | Cecropin-B2 was found in Culex pipiens pipiens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin B (free acid) | Cecropin B (free acid). Alternative Names: Cecropin B, free acid; H-Lys-Trp-Lys-Val-Phe-Lys-Lys-Ile-Glu-Lys-Met-Gly-Arg-Asn-Ile-Arg-Asn-Gly-Ile-Val-Lys-Ala-Gly-Pro-Ala-Ile-Ala-Val-Leu-Gly-Glu-Ala-Lys-Ala-Leu-OH. Grades: ≥95%. CAS No. 203265-23-0. Molecular formula: C176H301N51O42S. Mole weight: 3835.71. | |
| Cecropin B TFA salt | Cecropin B is an antibacterial peptide originally isolated from insects. It has broad-spectrum antiparasitic and antibacterial activities and is also effective against fungi. Alternative Names: P9B Protein. Grades: ≥97% by HPLC. Molecular formula: C176H302N52O41S (free base). Mole weight: 3835 (free base). | |
| Cecropin-C | Cecropin-C was found in Heliothis virescens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. It also has activity against fungi. | |
| Cecropin-C type 1 | Cecropin-C type 1 was found in Aedes albopictus. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. Alternative Names: CECC1. | |
| Cecropin-D-like peptide | Cecropin-D-like peptide is an antibacterial peptide isolated from Galleria mellonella. It has activity against gram-positive bacteria and fungi. Alternative Names: Glu-Asn-Phe-Phe-Lys-Glu-Ile-Glu-Arg-Ala-Gly-Gln-Arg-Ile-Arg-Asp-Ala-Ile-Ile-Ser-Ala-Ala-Pro-Ala-Val-Glu-Thr-Leu-Ala-Gln-Ala-Gln-Lys-Ile-Ile-Lys-Gly-Gly-Asp. Grades: 96.7%. Molecular formula: C187H309N55O58. Mole weight: 4255.84. | |
| Cecropin-P2 | Cecropin-P2 is from Ascaris suum (Pig roundworm) (Ascaris lumbricoides). It has antibacterial activity against several Gram-positive and Gram-negative bacteria. Cecropin-P2 is weakly active against yeasts. Alternative Names: CecP2. | |
| Cecropin-P3 | Cecropin-P3 is from Ascaris suum (Pig roundworm) (Ascaris lumbricoides). It has antibacterial activity against several Gram-positive and Gram-negative bacteria. Cecropin-P3 is weakly active against yeasts. Alternative Names: CecP3. | |
| Cecropin-P4 | Cecropin-P4 is from Ascaris suum (Pig roundworm) (Ascaris lumbricoides). Recombinant CecP4 showed antimicrobial activity against both Pseudomona and E. coli, suggesting the broad spectrum of its antimicrobial activity. Alternative Names: CecP4. | |
| CEF10 Epstein-Barr Virus LMP2 (426-434) | CEF10 Epstein-Barr Virus LMP2 (426-434) is a peptide that corresponds to aa 426-434 of the LMP2 protein from the Epstein-Barr Virus. Alternative Names: H-Cys-Leu-Gly-Gly-Leu-Leu-Thr-Met-Val-OH; LMP2A (426-434); L-cysteinyl-L-leucyl-glycyl-glycyl-L-leucyl-L-leucyl-L-threonyl-L-methionyl-L-valine. CAS No. 152274-91-4. Molecular formula: C39H71N9O11S2. Mole weight: 906.16. | |
| CEF11 Epstein-Barr Virus BMLF1 (280-288) | CEF11 Epstein-Barr Virus BMLF1 (280-288) is a peptide that corresponds to aa 280-288 of the BMLF1 protein from the Epstein-Barr Virus. Alternative Names: Gly-Leu-Cys-Thr-Leu-Val-Ala-Met-Leu; H-Gly-Leu-Cys-Thr-Leu-Val-Ala-Met-Leu-OH. CAS No. 183719-29-1. Molecular formula: C40H73N9O11S2. Mole weight: 920.19. | |
| CEF14, EBV Rta Protein 28-37 | It is the HLA A24 restriction epitope of Epstein-Barr virus Rta protein (28-37). Alternative Names: Asp-Tyr-Cys-Asn-Val-Leu-Asn-Lys-Glu-Phe; (3S,6S,9R,12S,15S,18S,21S,24S,27S)-3-Amino-24-(4-aminobutyl)-27-[{[(1S)-1-carboxy-2-phenylethyl]imino}(hydroxy)methyl]-4,7,10,13,16,19,22,25-octahydroxy-6-(4-hydroxybenzyl)-12,21-bis(2-hydroxy-2-iminoethyl)-18-isobutyl-15-isopropyl-9-(sulfanylmethyl)-5,8,11,14,17,20,23,26-octaazatriaconta-4,7,10,13,16,19,22,25-octaene-1,30-dioic acid. Grades: ≥95%. CAS No. 216862-58-7. Molecular formula: C55H81N13O18S. Mole weight: 1244.37. | |
| CEF19, Epstein-Barr Virus latent NA-3A 458-466 | It is a single peptide epitope representing the 458-466 residues of Epstein-Barr virus type 1 nuclear antigen 3A protein (B95.8 strain) that significantly affects cytotoxic T lymphocyte (CTL) recognition. Alternative Names: L-tyrosyl-L-prolyl-L-leucyl-L-histidyl-L-alpha-glutamyl-L-glutaminyl-L-histidyl-glycyl-L-methionine; Tyr-Pro-Leu-His-Glu-Gln-His-Gly-Met; N-{(5S,8S,11S,14S,17S)-11-(2-Carboxyethyl)-1,4,7,10,13,16,19-heptahydroxy-8-(3-hydroxy-3-iminopropyl)-5,14-bis(1H-imidazol-5-ylmethyl)-17-isobutyl-19-[(2S)-1-(L-tyrosyl)-2-pyrrolidinyl]-3,6,9,12,15,18-hexaazanonadeca-3,6,9,12,15,18-hexaen-1-ylidene}-L-methionine. Grades: ≥95%. CAS No. 157876-41-0. Molecular formula: C49H70N14O14S. Mole weight: 1111.23. | |
| CEF20 | CEF20 is the HLA-A*0201-restricted epitope from cytomegalovirus pp65 (495-503). Alternative Names: Asn-Leu-Val-Pro-Met-Val-Ala-Thr-Val; L-asparagyl-L-leucyl-L-valyl-L-prolyl-L-methionyl-L-valyl-L-alanyl-L-threonyl-L-valine; Human CMV pp65 (495-503); CEF20, Cytomegalovirus. Grades: ≥95%. CAS No. 153045-21-7. Molecular formula: C42H74N10O12S. Mole weight: 943.16. | |
| CEF20 acetate | CEF20 acetate, a CEF control peptide pool, is the HLA-A*0201-restricted epitope from cytomegalovirus pp65 (495-503). Alternative Names: H-Asn-Leu-Val-Pro-Met-Val-Ala-Thr-Val-OH.CH3CO2H; L-asparagyl-L-leucyl-L-valyl-L-prolyl-L-methionyl-L-valyl-L-alanyl-L-threonyl-L-valine acetic acid. Grades: ≥95%. Molecular formula: C44H78N10O14S. Mole weight: 1003.22. | |
| CEF25 Influenza Virus NP (44-52) | CEF25 Influenza Virus NP (44-52) is a peptide that corresponds to aa 44-52 of Influenza A virus nucleoprotein. NP is a critical component of the viral ribonucleoproteins (vRNP) complex, and the recognized functions of NP include, but are not limited to, organization of RNA packing, nuclear trafficking, and vRNA transcription and replication. Alternative Names: H-Cys-Thr-Glu-Leu-Lys-Leu-Ser-Asp-Tyr-OH; L-cysteinyl-L-threonyl-L-alpha-glutamyl-L-leucyl-L-lysyl-L-leucyl-L-seryl-L-alpha-aspartyl-L-tyrosine. CAS No. 152647-27-3. Molecular formula: C46H74N10O17S. Mole weight: 1071.20. | |
| CEF26 Influenza Virus NP (265-274) | CEF26 Influenza Virus NP (265-274) is a peptide that corresponds to aa 265-274 of Influenza A virus nucleoprotein. NP is a critical component of the viral ribonucleoproteins (vRNP) complex, and the recognized functions of NP include, but are not limited to, organization of RNA packing, nuclear trafficking, and vRNA transcription and replication. Alternative Names: H-Ile-Leu-Arg-Gly-Ser-Val-Ala-His-Lys-OH; Ile-Leu-Arg-Gly-Ser-Val-Ala-His-Lys. Molecular formula: C43H77N15O11. Mole weight: 980.23. | |
| CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 | It is the 148-156 amino acid fragment of the BRLF1 protein. BRLF1 is a transcriptional activator that directly binds to GC-rich motif in the promoter of EBV lytic gene. Alternative Names: L-Lysine, L-arginyl-L-valyl-L-arginyl-L-alanyl-L-tyrosyl-L-threonyl-L-tyrosyl-L-seryl-; Arg-Val-Arg-Ala-Tyr-Thr-Tyr-Ser-Lys. Grades: ≥95%. CAS No. 254110-79-7. Molecular formula: C51H82N16O14. Mole weight: 1143.32. | |
| CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 acetate | CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 acetate is the 148-156 amino acid fragment of the BRLF1 protein. BRLF1 is a transcriptional activator that directly binds to the GC-rich motif in the promoter of EBV lytic gene. Alternative Names: L-Arginyl-L-valyl-L-arginyl-L-alanyl-L-tyrosyl-L-threonyl-L-tyrosyl-L-seryl-L-lysine acetate salt; H-Arg-Val-Arg-Ala-Tyr-Thr-Tyr-Ser-Lys-OH.CH3CO2H; L-arginyl-L-valyl-L-arginyl-L-alanyl-L-tyrosyl-L-threonyl-L-tyrosyl-L-seryl-L-lysine acetic acid. Grades: ≥95%. Molecular formula: C53H86N16O16. Mole weight: 1203.35. | |
| CEF2 Influenza Virus PA (46-54) | CEF2 Influenza Virus PA (46-54) is a peptide corresponds to aa 46-54 of the influenza A virus RNA polymerase PA subunit. The PA subunit of the influenza virus polymerase complex is a phosphoprotein that induces proteolytic degradation of coexpressed proteins. Alternative Names: H-Phe-Met-Tyr-Ser-Asp-Phe-His-Phe-Ile-OH; Phe-Met-Tyr-Ser-Asp-Phe-His-Phe-Ile. Molecular formula: C60H75N11O14S. Mole weight: 1206.37. | |
| CEF3 | CEF3 (SIIPSGPLK) corresponds to aa 13-21 of the influenza A virus M1 protein, and was first described in the yeast Saccharomyces cerevisiae and has subsequently been identified in a wide range of fungal species including Candida albicans and Schizosaccharomyces pombe. The matrix (M1) protein of influenza A virus is a multifunctional protein that plays essential structural and functional roles in the virus life cycle. Alternative Names: Influenza Virus M1 (13-21); Ser-Ile-Ile-Pro-Ser-Gly-Pro-Leu-Lys; L-seryl-L-isoleucyl-L-isoleucyl-L-prolyl-L-seryl-glycyl-L-prolyl-L-leucyl-L-lysine. Grades: ≥95%. CAS No. 199727-62-3. Molecular formula: C42H74N10O12. Mole weight: 911.09. | |
| CEF30 Epstein-Barr Virus BRLF1 (134-142) | CEF30 Epstein-Barr Virus BRLF1 (134-142) is a peptide that corresponds to aa 134-142 of the BRLF1 protein from the Epstein-Barr Virus. Alternative Names: H-Ala-Thr-Ile-Gly-Thr-Ala-Met-Tyr-Lys-OH; Ala-Thr-Ile-Gly-Thr-Ala-Met-Tyr-Lys. Molecular formula: C42H70N10O13S. Mole weight: 955.2. | |
| CEF3 acetate | CEF3 acetate corresponds to aa 13-21 of the influenza A virus M1 protein, and was first described in the yeast Saccharomyces cerevisiae and has subsequently been identified in a wide range of fungal species including Candida albicans and Schizosaccharomyces pombe. The matrix (M1) protein of influenza A virus is a multifunctional protein that plays essential structural and functional roles in the virus life cycle. Alternative Names: H-Ser-Ile-Ile-Pro-Ser-Gly-Pro-Leu-Lys-OH.CH3CO2H; L-seryl-L-isoleucyl-L-isoleucyl-L-prolyl-L-seryl-glycyl-L-prolyl-L-leucyl-L-lysine acetic acid. Grades: ≥95%. Molecular formula: C44H78N10O14. Mole weight: 971.16. | |
| CEF4 | CEF4 is a peptide that corresponds to aa 342-351 of the influenza A virus nucleocapsid protein. CEF peptides are v-Src-induced cytokines from chicken embryo fibroblasts. Alternative Names: Influenza Virus NP (342-351); L-arginyl-L-valyl-L-leucyl-L-seryl-L-phenylalanyl-L-isoleucyl-L-lysyl-glycyl-L-threonyl-L-lysine; Arg-Val-Leu-Ser-Phe-Ile-Lys-Gly-Thr-Lys. Grades: ≥95%. CAS No. 199727-68-9. Molecular formula: C53H93N15O13. Mole weight: 1148.39. | |
| CEF4 acetate | CEF4 acetate is a polypeptide that corresponds to amino acid sequence 342-351 of the influenza A virus nucleocapsid protein. CEF peptides are v-Src-induced cytokines from chicken embryo fibroblasts. Alternative Names: H-Arg-Val-Leu-Ser-Phe-Ile-Lys-Gly-Thr-Lys-OH.CH3CO2H; L-arginyl-L-valyl-L-leucyl-L-seryl-L-phenylalanyl-L-isoleucyl-L-lysyl-glycyl-L-threonyl-L-lysine acetic acid; L-Arginyl-L-valyl-L-leucyl-L-seryl-L-phenylalanyl-L-isoleucyl-L-lysylglycyl-L-threonyl-L-lysine acetate salt. Grades: ≥95%. CAS No. 2803406-00-8. Molecular formula: C53H93N15O13.C2H4O2. Mole weight: 1208.45. | |
| CEF6 | CEF6, one of the the CEF control peptides, is a 9-aa-long peptide corresponding to aa 418-426 of the influenza A virus (H1N1) nucleocapsid protein. Alternative Names: CEF6;913545-15-0;CID 146160158;H-DL-Leu-DL-Phe-DL-Phe-DL-Asp-DL-Lys-DL-xiThr-DL-xiThr-DL-Val-DL-Met-OH;4-[[6-amino-1-[[1-[[1-[[1-[(1-carboxy-3-methylsulfanylpropyl)amino]-3-methyl-1-oxobutan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1-oxohexan-2-yl]amino]-3-[[2-[[2-[(2-amino-4-methylpentanoyl)amino]-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-oxobutanoic acid;DA-72061. Grades: ≥95%. CAS No. 913545-15-0. Molecular formula: C31H32O8. Mole weight: 532.6. | |
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