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| Product | Description | |
|---|---|---|
| CD274 human | recombinant, expressed in E. coli, 0.5 mg protein/mL. Group: Fluorescence/luminescence spectroscopy. |  |
| CD276 human | recombinant, expressed in E. coli, 0.5 mg protein/mL. Group: Fluorescence/luminescence spectroscopy. | |
| CD279 (human): FC (human) | recombinant, expressed in CHO cells, ?98% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Cd2+-exporting ATPase | A P-type ATPase that undergoes covalent phosphorylation during the transport cycle. This enzyme occurs in protozoa, fungi and plants. Group: Enzymes. Enzyme Commission Number: EC 3.6.3.3. 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-4667; Cd2+-exporting ATPase; EC 3.6.3.3. Cat No: EXWM-4667. |  |
| CD2 human | recombinant, expressed in E. coli, 0.5 mg protein/mL. Group: Fluorescence/luminescence spectroscopy. | |
| CD-3 | CD-3 (Part#: 1090) |  |
| CD300A human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD300C human | recombinant, expressed in E. coli, ?85% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD304/NRP1/Neurophilin-1 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD306/LAIR2 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD30/TNFRSF8 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD31 | CD31 (PECAM-1) is platelet endothelial cell adhesion molecule-1, serves as the endothelial cell-specific receptor of clostridium perfringens b-Toxin ( CPB ). CD31 is also an ER-MP12 antigen , acts as a linker between mechanical stress, metabolism and inflammation. CD31 peptide is able to sustain phosphorylation of the CD31 ITIM 686 and of SHP2 and to inhibit TCR -induced T-cell activation [1] - [5]. Uses: Scientific research. Group: Peptides. Alternative Names: PECAM-1. CAS No. 161374-99-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3444. |  |
| CD319/SLAMF7/CRACC human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD3254 | CD3254 a potent and selective retinoid-X-receptor (RXR) agonist[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 196961-43-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-107399. | |
| CD 3254 | CD 3254 is a selective RXRα agonist with no activity at RARα, RARβ or RARγ receptors. Synonyms: CD3254; CD 3254; CD-3254. 3-[4-Hydroxy-3-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)phenyl]-2-propenoic acid. Grade: ≥97% by HPLC. CAS No. 196961-43-0. Molecular formula: C24H28O3. Mole weight: 364.48. |  |
| CD 3254 | CD 3254. Group: Biochemicals. Grades: Purified. CAS No. 196961-43-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| CD34+ Cells Targeted SM102 LNP-EGFP mRNA (m1Ψ) | This product is a LNP prepared from SM102 as the ionizable lipid and modified with CD34 antibody. It's specifically designed for targeted delivery of EGFP mRNA to CD34 positive cells. EGFP mRNA, a common fluorescence reporter, translates into enhanced green fluorescent protein, which exhibits an excitation wavelength of 488 nm and emission at 507 nm. The loaded EGFP mRNA is modified with N1-methyl-pseudouridine to enhance expression and reduce immunogenicity. It is only for research purposes. Group: Lipid nanoparticle. |  |
| CD36 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD38 inhibitor 1 | CD38 inhibitor 1 (compound 78c) is a potent CD38 inhibitor with IC50s of 7.3 nM and 1.9 nM for hCD38 and mouse CD38[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1700637-55-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-123999. | |
| CD38 inhibitor 1 | CD38 inhibitor 1 is a potent CD38 inhibitor. Synonyms: CD38-IN-78c; MDK-7553. CAS No. 1700637-55-3. Molecular formula: C22H27N3O3S. Mole weight: 413.53. | |
| CD3E human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD3G human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD-4 | CD-4 (Part#: 1095) | |
| CD40 human | recombinant, expressed in E. coli, 0.5 mg protein/mL. Group: Fluorescence/luminescence spectroscopy. | |
| CD40Ligand/TRAP from mouse | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| CD40L, Soluble human | recombinant, expressed in CHO cells, >95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD40L, Soluble mouse | recombinant, expressed in CHO cells, >95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD40-TRAF6 inhibitor | A CD40-TRAF6 interaction inhibitor. Synonyms: 3-[(2,5-Dimethylphenyl)amino]-1-phenyl-2-propen-1-one. CAS No. 433249-94-6. Molecular formula: C17H17NO. Mole weight: 251.32. | |
| CD437 | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| CD437 | CD437 is a selective Retinoic Acid Receptor γ (RARγ) agonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AHPN. CAS No. 125316-60-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100532. | |
| CD 437 | CD 437. Group: Biochemicals. Grades: Purified. CAS No. 125316-60-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| CD 437 (AHPN, CD437, O-Desmethyl Adapalene, 6-(4-Hydroxy-3-tricyclo[3.3.1.13, 7]dec-1-ylphenyl)-2-naphthalenecarboxylic Acid) | CD 437 (AHPN, CD437, O-Desmethyl Adapalene, 6-(4-Hydroxy-3-tricyclo[3.3.1.13, 7]dec-1-ylphenyl)-2-naphthalenecarboxylic Acid). Group: Biochemicals. Alternative Names: 6- [3- (1-adamantyl) -4-hydroxyphenyl] naphthalene-2-carboxylic acid. Grades: Highly Purified. CAS No. 125316-60-1. Pack Sizes: 10mg, 50mg. Molecular Formula: C27 H26 O3, Molecular Weight: 398.5. US Biological Life Sciences. | Worldwide |
| CD45 Active human | recombinant, expressed in baculovirus infected insect cells, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD46 human | recombinant, expressed in E. coli, ?85% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD47 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD48/BCM1/SLAMF2 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD532 | CD532 is a potent Aurora A kinase inhibitor with an IC 50 of 45 nM. CD532 has the dual effect of blocking Aurora A kinase activity and driving degradation of MYCN. CD532 also can directly interact with AURKA and induces a global conformational shift. CD532 can be used for the research of cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1639009-81-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-112273. | |
| CD532 hydrochloride | CD532 hydrochloride is a potent Aurora A kinase inhibitor with an IC 50 of 45 nM. CD532 hydrochloride has the dual effect of blocking Aurora A kinase activity and driving degradation of MYCN. CD532 hydrochloride also can directly interact with AURKA and induces a global conformational shift. CD532 hydrochloride can be used for the research of cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2926498-81-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-112273A. | |
| CD532 hydrochloride | CD532 hydrochloride is a potent Aurora A kinase inhibitor with an IC50 of 45 nM. CD532 hydrochloride has the dual effect of blocking Aurora A kinase activity and driving degradation of MYCN. CD532 hydrochloride can also directly interact with AURKA and induces a global conformational shift. Synonyms: CD532 (hydrochloride); CD532 hydrochloride; EX-A8075A; HY-112273A; MS-30172; CS-0202740; 2926498-81-7. Grade: 99%. Molecular formula: C26H26ClF3N8O. Mole weight: 558.99. | |
| CD55/DAF human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD58/LFA-3 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| 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. Synonyms: HRF-20 (106-114); Membrane attack complex inhibition factor (106-114). | |
| CD5 human | recombinant, expressed in E. coli, ?80% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD62E/E-Selectin human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD68 human | recombinant, expressed in E. coli, ?85% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD71/TFRC/TFR human | recombinant, expressed in HEK 293 cells, ?92% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD73-IN-1 | CD73-IN-11 is a CD73 inhibitor with an IC50 of ≤316.23 nM for the human enzyme in a cell-free assay. It can be used in cancer treatment. (Extracted from patent WO 2017153952 A1, example 80). Synonyms: VPS34 inhibitor; 5-[N-(2-Cyclopropyl-6-indolyl)sulfamoyl]-2-hydroxybenzamide; CD73 inhibitor 1; Benzamide, 5-[[(2-cyclopropyl-1H-indol-6-yl)amino]sulfonyl]-2-hydroxy-. Grade: ≥98%. CAS No. 2132396-40-6. Molecular formula: C18H17N3O4S. Mole weight: 371.41. | |
| CD73-IN-2 | CD73-IN-2 is a potent CD73 inhibitor with an IC50 of 0.09 nM. Synonyms: ((((2R,3S,4R,5R)-5-((6-chloro-4-(cyclopentylamino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)methyl)phosphonic acid. Molecular formula: C17H25ClN5O7P. Mole weight: 477.84. | |
| CD73-IN-4 | CD73-IN-4 is a potent and selective methylenephosphonic acid CD73 inhibitor with an IC50 of 2.6 nM for human. It has potential in cancer immunology research. Synonyms: 1H-Pyrazolo[3,4-d]pyrimidin-4-amine, 6-chloro-N-cyclopentyl-1-[5-O-(phosphonomethyl)-β-D-ribofuranosyl]-; 6-Chloro-N-cyclopentyl-1-[5-O-(phosphonomethyl)-β-D-ribofuranosyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine. Grade: ≥97%. CAS No. 2216764-29-1. Molecular formula: C16H23ClN5O7P. Mole weight: 463.81. | |
| CD73-IN-5 | CD73-IN-5 is a potent and selective non-nucleotide small molecule CD73 inhibitor with an IC50 of 19 nM. Synonyms: Benzonitrile, 4-[[5-[4-fluoro-1-(1H-indazol-6-yl)-1H-benzotriazol-6-yl]-1H-pyrazol-1-yl]methyl]-. CAS No. 2412019-99-7. Molecular formula: C24H15FN8. Mole weight: 434.43. | |
| CD74/DHLAG human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD74 human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD79B human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD7 human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD80 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD83 human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD84 human | recombinant, expressed in E. coli, ?80% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD84/SLAMF5 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD85J/LILRB1 human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD86 human | recombinant, expressed in E. coli, 0.5 mg protein/mL. Group: Fluorescence/luminescence spectroscopy. | |
| CD87 human | recombinant, expressed in HEK 293 cells, ?92% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CD8B human | recombinant, expressed in E. coli, ?80% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| CDAP | CDAP is an organic cyanylating reagent that can be used for preparation of solid phase affinity reagents, modification of protein thiols and nucleotide delivery. CDAP also activates polysaccharides with a variety of chemical properties. CDAP can be used to prepare conjugate vaccines and other immune reagents [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 59016-56-7. Pack Sizes: 100 mg. Product ID: HY-W012184. | |
| CDBP | CDBP. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4,4'-Bis(carbazol-9-yl)-2,2'-dimethylbiphenyl. Product Category: Organic Light Emitting Diode (OLED). CAS No. 604785-54-8. Molecular formula: C38H28N2. Mole weight: 512.64 g/mol. Product ID: ACM604785548. Alfa Chemistry ISO 9001:2015 Certified. Categories: 4,4'-BIS(9-CARBAZOLYL)-2,2'-DIMETHYLBIPHENYL, CD Projekt. |  |
| 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. Synonyms: H-Thr-Asp-Ser-Gly-Phe-Cys-Leu-Asp-Ser-Pro-Gly-Pro-Leu-Asp-OH. Grade: ≥95%. CAS No. 851538-67-5. Molecular formula: C60H90N14O24S. Mole weight: 1423.52. | |
| CDC25A, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| CDC25B, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| CDC25C, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Cdc25 Inhibitor IV, NSC 95397 (2,3-Bis(2-hydroxyethylthio)-1,4-naphthalenedione, PTP Inhibitor XXIX) | A cell-permeable, para-naphthoquinone that has been reported to inhibit protein tyrosine phosphatase activity, including Cdc25 dual specificity phosphatase (Ki=32nM, 96nM, and 40nM for Cdc25A, -B, and -C, respectively) and blocks G2M transition in murine carcinoma cells. In addition, it is shown to inhibit S100A4 binding to myosin-IIA via covalent modification of cysteine residues, Cys81 and Cys86, in the target binding cleft (IC50=1.8uM). It demonstrates inhibitory activity against S100A4-mediated depolymerization of myosin-IIA filaments. Group: Biochemicals. Grades: Highly Purified. CAS No. 93718-83-3. Pack Sizes: 10mg. Molecular Formula: C??H??O?S?, Molecular Weight: 310.4. US Biological Life Sciences. | Worldwide |
| Cdc2-Like Kinase Inhibitor IV, KH-CB19 | The Cdc2-Like Kinase Inhibitor IV, KH-CB19 controls the biological activity of Cdc2-Like KInase. This small molecule/inhibitor is primarily used for Cell Structure applications. Group: Fluorescence/luminescence spectroscopy. | |
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