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| Product | Description | |
|---|---|---|
| Protein SSX4 (151-170) | Protein SSX4 (151-170) is a truncated fragment of Protein SSX4. Protein SSX4 may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. Alternative Names: Cancer / testis antigen 5.4 (151-170). |  |
| Protein SSX4 (161-180) | Protein SSX4 (161-180) is a truncated fragment of Protein SSX4. Protein SSX4 may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. Alternative Names: Cancer / testis antigen 5.4 (161-180). | |
| Protein SSX4 (31-50) | Protein SSX4 (31-50) is a truncated fragment of Protein SSX4. Protein SSX4 may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. Alternative Names: Cancer / testis antigen 5.4 (31-50). | |
| Protein SSX4 (41-60) | Protein SSX4 (41-60) is a truncated fragment of Protein SSX4. Protein SSX4 may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. Alternative Names: Cancer / testis antigen 5.4 (41-60). | |
| Protein SSX4 (51-70) | Protein SSX4 (51-70) is a truncated fragment of Protein SSX4. Protein SSX4 may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. Alternative Names: Cancer / testis antigen 5.4 (51-70). | |
| Protein SSX4 (61-80) | Protein SSX4 (61-80) is a truncated fragment of Protein SSX4. Protein SSX4 may function as transcriptional repressors. They are also capable of eliciting spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. Alternative Names: Cancer / testis antigen 5.4 (61-80). | |
| Protein standard | Protein standard. Uses: For analytical and research use. CAS No. 9048-46-8. Catalog: AP9048468-B. |  |
| protein-synthesizing GTPase | This enzyme comprises a family of proteins involved in prokaryotic as well as eukaryotic protein synthesis. In the initiation factor complex, it is IF-2b (98 kDa) that binds GTP and subsequently hydrolyses it in prokaryotes. In eukaryotes, it is eIF-2 (150 kDa) that binds GTP. In the elongation phase, the GTP-hydrolysing proteins are the EF-Tu polypeptide of the prokaryotic transfer factor (43 kDa), the eukaryotic elongation factor EF-1α (53 kDa), the prokaryotic EF-G (77 kDa), the eukaryotic EF-2 (70-110 kDa) and the signal recognition particle that play a role in endoplasmic reticulum protein synthesis (325 kDa). EF-Tu and EF-1α catalyse binding of aminoacyl-tRNA to the ribosomal A-site, while EF-G and EF-2 catalyse the translocation of peptidyl-tRNA from the A-site to the P-site. GTPase activity is also involved in polypeptide release from the ribosome with the aid of the pRFs and eRFs. Group: Enzymes. Synonyms: elongation factor (EF); initiation factor (IF); peptide-release or termination factor. Enzyme Commission Number: EC 3.6.5.3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4714; protein-synthesizing GTPase; EC 3.6.5.3; elongation factor (EF); initiation factor (IF); peptide-release or termination factor. Cat No: EXWM-4714. |  |
| Protein timeless homolog (848-856) | Protein timeless homolog (848-856) is amino acids 848 to 856 fragment of Protein timeless homolog. It plays an important role in the control of DNA replication, maintenance of replication fork stability, maintenance of genome stability throughout normal DNA replication, DNA repair and in the regulation of the circadian clock. This peptide can be used in Ovarian carcinoma research. | |
| protein-tyrosine-phosphatase | Dephosphorylates O-phosphotyrosine groups in phosphoproteins, such as the products of EC 2.7.10.2, non-specific protein-tyrosine kinase. Group: Enzymes. Synonyms: phosphotyrosine phosphatase; phosphoprotein phosphatase (phosphotyrosine); phosphotyrosine histone phosphatase; protein phosphotyrosine phosphatase; tyrosylprotein phosphatase; phosphotyrosine protein phosphatase; phosphotyrosylprotein phosphatase; tyrosine O-phosphate phosphatase; PPT-phosphatase; PTPase; [phosphotyrosine]protein phosphatase; PTP-phosphatase. Enzyme Commission Number: EC 3.1.3.48. CAS No. 79747-53-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3652; protein-tyrosine-phosphatase; EC 3.1.3.48; 79747-53-8; phosphotyrosine phosphatase; phosphoprotein phosphatase (phosphotyrosine); phosphotyrosine histone phosphatase; protein phosphotyrosine phosphatase; tyrosylprotein phosphatase; phosphotyrosine protein phosphatase; phosphotyrosylprotein phosphatase; tyrosine O-phosphate phosphatase; PPT-phosphatase; PTPase; [phosphotyrosine]protein phosphatase; PTP-phosphatase. Cat No: EXWM-3652. | |
| Protein Tyrosine Phosphatase Substrate Monophosphate | Protein Tyrosine Phosphatase Substrate Monophosphate. Uses: For analytical and research use. CAS No. 117872-62-5. Mole weight: 1702.71. Catalog: AP117872625. | |
| protein-tyrosine sulfotransferase | The tyrosine residues of some specific proteins of rat pheochromocytoma cells act as acceptors. Group: Enzymes. Synonyms: tyrosylprotein sulfotransferase. Enzyme Commission Number: EC 2.8.2.20. CAS No. 87588-33-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3379; protein-tyrosine sulfotransferase; EC 2.8.2.20; 87588-33-8; tyrosylprotein sulfotransferase. Cat No: EXWM-3379. | |
| protein xylosyltransferase | Involved in the biosynthesis of the linkage region of glycosaminoglycan chains as part of proteoglycan biosynthesis (chondroitin, dermatan and heparan sulfates). Group: Enzymes. Synonyms: UDP-D-xylose:core protein β-D-xylosyltransferase; UDP-D-xylose:core protein xylosyltransferase; UDP-D-xylose:proteoglycan core protein β-D-xylosyltransferase; UDP-xylose-core protein β-D-xylosyltransferase; uridine diphosphoxylose-core protein β-xylosyltransferase; uridine diphosphoxylose-protein xylosyltransferase. Enzyme Commission Number: EC 2.4.2.26. CAS No. 55576-38-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2653; protein xylosyltransferase; EC 2.4.2.26; 55576-38-0; UDP-D-xylose:core protein β-D-xylosyltransferase; UDP-D-xylose:core protein xylosyltransferase; UDP-D-xylose:proteoglycan core protein β-D-xylosyltransferase; UDP-xylose-core protein β-D-xylosyltransferase; uridine diphosphoxylose-core protein β-xylosyltransferase; uridine diphosphoxylose-protein xylosyltransferase. Cat No: EXWM-2653. | |
| Prothioconazole | 1g Pack Size. Group: Analytical Reagents, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C14H15Cl2N3OS. CAS No. 178928-70-6. Prepack ID 90023720-1g. Molecular Weight 344.2594. See USA prepack pricing. |  |
| Prothioconazole | Prothioconazole is an antifungal agent that can be used as agricultural fungicide and herbicide. Alternative Names: 3H-1,2,4-Triazole-3-thione, 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-; 2-[2-(1-Chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-3H-1,2,4-triazole-3-thione; Acceleron DX 342; JAU 6476; Joao; Proline (fungicide); Proline 275; Proline 480SC; Redigo; Rudis. Grades: >95%. CAS No. 178928-70-6. Molecular formula: C14H15Cl2N3OS. Mole weight: 344.26. | |
| Prothionamide | Prothionamide. Group: Biochemicals. Alternative Names: 2-propyl -4-pyridinecarbothioamide ; 2-propyl thioisonicotinamide; 2-propyl isonicotinylthioamide. Grades: Highly Purified. CAS No. 14222-60-7. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C9H12N2S. US Biological Life Sciences. |  Worldwide |
| Prothipendyl hydrochloride | Prothipendyl hydrochloride. Group: Biochemicals. Alternative Names: N,N-Dimethyl-10H-pyrido[3,2-b][1,4]benzothiazine-10-propanamine hydrochloride; AY 56031; Azacon. Grades: Highly Purified. CAS No. 1225-65-6. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H20ClN3S. US Biological Life Sciences. | Worldwide |
| Prothipendyl hydrochloride | Prothipendyl hydrochloride is a tricyclic azaphenothiazine neuroleptic agent. Prothipendyl hydrochloride is a substrate of the CYP isozymes CYP1A2, CYP2D6, CYP2C19 and CYP3A4. Prothipendyl hydrochloride has sedating and psychomotorically damping effects. Prothipendyl hydrochloride can be used for psychomotoric agitation, sleep disorder and anxiety research [1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1225-65-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg. Product ID: HY-116780A. |  |
| Prothipendyl sulphoxide | Prothipendyl sulphoxide. Alternative Names: N,N-Dimethyl-10H-pyrido[3,2-b][1,4]benzothiazine-10-propanamine 5-Oxide. CAS No. 10071-01-9. Purity: 96%. Product ID: ACM10071019. Molecular formula: C16H19N3OS. Mole weight: 301.41. IUPAC Name: N,N-dimethyl-3-(5-oxopyrido[3,2-b][1,4]benzothiazin-10-yl)propan-1-amine. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Prothracarcin | Prothracarcin is an antitumor antibiotic produced by Str. umbrosus subsp. raffinophilus DO-62. It is active against Gram-positive and Gram-negative bacteria and experimental murine tumor sarcoma 180 and leukemia P388. Alternative Names: Antibiotic DC 62. Grades: >98%. CAS No. 81542-99-6. Molecular formula: C14H14N2O. Mole weight: 226.27. | |
| Protionamide | An anti-tuberculosis agent. It has also been used to treat Leprosy. Antibacterial (tuberculostatic). Group: Biochemicals. Alternative Names: 2-propyl -4-pyridinecarbothioamide ; 2-propyl thioisonicotinamide; 2-propyl isonicotinylthioamide; 9778 R. P.; Ektebin; Prothionamide; Protion; Protionamid; Protionizina; RP 9778; TH 1321; Tebeform; Trevintix; Tuberex. Grades: Highly Purified. CAS No. 14222-60-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Protionamide | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Pyridines, Pyrimidines. Formula: C9H12N2S. CAS No. 14222-60-7. Prepack ID 89981934-5g. Molecular Weight 180.27. See USA prepack pricing. | |
| Protirelin | Protirelin is a highly conserved neuropeptide that exerts the hormonal control of thyroid-stimulating hormone (TSH) levels as well as neuromodulatory functions. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Thyrotropin-releasing-hormone; TRH. CAS No. 24305-27-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P0002. | |
| Protirelin acetate | Protirelin Acetate is a highly conserved neuropeptide that exerts the hormonal control of thyroid-stimulating hormone (TSH) levels as well as neuromodulatory functions. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Thyrotropin-releasing-hormone acetate; TRH acetate. CAS No. 120876-23-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P0002A. | |
| Protirelin Acetate | Protirelin Acetate is a highly conserved neuropeptide that plays a hormonal role in controlling thyroid-stimulating hormone (TSH) levels and neuromodulatory functions. Alternative Names: TRF Acetate; TRH Acetate; TSH-RF Acetate; pGlu-HP-NH2; L-pyroglutamyl-L-histidyl-L-prolinamide acetic acid; 5-Oxo-L-prolyl-L-histidyl-L-prolinamide acetate (2:3). Grades: ≥95%. CAS No. 120876-23-5. Molecular formula: C16H22N6O4.3/2C2H4O2. Mole weight: 452.46. | |
| protoaphin-aglucone dehydratase (cyclizing) | The product is converted non-enzymically to erythroaphin, an aphid pigment. Group: Enzymes. Synonyms: protoaphin dehydratase; protoaphin dehydratase (cyclizing); protoaphin-aglucone hydro-lyase (cyclizing). Enzyme Commission Number: EC 4.2.1.73. CAS No. 64177-87-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5057; protoaphin-aglucone dehydratase (cyclizing); EC 4.2.1.73; 64177-87-3; protoaphin dehydratase; protoaphin dehydratase (cyclizing); protoaphin-aglucone hydro-lyase (cyclizing). Cat No: EXWM-5057. | |
| protoasukamycin 4-monooxygenase | The enzyme, characterized from the bacterium Streptomyces nodosus subsp. asukaensis, is involved in the biosynthesis of the antibiotic asukamycin. Requires a flavin cofactor, with no preference among FMN, FAD or riboflavin. When flavin concentration is low, activity is enhanced by the presence of the NADH-dependent flavin-reductase AsuE2. Group: Enzymes. Enzyme Commission Number: EC 1.14.13.215. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0817; protoasukamycin 4-monooxygenase; EC 1.14.13.215. Cat No: EXWM-0817. | |
| Protocatechualdehyde | Protocatechualdehyde. Group: Biochemicals. Alternative Names: 3,4-Dihydroxybenzaldehyde; Protocatechuic aldehyde; Rancinamycin IV. Grades: Plant Grade. CAS No. 139-85-5. Pack Sizes: 100mg. Molecular Formula: C7H6O3, Molecular Weight: 138.121. US Biological Life Sciences. | Worldwide |
| Protocatechualdehyde | Protocatechualdehyde. Alternative Names: 1,2-Dihydroxy-4-formylbenzene. CAS No. 139-85-5. Purity: 98%. Product ID: ACM139855. Molecular formula: C7H6O3. Mole weight: 138.12. IUPAC Name: 3,4-Dihydroxybenzaldehyde. Alfa Chemistry - ISO 9001:32057 Certified. | |
| protocatechuate 3,4-dioxygenase | Requires Fe3+. The enzyme, which participates in the degradation of aromatic compounds, catalyses the intradiol addition of both oxygen atoms from molecular oxygen, resulting in ortho-cleavage of the aromatic ring. The type of cleavage leads to mineralization via the intermediate 3-oxoadipate. Group: Enzymes. Synonyms: protocatechuate oxygenase; protocatechuic acid oxidase; protocatechuic 3,4-dioxygenase; protocatechuic 3,4-oxygenase; protocatechuate:oxygen 3,4-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.3. CAS No. 9029-47-4. Protocatechuate 3, 4-dioxygenase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0549; protocatechuate 3,4-dioxygenase; EC 1.13.11.3; 9029-47-4; protocatechuate oxygenase; protocatechuic acid oxidase; protocatechuic 3,4-dioxygenase; protocatechuic 3,4-oxygenase; protocatechuate:oxygen 3,4-oxidoreductase (decyclizing). Cat No: EXWM-0549. | |
| Protocatechuate 3,4-dioxygenase | Protocatechuate 3,4-dioxygenase is a dioxygenase. Protocatechuate 3,4-dioxygenase belongs to the non-heme iron dioxygenase class. Protocatechuate 3,4-dioxygenase catalyzes the cleavage of the aromatic ring of 3,4-dihydroxybenzoate, attaching two atoms of molecular oxygen to the compound to generate β-carboxy-cis,cis-muconate. Protocatechuate 3,4-dioxygenase is a key enzyme in the β-ketoadipic acid pathway. It is found in marine bacteria associated with Roseobacter. Protocatechuate 3,4-dioxygenase can be isolated from Pseudomonas aeruginosa[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9029-47-4. Pack Sizes: 25 U; 50 U; 100 U. Product ID: HY-P2915. | |
| Protocatechuate 3,4-Dioxygenase from Bacteria, Recombinant | In enzymology, a protocatechuate 3,4-dioxygenase (EC 1.13.11.3) is an enzyme that catalyzes the chemical reaction:3,4-dihydroxybenzoate + O2<-> 3-carboxy-cis,cis-muconate. Thus, the two substrates of this enzyme are 3,4-dihydroxybenzoate (protocatechuic acid) and O2, whereas its product is 3-carboxy-cis,cis-muconate. This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). This enzyme participates in benzoate degradation via hydroxylation and 2,4-dichlorobenzoate degradation. It employs one cofactor, iron. Applications: Useful for removal of protocatechuate derived from choline esterase determination. Group: Enzymes. Synonyms: protocatechuate 3,4-dioxygenase; protocatechuate oxygenase; protocatechuic acid oxidase; protocatech. Enzyme Commission Number: EC 1.13.11.3. CAS No. 9029-47-4. Protocatechuate 3, 4-dioxygenase. Mole weight: 28 kD α subuit, 24 kD β subunit?SDS-PAGE?. Activity: > 3 Units / mg. Storage: 1 - 10°C (do not freeze). Form: Solution. Source: E. coli. Species: Bacteria. protocatechuate 3,4-dioxygenase; protocatechuate oxygenase; protocatechuic acid oxidase; protocatechuic 3,4-dioxygenase; protocatechuic 3,4-oxygenase; 9029-47-4; EC 1.13.11.3; PCD. Cat No: NATE-1028. | |
| protocatechuate 4,5-dioxygenase | Requires Fe2+. Group: Enzymes. Synonyms: protocatechuate 4,5-oxygenase; protocatechuic 4,5-dioxygenase; protocatechuic 4,5-oxygenase; protocatechuate:oxygen 4,5-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.8. CAS No. 9029-56-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0600; protocatechuate 4,5-dioxygenase; EC 1.13.11.8; 9029-56-5; protocatechuate 4,5-oxygenase; protocatechuic 4,5-dioxygenase; protocatechuic 4,5-oxygenase; protocatechuate:oxygen 4,5-oxidoreductase (decyclizing). Cat No: EXWM-0600. | |
| protocatechuate decarboxylase | This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in benzoate degradation via hydroxylation. Group: Enzymes. Synonyms: 3,4-dihydrobenzoate decarboxylase; protocatechuate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.63. CAS No. 37290-55-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4810; protocatechuate decarboxylase; EC 4.1.1.63; 37290-55-4; 3,4-dihydrobenzoate decarboxylase; protocatechuate carboxy-lyase. Cat No: EXWM-4810. | |
| Protocatechuic acid | Protocatechuic acid is a phenolic compound which exhibits neuroprotective effect. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 3,4-Dihydroxybenzoic acid. CAS No. 99-50-3. Pack Sizes: 10 mM * 1 mL in DMSO; 200 mg; 1 g. Product ID: HY-N0294. | |
| Protocatechuic Acid | Protocatechuic Acid. Group: Biochemicals. Alternative Names: Carbohydroquinonic acid; Catechol-4-carboxylic acid; Hypogallic acid. Grades: Plant Grade. CAS No. 99-50-3. Pack Sizes: 20mg. Molecular Formula: C7H6O4, Molecular Weight: 154.12. US Biological Life Sciences. | Worldwide |
| Protocetraric acid | Protocetraric acid has strong antioxidant, antibacterial and anticancer effects. Alternative Names: 11H-Dibenzo(b,e)(1,4)dioxepin-7-carboxylic acid, 4-formyl-3,8-dihydroxy-9-(hydroxymethyl)-1,6-dimethyl-11-oxo-; 10-formyl-3,9-dihydroxy-4-(hydroxymethyl)-1,7-dimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylic acid; Protocetrarsaeure. Grades: ≥98%. CAS No. 489-51-0. Molecular formula: C18H14O9. Mole weight: 374.30. | |
| protochlorophyllide reductase | The enzyme catalyses a light-dependent trans-reduction of the D-ring of protochlorophyllide; the product has the (7S,8S)-configuration. Group: Enzymes. Synonyms: NADPH2-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide reductase; protochlorophyllide oxidoreductase (ambiguous); protochlorophyllide photooxidoreductase; light-dependent protochlorophyllide reductase. Enzyme Commission Number: EC 1.3.1.33. CAS No. 68518-04-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1306; protochlorophyllide reductase; EC 1.3.1.33; 68518-04-7; NADPH2-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide oxidoreductase; NADPH-protochlorophyllide reductase; protochlorophyllide oxidoreductase (ambiguous); protochlorophyllide photooxidoreductase; light-dependent protochlorophyllide reductase. Cat No: EXWM-1306. | |
| Protodeltonin | Protodeltonin. Group: Biochemicals. Grades: Plant Grade. CAS No. 94992-08-2. Pack Sizes: 10mg. Molecular Formula: C51H84O23, Molecular Weight: 1065.21. US Biological Life Sciences. | Worldwide |
| protodeoxyviolaceinate monooxygenase | The enzyme, characterized from the bacterium Chromobacterium violaceum, participates in the biosynthesis of the violet pigment violacein. The product, protoviolaceinate, can be acted upon by EC 1.14.13.224, violacein synthase, leading to violacein production. However, it is very labile, and in the presence of oxygen can undergo non-enzymic autooxidation to the shunt product proviolacein. Group: Enzymes. Synonyms: vioD (gene name); protoviolaceinate synthase. Enzyme Commission Number: EC 1.14.13.217. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0819; protodeoxyviolaceinate monooxygenase; EC 1.14.13.217; vioD (gene name); protoviolaceinate synthase. Cat No: EXWM-0819. | |
| Protodioscin | Protodioscin. Group: Biochemicals. Alternative Names: Saponin C. Grades: Plant Grade. CAS No. 55056-80-9. Pack Sizes: 20mg. Molecular Formula: C51H84O22, Molecular Weight: 1049.2. US Biological Life Sciences. | Worldwide |
| Protodioscin | Protodioscin, a major steroidal saponin in Trigonella foenum-graecum Linn., has been shown to exhibit multiple biological actions, such as anti-hyperlipidemia, anti-cancer, sexual effects and cardiovascular properties. Uses: Scientific research. Category: Signaling pathways. CAS No. 55056-80-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0799. | |
| protodioscin 26-O-β-D-glucosidase | The enzyme has been characterized from the plants Cheilocostus speciosus and Solanum torvum. It also hydrolyses the 26-β-D-glucose group from related steroid glucosides such as protogracillin, torvoside A and torvoside H. Group: Enzymes. Synonyms: F26G; torvosidase; CSF26G1; furostanol glycoside 26-O-β-D-glucosidase; furostanol 26-O-β-D-glucoside glucohydrolase. Enzyme Commission Number: EC 3.2.1.186. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3870; protodioscin 26-O-β-D-glucosidase; EC 3.2.1.186; F26G; torvosidase; CSF26G1; furostanol glycoside 26-O-β-D-glucosidase; furostanol 26-O-β-D-glucoside glucohydrolase. Cat No: EXWM-3870. | |
| Protoescigenin | Protoescigenin is the main aglycone of horse chestnut saponin mixture known as escin. Protoescigenin is selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene[1]. Uses: Scientific research. Category: Natural products. CAS No. 20853-07-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N7497. | |
| Protogracillin | Protogracillin is a steroidal furostanol saponin. Protogracillin can be isolated from the rhizomes and tubers of Dioscorea zingiberensis C.H. Wright. Protogracillin is hydrolyzable to Prosapogenin A (HY-N6940). Protogracillin exhibits antithrombotic activity. Protogracillin can be used in research related to cardiovascular diseases[1][2]. Uses: Scientific research. Category: Natural products. CAS No. 54848-30-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-N4271. | |
| Protogracillin | Protogracillin. Group: Biochemicals. Grades: Plant Grade. CAS No. 54848-30-5. Pack Sizes: 10mg. Molecular Formula: C51H84O23, Molecular Weight: 1065.21. US Biological Life Sciences. | Worldwide |
| Protohypericin | Protohypericin is a quinone isolated from Hypericum perforatum showing photocytotoxicity. Alternative Names: 1,3,4,6,8,15-Hexahydroxy-10,13-dimethyl-dibenzo[a,o]perylene-7,16-dione. Grades: 0.98. CAS No. 548-03-8. Molecular formula: C30H18O8. Mole weight: 506.46. | |
| Protohypericin | Protohypericin is a compound that can be extracted from Hypericum perforatum. Protohypericin has low photocytotoxicity but can be efficiently photoconverted into Hypericin (HY-N0453) with high phototoxicity under visible light. Protohypericin can be used in cancer research[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 548-03-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-N4139. | |
| Protokylol hydrochloride | Protokylol hydrochloride (Caytine hydrochloride; JB-251 hydrochloride) is the hydrochloride salt form of Protokylol (HY-114630). Protokylol hydrochloride is an agonist for β2-adrenergic receptor and TRPV1. Protokylol hydrochloride exhibits activity as a bronchodilator[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Caytine hydrochloride; JB-251 hydrochloride. CAS No. 136-69-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-16413. | |
| Protoneogracillin | Protoneogracillin is a furostanol glycoside that has anti-fungal activity against the plant pathogenic fungus P. oryzae (MMDC = 94.0 μM) and cytotoxic activity on K562 cancer cells (IC50 = 6.6 μM). Alternative Names: Protogracillin; (3β,22R,25S)-26-(β-D-Glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl 6-deoxy-α-L-mannopyranosyl-(1->2)-[β-D-glucopyranosyl-(1->3)]-β-D-glucopyranoside; β-D-Glucopyranoside, (3β,22β,25S)-26-(β-D-glucopyranosyloxy)-22-hydroxyfurost-5-en-3-yl O-6-deoxy-α-L-mannopyranosyl-(1->2)-O-[β-D-glucopyranosyl-(1->3)]-. Grades: ≥95%. CAS No. 191334-50-6. Molecular formula: C51H84O23. Mole weight: 1065.20. | |
| proton-translocating NAD(P)+ transhydrogenase | The enzyme is a membrane bound proton-translocating pyridine nucleotide transhydrogenase that couples the reversible reduction of NADP by NADH to an inward proton translocation across the membrane. In the bacterium Escherichia coli the enzyme provides a major source of cytosolic NADPH. Detoxification of reactive oxygen species in mitochondria by glutathione peroxidases depends on NADPH produced by this enzyme. Group: Enzymes. Synonyms: pntA (gene name); pntB (gene name); NNT (gene name). Enzyme Commission Number: EC 7.1.1.1 (Formerly EC 1.6.1.5). Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1578; proton-translocating NAD(P)+ transhydrogenase; EC 1.6.1.5; pntA (gene name); pntB (gene name); NNT (gene name). Cat No: EXWM-1578. | |
| Proto-oncogene PIM1 (191-199) | Proto-oncogene PIM1 (191-199) is a 9-aa peptide. Pim-1's role in oncogenic signalling has led to it becoming a widely studied target in cancer research, with numerous drug candidates under investigation which target it. | |
| protopanaxadiol 6-hydroxylase | A heme-thiolate protein (P-450). Involved in the biosynthetic pathway of ginsenosides. Isolated from the rhizomes of ginseng (Panax ginseng). Group: Enzymes. Synonyms: protopanaxatriol synthase; P6H; CYP716A53v2; protopanaxadiol,NADPH:O2 oxidoreductase (6α-hydroxylating). Enzyme Commission Number: EC 1.14.13.184. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0783; protopanaxadiol 6-hydroxylase; EC 1.14.13.184; protopanaxatriol synthase; P6H; CYP716A53v2; protopanaxadiol,NADPH:O2 oxidoreductase (6α-hydroxylating). Cat No: EXWM-0783. | |
| Protopanaxatriol | Botanical Source: Group: Biochemicals. Alternative Names: (20R)-Protopanaxatriol. Grades: Plant Grade. CAS No. 1453-93-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Protopanaxatriol | 20S-Protopanaxatriol (g-PPT), a dammarane-type tetracyclic terpene sapogenin, may be used to study its binding to and modulation of cell function via glucocortoid (GR) and oestrogen (ER) receptors. Protopanaxatriol can be used in health products. Alternative Names: 20(S)-APPT; g-PPT. Grades: >98%. CAS No. 34080-08-5. Molecular formula: C30H52O4. Mole weight: 476.73. | |
| Protopanaxatriol, 20S- | Protopanaxatriol, 20S-. Group: Biochemicals. CAS No. 34080-08-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Protopine | Protopine is an alkaloid isolated from the tubers of Corydalis yanhusuo W.T.Wang. It shows weak spasmolytic, smooth muscle stimulant activities. Uses: Bactericidal; sedative; antihypertensive. Alternative Names: 7-Methyl-6,8,9,16-tetrahydrodi[1,3]benzodioxolo[4,5-c:5,6-g]azecin-15(7H)-one; Biflorine. Grades: 98%. CAS No. 130-86-9. Molecular formula: C20H19NO5. Mole weight: 353.4. | |
| Protopine | Protopine is a Ca2+ channel blocker and antiplatelet agent. Immunomodulator. Group: Biochemicals. Alternative Names: 4,6,7,14-Tetrahydro-5-methyl-. Grades: Highly Purified. CAS No. 130-86-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Protopine | Protopine (Corydinine), an isoquinoline alkaloid, is a specific reversible and competitive inhibitor of acetylcholinesterase. Protopine exhibits anti-inflammation, anti-microbial, anti-angiogenic and anti-tumour activity[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Corydinine. CAS No. 130-86-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0793. | |
| protopine 6-monooxygenase | A heme-thiolate protein (P-450) involved in benzophenanthridine alkaloid synthesis in higher plants. Group: Enzymes. Synonyms: protopine 6-hydroxylase. Enzyme Commission Number: EC 1.14.13.55. CAS No. 128561-60-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0862; protopine 6-monooxygenase; EC 1.14.13.55; 128561-60-4; protopine 6-hydroxylase. Cat No: EXWM-0862. | |
| Protoporphyrinato zinc | Protoporphyrinato zinc. Alternative Names: PROTOPORPHYRINATO ZINC;dihydrogen [3,8,13,17-tetramethyl-7,12-divinyl-21H,23H-porphine-2,18-dipropionato(4-)-N21,N22,N23,N24]zincate(4-);Zinc protoporphyrin trihydrate;Zinc protoporphyrin trihydrate, 95+%. CAS No. 15442-64-5. Molecular formula: C34H32N4O4Zn. Mole weight: 626g/mol. IUPAC Name: zinc;3-[18-(2-carboxyethyl)-8,13-bis(ethenyl)-3,7,12,17-tetramethylporphyrin-21,23-diid-2-yl]propanoic acid. SMILES: CC1=C(C2=CC3=NC(=CC4=C(C(=C([N-]4)C=C5C(=C(C(=N5)C=C1[N-]2)C)C=C)C)C=C)C(=C3CCC(=O)O)C)CCC(=O)O.[Zn+2]. InChI: InChI=1S/C34H34N4O4.Zn/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-2. |  |
| protoporphyrin ferrochelatase | The enzyme catalyses the terminal step in the heme biosynthesis pathways of eukaryotes and Gram-negative bacteria. Group: Enzymes. Synonyms: ferro-protoporphyrin chelatase; iron chelatase (ambiguous); heme synthetase (ambiguous); heme synthase (ambiguous); protoheme ferro-lyase; ferrochelatase (ambiguous). Enzyme Commission Number: EC 4.99.1.1. CAS No. 9012-93-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5358; protoporphyrin ferrochelatase; EC 4.99.1.1; 9012-93-5; ferro-protoporphyrin chelatase; iron chelatase (ambiguous); heme synthetase (ambiguous); heme synthase (ambiguous); protoheme ferro-lyase; ferrochelatase (ambiguous). Cat No: EXWM-5358. | |
| Protoporphyrin IX | Protoporphyrin IX is an important precursor to biologically essential prosthetic groups such as heme, cytochrome c, and chlorophylls. As a result, a number of organisms are able to synthesize this tetrapyrrole from basic precursors such as glycine and succinyl CoA, or glutamate. Despite the wide range of organisms that synthesize protoporphyrin IX the process is largely conserved from bacteria to mammals with a few distinct exceptions in higher plants.[1][2][3]. Group: Biochemicals. Alternative Names: 3,18-Divinyl-2,7,13,17-tetramethylporphine-8, 12-dipropionic acid. Grades: Reagent Grade. CAS No. 553-12-8. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Protoporphyrin IX | Protoporphyrin IX is a final intermediate in the heme biosynthetic pathway, which acts as a radiation sensitizer enhancing ROS generation even in a hypoxic state and inducing DNA damage. Protoporphyrin IX also acts as a photo sensitizer undergoing photobleaching that occurs through direct degradation by light irradiation. Protoporphyrin IX is formed and accumulated following 5-aminolevulinic acid (5-ALA) (HY-W000450) administration in the tumor cells of rats. Protoporphyrin IX causes selective improvement of basal cell carcinoma when activated red fluorescence of a peak wavelength at 405 nm. Protoporphyrin IX is promising for research of sonodynamic and photodynamic agents for a wide range of cancers, such as bladder cancer and nodular basal cell carcinoma[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PPIX. CAS No. 553-12-8. Pack Sizes: 100 mg; 250 mg. Product ID: HY-B1247. | |
| Protoporphyrin IX | Created by the enzyme protoporphyrinogen oxidase, protoporphyrin IX is an important precursor to biologically essential prosthetic groups. Uses: Metabolism of porphyrin. Alternative Names: Protoporphyrin; 3-[18-(2-carboxyethyl)-8,13-bis(ethenyl)-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoic acid. Grades: ≥95%. CAS No. 553-12-8. Molecular formula: C34H34N4O4. Mole weight: 562.66. | |
| Protoporphyrin IX cobalt chloride | Protoporphyrin IX cobalt chloride. Alternative Names: Protoporphyrin IX cobalt chloride;102601-60-5;Co(iII) protoporphyrin ix chloride. CAS No. 102601-60-5. Product ID: ACM102601605. Molecular formula: C34H32ClCoN4O4. Mole weight: 655.037g/mol. IUPAC Name: 3-[18-(2-carboxyethyl)-7,12-bis(ethenyl)-3,8,13,17-tetramethylporphyrin-21,23-diid-2-yl]propanoic acid;chlorocobalt(2+). Alfa Chemistry - ISO 9001:32057 Certified. | |
| Protoporphyrin IX-d6 | Protoporphyrin IX-d6 is the labeled version of Protoporphyrin IX (CAS: 553-12-8). Protoporphyrin IX (PPIX) is ubiquitously present in all living cells in small amounts as a precursor of heme and PPIX-based strategies have been used for cancer diagnosis and treatment. It can be used in biological study for role of protoporphyrin IX in skin photosensitivity, biliary stones, hepatobiliary damage, liver failure and cancer diagnosis and treatment in human. Group: Biochemicals. Alternative Names: Protoporphyrin IX di-Me Ester-d6; 3,7,12,17-Tetramethyl-8,13-divinyldimethyl Ester 2,18-Porphinedipropionic Acid-d6. Grades: Highly Purified. CAS No. 553-12-8 Unlabeled. Pack Sizes: 500ug, 2.5mg. Molecular Formula: C??H??D?N?O?, Molecular Weight: 596.75. US Biological Life Sciences. | Worldwide |
| Protoporphyrin IX dimethyl ester | Protoporphyrin IX dimethyl ester. Alternative Names: Dimethyl 3,3'-(3,8,13,17-Tetramethyl-7,12-divinylporphyrin-2,18-diyl)dipropionate. CAS No. 5522-66-7. Purity: >95.0%. Product ID: FFC-AR-5522667. Molecular formula: C36H38N4O4. Mole weight: 590.71. IUPAC Name: methyl 3-[8,13-bis(ethenyl)-18-(3-methoxy-3-oxopropyl)-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Protoporphyrin IX (Standard) | Protoporphyrin IX (Standard) is the analytical standard of Protoporphyrin IX. This product is intended for research and analytical applications. Protoporphyrin IX is a final intermediate in the heme biosynthetic pathway, which acts as a radiation sensitizer enhancing ROS generation even in a hypoxic state and inducing DNA damage. Protoporphyrin IX also acts as a photo sensitizer undergoing photobleaching that occurs through direct degradation by light irradiation. Protoporphyrin IX is formed and accumulated following 5-aminolevulinic acid (5-ALA) (HY-W000450) administration in the tumor cells of rats. Protoporphyrin IX causes selective improvement of basal cell carcinoma when activated red fluorescence of a peak wavelength at 405 nm. Protoporphyrin IX is promising for research of sonodynamic and photodynamic agents for a wide range of cancers, such as bladder cancer and nodular basal cell carcinoma[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PPIX (Standard). CAS No. 553-12-8. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1247R. | |
| protoporphyrinogen IX dehydrogenase (menaquinone) | This enzyme enables Escherichia coli to synthesize heme in both aerobic and anaerobic environments. Group: Enzymes. Synonyms: HemG. Enzyme Commission Number: EC 1.3.5.3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1387; protoporphyrinogen IX dehydrogenase (menaquinone); EC 1.3.5.3; HemG. Cat No: EXWM-1387. | |
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