Benzoxazines
Cell Signaling Technology CD14 (D7A2T) Rabbit mAb (Alexa Fluor(R) 555 Conjugate) 100 ul
CD14 (D7A2T) Rabbit mAb (Alexa Fluor(R) 555 Conjugate) 100 ul
Apexbio Technology LLC Resazurin sodium salt 62758-13-8 1g
Resazurin sodium salt (62758-13-8) is a cell-permeable fluorometric redox indicator It is designed to assess cellular metabolic activity by measuring the redox potential within viable cells Resazurin sodium salt exerts its biological activity primarily through reduction by intracellular enzymes converting from a non-fluorescent compound to the fluorescent dye resorufin In cell-based studies previously published data demonstrated IC50 values in mammalian cell lines typically in the micromolar range upon prolonged incubation periods Based on these pharmacological properties resazurin sodium salt holds research potential in evaluating cell proliferation metabolic state cytotoxicity and viability assays in high-throughput screening fluorescence microscopy and flow cytometry
TARGETMOL CHEMICALS INC E6446 DIHYDROCHLORIDE 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. E6446 dihydrochloride is a novel synthetic antagonist for nucleic acid-sensing TLRs; potently suppressed DNA stimulation of HEKTLR9 cells with IC50 of 10 nM. purity: 99%
Cell Signaling Technology Arginase-1 D4E3Mtm XPR R
Arginase-1 (D4E3M(tm)) XP(R) Rabbit mAb (Alexa Fluor(R) 647 Conjugate) 100 ul
Cell Signaling Technology CD69 H1.2F3 Hamster mAb FIT
CD69 (H1.2F3) Hamster mAb (FITC Conjugate) 100 ug
TARGETMOL CHEMICALS INC IKK 16 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. IKK 16 (IKK Inhibitor VII) is a selective I(kappa)B kinase (IKK) inhibitor for IKK-2 IKK complex and IKK-1 with IC50 of 40 nM 70 nM and 200 nM respectively. purity: 99%
TARGETMOL CHEMICALS INC VT103 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. VT103 is an orally active and selective inhibitor of TEAD1 protein palmitoylation and is an analog of VT101. VT103 has potential antitumor activity by inhibiting YAP/TAZ-TEAD-promoted gene transcriptionment blocking TEAD auto-palmitoylation and blocking the interaction between YAP/TAZ and TEAD.VT103 can be used in the study of HER2-positive breast cancer prostate cancer and triple-negative breast cancer. purity: 98%
TARGETMOL CHEMICALS INC MK-2461 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. MK-2461 is a novel ATP-competitive multitargeted inhibitor of activated c-Met with a mean IC50 of 2.5 nM. purity: 99%
Cell Signaling Technology Cleaved Caspase-8 Asp387 D5
Cleaved Caspase-8 (Asp387) (D5B2) XP(R) Rabbit mAb (PE Conjugate) 100 ul
Cell Signaling Technology Ubiquitin P4D1 Mouse mAbHR
Ubiquitin (P4D1) Mouse mAb(HRP Conjugate) 100 ul
TARGETMOL CHEMICALS INC CALCIFEDIOL 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Calcifediol (U 32070E)(Ki of 3.9 uM) a major circulating metabolite of vitamin D3 works as a competitive inhibitor. It (ED50=2 nM)also inhibits PTH secretion and mRNA. purity: 99%
TARGETMOL CHEMICALS INC MI-503 5MG
Also available in 2 mg 10 mg 25 mg 50 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. MI-503 is a highly effective and orally bioavailable inhibitor of the menin-mLL interaction. purity: 99%
TARGETMOL CHEMICALS INC DBET1 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. dBET1 is a hybrid molecule that combines (+)-JQ1 and thalidomide. It induces cereblon-dependent BET protein degradation in vitro (EC50 430 nM) and induces apoptosis. purity: 99%
TARGETMOL CHEMICALS INC PGD2-IN-1 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. PGD2-IN-1 (PGD2-inhibitor) is an effective DP receptor antagonist (IC500.3 nM) a compound that can inhibit prostaglandin D2 (PGD2) signaling. PGD2-IN-1 specifically targets and regulates the activity of PGD2 receptors or enzymes involved IN PGD2 synthesis or metabolism. purity: 98%