Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| TC 1 | TC 1. Group: Biochemicals. Grades: Purified. CAS No. 362512-81-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| TC 14012 | TC 14012. Group: Biochemicals. Grades: Purified. CAS No. 368874-34-4. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TC 1698 dihydrochloride | TC 1698 dihydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 787587-06-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| 4,5,6,7-Tetrachloro-1H-indene-1,3(2H)-dione (TCID) | Cell-permeable. A potent and selective inhibitor of ubiquitin C-terminal hydrolase L3 (UCH-L3) (IC50=0.6uM). Inhibits ubiquitin C-terminal hydrolase L1 (UCH-L1) only at higher concentrations (IC50 = 75uM). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 25mg. US Biological Life Sciences. | Worldwide |
| b-Catenin/Tcf Inhibitor II, PKF118-310 (1,6-Dimethylpyrimido[5,6-e][1,2,4]triazine-5,7-dione, Wnt Pathway Inhibitor IV) | A synthetic cell-permeable actinobacteria pyrimidotriazine-dione that selectively disrupts b-catenin-Tcf4 interaction (IC50=0.8uM in cell-free binding assays) and inhibits b-catenin-regulated cellular transcription activity (IC50=0.3uM in HCT116-based reporter assays). PKF118-310 is demonstrated to reverse b-catenin, but not siamois, mRNA-induced ventral body axis formation in Xenopus embryos, while direct tumor site injection (1mg/kg/0.5 wk) in HepG2 xenograph mice is shown to increase the number of apoptotic cells and decrease the expression of b-catenin target genes (cyclin D1, c-Myc, survivin) in the tumor mass, resulting in an effective tumor growth retardation (by ~60% after a 4-wk treatment period) in vivo. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Candesartan Cilexetil (TCV 116, 2-Ethoxy-1-[[2'-(2H-tetrazol-5-yl)[1?,1'-biphenyl]-4-yl]methyl]-1H-benzimidazole-7-carbo?xylic acid 1-[[ (cyclohexyloxy) carbonyl]oxy]ethyl ester) | Prodrug of the angiotensin II receptor 1 (AT1) antagonist candesartan, which exhibits antihypertensive effects in animal models. Group: Biochemicals. Grades: Highly Purified. CAS No. 145040-37-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Mecamylamine Hydrochloride (N, 2, 3, 3-Tetramethylbicyclo[2. 2. 1]he-ptan-2-amine hydrochloride, TC-5214, Inversine, nAChR Antagonist, Mecamylamine Hydrochloride) | A potent, nonselective, and noncompetitive antagonist of nAChRs (IC50 = 640nM, 2.5uM, 3.6uM and 6.9uM for alpha3beta4, alpha4beta2, alpha3beta2 and alpha7 subtype nAChRs, respectively). Biologically viable admitted orally or systematically. Widely used in investigating the roles of central nAChRs in the brain functions (learning and memory, decision making, cognition) and disorders (addiction, Autisms, Tourette's syndrome, Schizophrenia and various cognitive and mood disorders). Group: Biochemicals. Grades: Highly Purified. CAS No. 826-39-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Monoclonal Anti-TCF-1 (T-Cell Factor-1) antibody produced in mouse | ~1 mg/mL, clone 7H3, purified immunoglobulin, buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. |  |
| O-((1H)-6-Chlorobenzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TCTU) | 100g Pack Size. Group: Biochemicals, Building Blocks, Diagnostic Raw Materials, Peptide Reagents. Formula: C11H15BClF4N5O. CAS No. 330641-16-2. Prepack ID 20715486-100g. Molecular Weight 355.53. See USA prepack pricing. |  |
| O-((1H)-6-Chlorobenzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TCTU) | 25g Pack Size. Group: Biochemicals, Building Blocks, Diagnostic Raw Materials, Peptide Reagents. Formula: C11H15BClF4N5O. CAS No. 330641-16-2. Prepack ID 20715486-25g. Molecular Weight 355.53. See USA prepack pricing. | |
| TC11 | TC11 is a MCL1 degrader and Caspase-9 and CDK1 activator. TC11 functions as a phenylacetylamide derivative and is structurally related to immunomodulatory active molecules. TC11 induces degradation of MCL1 leading to apoptotic death [1] [2] during prolonged mitotic arrest. Uses: Scientific research. Group: Signaling pathways. CAS No. 100823-03-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129478. |  |
| TC13172 | TC13172 is a mixed lineage kinase domain-like protein (MLKL) inhibitor with an EC50 value of 2 nM for HT-29 cells[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2093393-05-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-101524. | |
| TC14012 | TC 14012 is an antagonist of CXCR4. Synonyms: TC 14012; 368874-34-4; TC 14012 (trifluoroacetate salt); TC14012; H-Arg-Arg-2Nal-Cys(1)-Tyr-Cit-Lys-D-Cit-Pro-Tyr-Arg-Cit-Cys(1)-Arg-NH2; DA-67984; G14057; H-Arg-Arg-Nal-Cys-Tyr-Cit-Lys-DCit-Pro-Tyr-Arg-Cit-Cys-Arg-NH2. Grade: >95%. CAS No. 368874-34-4. Molecular formula: C18H28O5. Mole weight: 324.4. |  |
| TC-A 2317 hydrochloride | TC-A 2317 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 1245907-03-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC AQP1 1 | TC AQP1 1. Group: Biochemicals. Grades: Purified. CAS No. 37710-81-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-AQP1-1 | TC-AQP1-1 is an aquaporin 1 (AQP1) channel blocker. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TC-AQP1-1. Product Category: Others. Appearance: Solid powder. CAS No. 37710-81-9. Molecular formula: C12H10O4. Mole weight: 218.21. Purity: >98%. IUPACName: 3,3'-(1,3-Phenylene)bis(2-propenoic acid). Canonical SMILES: O=C(O)/C=C/C1=CC=CC(/C=C/C(O)=O)=C1. Product ID: ACM37710819. Alfa Chemistry ISO 9001:2015 Certified. |  |
| TC ASK 10 | TC ASK 10. Group: Biochemicals. Grades: Purified. CAS No. 1005775-56-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-C 14G | TC-C 14G. Group: Biochemicals. Grades: Purified. CAS No. 656804-72-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-E 5001 | TC-E 5001. Group: Biochemicals. Grades: Purified. CAS No. 865565-29-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCEP-d12 Hydrochloride | Biochemical tool for selective reduction of disulfide bridges at low pH; reductant for redox assay. Group: Biochemicals. Alternative Names: 3, 3', 3''-Phosphinidynetri spropanoic Acid-d12; Tris(2-carboxyethyl)phosphine-d12 Hydrochloride; Tris (carboxyethyl) phosphine-d12 Hydrochloride. Grades: Highly Purified. CAS No. 1189959-10-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TC-G 1000 | TC-G 1000. Group: Biochemicals. Grades: Purified. CAS No. 245744-18-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1001 | TC-G 1001. Group: Biochemicals. Grades: Purified. CAS No. 494191-73-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1003 | TC-G 1003. Group: Biochemicals. Grades: Purified. CAS No. 1021912-42-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-G 1004 | TC-G 1004. Group: Biochemicals. Grades: Purified. CAS No. 1061747-72-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1006 | TC-G 1006. Group: Biochemicals. Grades: Purified. CAS No. 1324003-64-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G 1008 | TC-G 1008. Group: Biochemicals. Grades: Purified. CAS No. 1621175-65-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-G-1008 | TC-G-1008 (GPR39-C3) is a potent and orally available GPR39 agonist with EC50 values of 0.4 and 0.8 nM for rat and human receptors respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GPR39-C3. CAS No. 1621175-65-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103007. | |
| TC-H 106 | TC-H 106. Group: Biochemicals. Grades: Purified. CAS No. 937039-45-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCH-165 | TCH-165 is a small molecule modulator of proteasome assembly, which increases 20S levels and facilitates 20S-mediated protein degradation[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1446350-60-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-120722. | |
| TC HSD 21 | TC HSD 21. Group: Biochemicals. Grades: Purified. CAS No. 330203-01-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC HSD 21 (5-[ (3-Bromo-4-hydroxyphenyl) methylene]-3- (4-methoxyphenyl) -2-thioxo-4-thiazolidinone) | Potent 17beta-hydroxysteroid dehydrogenase type 3 (17beta-HSD3) inhibitor (IC50 values are 6 and 40nm at human and mouse 17beta-HSD3 respectively). Displays no activity at 17beta-HSD1, 17beta-HSD2, ERalpha, androgen receptors or glucocorticoid receptors. Group: Biochemicals. Grades: Highly Purified. CAS No. 330203-01-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-I 15 | TC-I 15 (TC-I-15) is a type of allosteric collagen-binding integrin ?2?1 inhibitor, and it also inhibits ?1?1 and ?11?1. TC-I 15 inhibits platelet adhesion to collagen and thrombus deposition. TC-I 15 prevents the formation of a pre-metastatic microenvironment by inhibiting the uptake of cancer-associated fibroblast (CAF) extracellular vesicles (EVs) by lung fibroblasts, which reduces the metastasis of salivary gland adenocystic carcinoma (SACC) to the lungs in mouse models, [1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 916734-43-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-107588. | |
| TC-I 2014 | TC-I 2014. Group: Biochemicals. Grades: Purified. CAS No. 1221349-53-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCLP Metals - Ash 1 | certified reference material, pkg of 225 g. Group: Application areas. | |
| TCLP Metals - Loam 1 | certified reference material, pkg of 225 g. Group: Application areas. | |
| TCLP Metals -Loamy Sand 1 | certified reference material, pkg of 225 g. Group: Application areas. | |
| TCLP Metals - Sandy Loam 1 | certified reference material, pkg of 225 g. Group: Application areas. | |
| TCLP Metals - Sandy Loam 12 | certified reference material, pkg of 225 g. Group: Application areas. | |
| TCLP Semi-Volatiles - Sandy Loam 1 | certified reference material, pkg of 225 g. Group: Application areas. | |
| TCMDC-135051 | TCMDC-135051 is a highly selective and potent protein kinase Pf CLK3 inhibitor with low off-target toxicity. TCMDC-135051 prevents trophozoite-to-schizont transition, disrupts transcription and reduces transmission to the mosquito vector. TCMDC-135051 has antiparasiticidal activity (EC 50 =320 nM) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2413716-15-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-126323. | |
| TCMDC-135051 hydrochloride | TCMDC-135051 hydrochloride is a highly selective and potent protein kinase Pf CLK3 inhibitor with low off-target toxicity. TCMDC-135051 hydrochloride prevents trophozoite-to-schizont transition, disrupts transcription and reduces transmission to the mosquito vector. TCMDC-135051 hydrochloride has antiparasiticidal activity (EC 50 =320 nM) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2705545-47-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-126323B. | |
| TC Mps1 12 | TC Mps1 12. Group: Biochemicals. Grades: Purified. CAS No. 1206170-62-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-N 1752 | TC-N 1752. Group: Biochemicals. Grades: Purified. CAS No. 1211866-85-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-N 1752 | TC-N 1752 is a potent and orally active inhibitor of Nav1.7, with IC50s of 0.17 ?M, 0.3 ?M, 0.4 ?M, 1.1 ?M and 2.2 ?M at hNav1.7, hNav1.3, hNav1.4, hNaV1.5 and rNav1.8, respectively. TC-N 1752 also inhibits tetrodotoxin-sensitive sodium channels. TC-N 1752 shows analgesic efficacy in the Formalin model of pain[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1211866-85-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107405. | |
| TCN 201 | TCN 201. Group: Biochemicals. Grades: Purified. CAS No. 852918-02-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCN 213 | TCN 213. Group: Biochemicals. Alternative Names: N-(Cyclohexylmethyl)-2-[[5-[(phenylmethyl)amino]-1,3,4-thiadiazol-2-yl]thio]-acetamide. Grades: Highly Purified. CAS No. 556803-08-8. Pack Sizes: 10mg. Molecular Formula: C18H24N4OS2, Molecular Weight: 376.54. US Biological Life Sciences. | Worldwide |
| TC NTR1 17 | TC NTR1 17. Group: Biochemicals. Grades: Purified. CAS No. 1146757-96-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCNT Type 1- Carbon Nanotubes Thin Walled | TCNT Type 1- Carbon Nanotubes Thin Walled. Group: Nanotubes. CAS No. 308068-56-6. |  |
| TC-O 9311 | TC-O 9311. Group: Biochemicals. Grades: Purified. CAS No. 444932-31-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 1102 | TCS 1102 is a potent, dual orexin receptor antagonist, with Ki values of 0.2 nM and 3 nM for OX2 and OX1 receptors, respectively. TCS 1102 demonstrates excellent blood-brain barrier penetrability and moderate bioavailability in rats[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 916141-36-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-10900. | |
| TCS 1105 | TCS 1105. Group: Biochemicals. Grades: Purified. CAS No. 185391-33-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 1205 | TCS 1205. Group: Biochemicals. Grades: Purified. CAS No. 355022-97-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 183 | TCS 183. Group: Biochemicals. Grades: Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 184 | TCS 184. Group: Biochemicals. Grades: Purified. CAS No. 1315378-71-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 21311 | TCS 21311. Group: Biochemicals. Grades: Purified. CAS No. 1260181-14-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 21311 | TCS 21311 (NIBR3049) is a potent, highly selective JAK3 inhibitor with an IC50 of 8 nM, it displays >100-fold selectivity over JAK1, JAK2 and TYK2. TCS 21311 (NIBR3049) inhibits PKC?, PKC?, and GSK3? with IC50s of 13, 68, and 3 nM, respectively[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NIBR3049. CAS No. 1260181-14-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-108264. | |
| TCS-21311 | A potent JAK3 inhibitor; selective for JAK3 over JAK1, JAK2 and TYK2. It also inhibits GSK-3 β, PKCα and PKC?. Group: Biochemicals. Alternative Names: 3-[5-[4- (2-Hydroxy-2-methyl-1-oxopropyl) -1-piperazinyl]-2- (trifluoromethyl) phenyl]-4- (1H-indol-3-yl) -1H-pyrrole-2, 5-dione; TCS 21311. Grades: Highly Purified. CAS No. 1260181-14-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TCS 2210 | TCS 2210. Group: Biochemicals. Grades: Purified. CAS No. 1201916-31-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS-2210 | TCS 2210 is a small molecule inducer of neuronal differentiation. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TCS-2210; TCS 2210; TCS2210. Product Category: Others. Appearance: To be determined. CAS No. 1201916-31-5. Molecular formula: C18H17N3O3. Mole weight: 323.35. Purity: >98%. IUPACName: 1,2-dihydro-N-hydroxy-2-oxo-3-(3-phenylpropyl)-6-quinoxalinecarboxamide. Canonical SMILES: O=C(C1=CC2=C(NC(C(CCCC3=CC=CC=C3)=N2)=O)C=C1)NO. Product ID: ACM1201916315. Alfa Chemistry ISO 9001:2015 Certified. | |
| TCS 2312 | TCS 2312. Group: Biochemicals. Grades: Purified. CAS No. 838823-31-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 2314 | TCS 2314. Group: Biochemicals. Grades: Purified. CAS No. 317353-73-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS 2510 | TCS 2510. Group: Biochemicals. Grades: Purified. CAS No. 346673-06-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| TCS 401 | TCS 401. Group: Biochemicals. Grades: Purified. CAS No. 243966-09-8. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TCS 5861528 | TCS 5861528. Group: Biochemicals. Grades: Purified. CAS No. 332117-28-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TC-S 7010 | TC-S 7010. Group: Biochemicals. Grades: Purified. CAS No. 1158838-45-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS ERK 11e | Potent and selective extracellular signal-related kinase 2 (ERK2) inhibitor (Ki values are <2, 395, 540 and 852 nM for ERK2, GSK-3, Aurora Kinase A and Cdk2 respectively). Potently blocks proliferation of HT29 cells (IC50 = 48 nM). Orally bioavailable. Group: Biochemicals. Grades: Highly Purified. CAS No. 896720-20-0. Pack Sizes: 10mg. Molecular Formula: C24H20Cl2FN5O2. US Biological Life Sciences. | Worldwide |
| TCS ERK 11e (Potent and Selective ERK2 Inhibitor, 4-[2-[(2-Chloro-4-fluorophenyl)amino]-5-methyl-4-pyrimidinyl]-N-[(1S)-1-(3-chlorophenyl)-2-hydroxyethyl]-1H-pyrrole-2-carboxamide) | Potent and selective extracellular signal-related kinase 2 (ERK2) inhibitor (Ki values are <2, 395, 540 and 852nm for ERK2, GSK-3, Aurora Kinase A and Cdk2 respectively). Potently blocks proliferation of HT29 cells (IC50 = 48nm). Orally bioavailable. Group: Biochemicals. Grades: Highly Purified. CAS No. 896720-20-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| TC-SP 14 | TC-SP 14. Group: Biochemicals. Grades: Purified. CAS No. 1257093-40-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS PIM-1 1 | TCS PIM-1 1. Group: Biochemicals. Grades: Purified. CAS No. 491871-58-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| TCS PIM-1 1 | TCS PIM-1 1 is an ATP-competitive Pim-1 kinase inhibitor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TCS PIM-1 1; SC204330; SC-204330; SC 204330. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 491871-58-0. Molecular formula: C18H11BrN2O2. Mole weight: 367.2. Purity: >98%. IUPACName: 3-Cyano-4-phenyl-6-(3-bromo-6-hydroxy)phenyl-2(1H)-pyridone. Canonical SMILES: O=C1C(C#N)=C(C2=CC=CC=C2)C=C(C3=C(O)C=CC(Br)=C3)N1. Product ID: ACM491871580. Alfa Chemistry ISO 9001:2015 Certified. Categories: 6-(5-bromo-2-hydroxyphenyl)-2-oxo-4-phenyl-1,2-dihydropyridine-3-carbonitrile. | |
Our database is helping our users find suppliers everyday.
