Protein Purification
Hampton Research SOL & STABILITY #67 (F7)
HR2-072-67/Solubility & Stability #67 (F07), 1.0 ml - 500 mM DL-Malic acid pH 7.0. Please note items from this supplier are non-returnable.
Hampton Research SOL & STABILITY #74 (G2)
HR2-072-74/Solubility & Stability #74 (G02), 1.0 ml - 700 mM Sodium phosphate monobasic monohydrate, 1,300 mM Potassium phosphate dibasic. Please note items from this supplier are non-returnable.
Medchemexpress LLC HY-100612 10mg Medchemexpress, T16Ainh-A01 CAS:552309-42-9 Purity:>98%
Medchemexpress, HY-100612 10mg T16Ainh-A01 CAS:552309-42-9 T16Ainh-A01, an aminophenylthiazole, is a potent transmembrane protein 16A (TMEM16A) inhibitor, inhibiting TMEM16A-mediated chloride currents with an IC50 value of ~1 µM. TMEM16A (ANO1) functions as a calcium-activated chloride channel (CaCC). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC RIP1 kinase inhibitor 1 | 2095515-38-9 | 100.0% | 461.90 | 50 MG
RIP1 kinase inhibitor 1 (compound 22) is a highly potent, orally available, and brain-penetrating RIP1 kinase inhibitor (pKi=9.04). It strongly suppresses necroptotic cell death and phosphorylation of MLKL (pMLKL) in human colorectal adenocarcinoma HT-29 cells (necroptosis, IC50=2 nM; pMLKL, IC50=1.3 nM) as well as mouse L-cells NCTC 929 (necroptosis, IC50=15 nM; pMLKL, IC50=2.7 nM). This inhibitor is designed for high-speed applications.
- Highly potent and orally available
- Brain-penetrating RIP1 kinase inhibitor
- Strongly suppresses necroptotic cell death
- Inhibits phosphorylation of MLKL (pMLKL)
- Effective in human colorectal adenocarcinoma HT-29 cells
- Effective in mouse L-cells NCTC 929
Hampton Research STOCKOPT TRICINE #12 PH 8.5
HR2-253-12/StockOptions Tricine #12, 1.0 M Tricine pH 8.5, 185 ml. Please note items from this supplier are non-returnable.
Ubpbio A covalent inhibitor of 3CL protease. A component of Paxlovid used for the treatment of COVID 19. CAS# 26288280-40-8, > 99% purity
PF-07321332 is an orally active covalent inhibitor of the 3C-like protease by direct binding of the catalytic cysteine 145. 3CL protease cleaves polyproteins 1a and 1ab of SARS-CoV-2, a step required for reproduce the virus. The PF-07321332/ritonavir combination drug (trade name Paxlovid) is efficient for the treatment of COVID-19 as, in November 2021, Pfizer announced phase 2/3 clinal trial results that the drug treatment reduced 89% in hospitalizations when given within three days after symptom onset. This product is for research use only.
Ubpbio A reversible inhibitor of serine and cysteine proteases. CAS# 103476-89-7, > 98% purity
Leupeptin hemisulfate (Ac-Leu-Leu-argininal) is a reversible inhibitor of serine and cysteine proteases, including plasmin, trypsin, papain, kallikrein, calpain and cathepsin B. A widely used protease inhibitor and typical working concentration is 10 - 100 μM.
Supply Solutions Protease Inhibitor Cocktail, MFCD00677817, 5mL
For use with mammalian cell and tissue extracts, DMSO solution
Echelon Biosciences Research Labs PI(3,4,5)P2 PIP Beads 1 mL
PI(3,4,5)P3 PIP BeadsTM are composed of agarose with 10 nanomoles of bound PI(3,4,5)P3 per mL of beads, enough for several protein binding experiment. Each 1 mL order of PIP Beads includes a small amount of control beads. Larger quantities of Control Beads are also available for purchase. This item is non returnable