Protein Purification
Cayman Chemical BTYNB IMP1 InhIbItr 25mg
An IMP1 inhibitor (IC50 = 5 μM for IMP1 binding to c-Myc mRNA); downregulates c-Myc and β-TrCP1 mRNA and reduces IMP1 protein levels in SK-MEL-2 and IGROV-1 cells; inhibits proliferation of IMP1-positive ES-2, IGROV-1, and SK-MEL-2 cells (IC50s = 2.3, 3.6, and 4.5 μM, respectively); inhibits anchorage-independent growth of SK-MEL-2 cells at 10 μM
Cayman Chemical USP7-USP47 InhIbItr 10mg
A dual inhibitor of USP7 and USP47 (IC50s = 0.42 and 1 μM, respectively); selective for USP7 and USP47 over USP2, USP5, USP8, USP21, USP28, caspase-3, and cathepsin B (IC50s = >31.6 μM); inhibits the growth of HCT116 cells (EC50 = 7.6 μM)
ACROBiosystems Human BCMA 2.5mg
ActiveMax Human BCMA uBeads premium grade (for cells) are uniform superparamagnetic beads of 5.5 µm with streptavidin on its surface and coupled with biotinylated Human BCMA Protein expressed from human 293 cells (HEK293) and contains AA Met 1 - Ala 54 (Accession # Q02223-1).
Bioworld SEPAROPOREAGAROSE) 6B
A high gel strength bioagarose matrix for gel filtration and coupling of affinity ligands suitable for analytical and preparative protein purifications. Larger volumes available at more competitive prices(enquie). Specifications: Parti...
Medchemexpress LLC NSC668394 100mg | 382605-72-3 | 452.1 g/mol | C17H12Br2N2O3 | 100 MG
NSC668394 is a small-molecule inhibitor of ezrin Thr567 phosphorylation offered for research use. It is supplied as an orange to red solid with molecular formula C17H12Br2N2O3, molecular weight 452.1 g/mol, and reported purity of 99.31%. The compound is available in multiple pack sizes, including 100 MG, and has recommended storage conditions for powder and solutions to preserve stability.
- Inhibits ezrin Thr567 phosphorylation for cellular and biochemical studies.
- High reported purity (99.31%) suitable for research applications.
- Orange to red solid physical form for easy handling.
- Molecular weight 452.1 g/mol; formula C17H12Br2N2O3.
- Available in multiple pack sizes, including 100 MG.
- Powder storage: -20°C for long-term stability; in solvent: -80°C recommended for extended storage.
- For research use only; not for human or veterinary use.
Hampton Research HR2-943-10/StockOptions MES #10 pH 6.1, 185 ml
HR2-943-10/StockOptions MES #10 pH 6.1, 185 ml. Please note items from this supplier are non-returnable.
Zymo Research Corporation MIP Buffer, 20 ml
The MIP Buffer provides optimal conditions for the antibody/Protein A/DNA complex formation. Highlights: Sold separately or as part of the Methylated-DNA IP Kit (D5101). Storage temperature: 0°C to room temperature.
Cayman Chemical CBF InhIbItr 10mg
A small molecule that binds to CBFβ and inhibits its association with Runx1 (IC50 = 3.2 µM); blocks CBFβ-Runx1 interactions in ME-1 cells, acute myeloid leukemia cells harboring dysfunctional CBF, reducing proliferation without toxicity
Epigentek Inc EpiQuik Total Histone Extraction HT Kit (192 extractions)
The EpiQuik Total Histone Extraction HT Kit provides a simple and high throughput microplate method for extracting histone proteins used for a variety of applications, which include histone modifications such as acetylation, methylation, and sumoylation. This kit is also specifically designed to meet the requirements of histone extracts used in EpiQuik histone quantification assays. The kit can be used to directly extract histones from mammalian cells cultured in a 96-well plate. The EpiQuik Total Histone Extraction HT Kit has the fastest procedure available on the market, allowing completion within 60 minutes.
Selleck Chemical LLC Tadalafil 50mg 171596-29-5 IC351
Tadalafil (IC351) is a PDE-5 inhibitor with IC50 of 1.8 nM in a cell-free assay. Tadalafil is at least 9000 times more selective for PDE5 than most of the other families of PDEs, with the exception of PDE11. It can partial inhibits PDE11 *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Cayman Chemical GPX4 InhIbItr 17 5mg
A GPX4 inhibitor and ferroptosis inducer; inhibits GPX4 activity by 49.16% at 1 µM; increases the production of ROS and levels of MDA in OS-RC-2 cells 0.5 µM; induces ferroptosis in HT-1080 cells (IC50s = 0.007 and 1.486 µM, in the absence and presence of ferrostatin-1, respectively); reduces tumor volume and intratumoral GPX4 levels in an OS-RC-2 mouse xenograft model 20 mg/kg
Cayman Chemical Syk InhIbItr IIhydrochlorI 5mg
A cell-permeable, selective, and reversible inhibitor of Syk (IC50 = 41 nM); prevents FcεRI-mediated 5-HT release in RBL-2H3 cells in vitro (IC50 = 460 nM) and inhibits passive cutaneous anaphylaxis reactions in mice (ID50 = 13.2 mg/kg, s.c.)