Benzoxazines
Cell Signaling Technology Tom20 (D8T4N) Rabbit mAb (HRP Conjugate) 100 ul
Tom20 (D8T4N) Rabbit mAb (HRP Conjugate) 100 ul
TARGETMOL CHEMICALS INC ATC 0175 HYDROCHLORIDE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. ATC 0175 hydrochloride is an orally active melanocyte concentrating hormone 1 receptor antagonist that is potent and selective. ATC 0175 hydrochloride has affinity for MCH1R MCH2R MCH1 5-HT2B receptors and 5-HT1A receptors with IC50s of 13.5 nM >10000 nM 13 nM 9.66 nM and 16.9 nM respectively. ATC 0175 hydrochloride exhibits antidepressant and anxiolytic effects in animal models. aTC 0175 can be used to study depression and/or anxiety disorders. purity: 99%
Aat Bioquest 6CR6G SE 6Carboxyrhodamine
6CR6G SE [6Carboxyrhodamine 6G succinimidyl ester] *Single isomer*
Aat Bioquest Caliber Fluor™ 580
Caliber Fluor™ 580 is an extremely stable fluorophore that has its absorption and fluorescence independent of pH change from pH 3 to 10.
Aat Bioquest Cyanine 7 azide [equivalent to Cy7 azide]
A variety of cyanine 7 (Cy7) dyes has been used to label biological molecules for fluorescence imaging and other fluorescence-based biochemical analysis.
AdipoGen Resorufin
Chemical. CAS 635-78-9. Formula C12H7NO3. MW 213.19. Resorufin is a stable red fluorophore standard widely used in biochemical and molecular biology research. It is used in enzyme assay systems e.g. Amplex Red and as an indicator of cell viability in assays. Resorufin represents the reduced dye formed from Amplex Red reaction or resazurin reductions. One common application of resorufin is in the measurement of mitochondrial activity. When cells are metabolically active, they can reduce resazurin to resorufin, producing a measurable fluorescent signal. This property makes resorufin a valuable tool in various research applications, such as assessing cell health, drug screening, and enzyme activity studies. It is unstable in the presence of thiols such as dithiothreitol DTT and 2-mercaptoethanol. This compound can be used as a standard for enzyme substrates whose end product is resorufin.
TARGETMOL CHEMICALS INC FEN1-IN-3 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. FEN1-IN-3 is a human flap endonuclease-1 ( hFEN1 ) inhibitor that stabilizes hFEN1 with an EC 50 of 6.8 uM . purity: 98%
TARGETMOL CHEMICALS INC ML-210 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ML-210 (CID 49766530) is a selective RAS and covalent glutathione peroxidase 4 (GPX4) inhibitor(GPX4 EC50 30 nM) with anti-cancer activitypurity: 97%
TARGETMOL CHEMICALS INC JD-5037 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. JD-5037 is a novel peripherally restricted CB1R antagonist with an IC50 of 1.5 nM. purity: 98%
TARGETMOL CHEMICALS INC PIM1/AKK1-IN-1 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. Pim1/AKK1-IN-1 (LKB1/AAK1 dual inhibitor) is a potent multi-kinase inhibitor with Kd values of 35 nM/53 nM/75 nM/380 nM for Pim1/AKK1/MST2/LKB1 respectively and also inhibits MPSK1 and TNIK. purity: 98%
TARGETMOL CHEMICALS INC SANGGENON C 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 1. Sanggenon C (Sanggenone C) inhibits tumor cellular proteasomal activity and cell viability via induction of cell cycle arrest and cell death inhibiting the proteasome function. 2. Sanggenon C and O inhibited NO production and iNOS expression by suppressing NF-(kappa)B activity and I(kappa)B(alpha) activation; inhibited TNF-alpha -stimulated PMN-HSC adhesion and expression of VCAM-1 by suppressing the activation of NF-kappaB. purity: 98%
TARGETMOL CHEMICALS INC BLU0588 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. BLU0588 is a selective PRKACA inhibitor. BLU0588 inhibits PRKACA catalytic activity with a half-maximal inhibitory concentration (IC50) of 1 nM.