Cell Culture Media, Supplements, and Reagents
Miltenyi Biotec, Inc. MACSpep IAV PA (SSLENFRAYV) H2-Db
MACSpep single peptides developed for loading onto MHC multimers using the MHC MACSimer FleX Kits.
This product is subject to the following: Miltenyi Biotec, Inc. Terms and Conditions of Sale For Products and Services
Medchemexpress LLC Didesmethyl cariprazine | 839712-25-3 | MFCD34469127 | 99.6% | 399.36 | C19H28Cl2N4O | 5 MG
Didesmethyl cariprazine is the predominant circulating, orally active metabolite of cariprazine used in pharmacology research to probe dopaminergic and serotonergic mechanisms. It crosses the blood-brain barrier and modulates dopamine and serotonin receptors, making it useful for receptor profiling, metabolism studies, and in vivo pharmacokinetic investigations.
- Orally active, blood-brain barrier permeable compound.
- Partial agonist at D2 and D3 receptors.
- Full agonist at 5-HT1A and antagonist at 5-HT2B.
- Suitable for in vitro receptor pharmacology studies.
- Applicable to in vivo pharmacokinetic and metabolism research.
- Provided as a solid with high reported purity for research use.
![Medchemexpress LLC 1-[3-[3-(4-chlorophenyl)propoxy]propyl]piperidine | 362665-56-3 | 99.7% | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000230583.png-250.jpg)
Medchemexpress LLC 1-[3-[3-(4-chlorophenyl)propoxy]propyl]piperidine | 362665-56-3 | 99.7% | 5 MG
Pitolisant is a potent, selective nonimidazole inverse agonist of the histamine H3 receptor supplied as an analytical standard for research and analytical applications. It is provided as a high-purity liquid suitable for pharmacological studies and method development.
- CAS number 362665-56-3
- IUPAC name 1-[3-[3-(4-chlorophenyl)propoxy]propyl]piperidine
- Molecular formula C17H26ClNO
- Molecular weight 295.85 g/mol
- Purity 99.7% (HPLC)
- Appearance colorless to light yellow liquid
- Available in small mg quantities and as a 10 mM solution in DMSO
- Intended for research use and H3 receptor pharmacology studies
Medchemexpress LLC Ptach | 848354-66-5 | 99.65% | 1 MG
PTACH (NCH-51) is a potent HDAC inhibitor with IC50s of 48 nM, 32 nM, and 41 nM for HDAC1, HDAC4, and HDAC6, respectively. It also significantly inhibits various cancer cells with EC50s ranging from 1.1-9.1 μM and augments HIV-1 production in latently infected OM10.1 cells.
- Potent HDAC inhibitor (HDAC1, HDAC4, HDAC6)
- Exerts growth inhibition against various cancer cells
- Elevates acetylated histone H4 and p21WAF1/CIP1 levels
- Augments HIV-1 production in latently infected OM10.1 cells
Medchemexpress LLC Recombinant human guanylate-binding protein 1 (GBP1) | >95.0% | 10 UG
Recombinant human guanylate-binding protein 1 (GBP1) expressed in HEK293 cells with a C-terminal His tag. GBP1 is a dynamin-family large GTPase involved in innate immunity; it hydrolyzes GTP to GMP and contributes to inflammasome regulation. The product is supplied as a filtered PBS solution, is highly pure, and is provided in microgram quantities for biochemical and cell-based research.
Medchemexpress LLC Ornidazole (levo-) | 166734-83-4 | 98.9% | 10 MG
Ornidazole (Levo-) is the L-isomer (S-enantiomer) of the 5-nitroimidazole compound ornidazole, supplied as an off-white solid for research use. It is used in studies of anti-anaerobic and anti-parasitic activity and has reported effects on neuronal markers such as GAD 65/67 and the Glu/GABA ratio. Product documentation includes a datasheet, COA, and SDS.
- High purity: 98.9%.
- Enantiomerically defined levo (S) isomer for stereospecific research.
- Solid form, convenient small-scale quantity (10 MG).
- Molecular weight 219.63 g/mol; formula C7H10ClN3O3.
- Accompanied by datasheet, COA, and SDS for traceability.
- Suitable for anti-anaerobic, anti-parasitic, and neurochemical research.
American Research Products Inc Rat growth regulated oncogene
Rat growth-regulated oncogene a/melanoma growth stimulating actiVity GROa /MGSA Elisa Kit from CUSABIO Detection Range 125 pg/mL-8000 pg/mL Sensitivity 31 25 pg/mL Sample serum plasma tissue homogenates Method Sandwich
![Medchemexpress LLC N-[4-(4-amino-2-ethylimidazo[4,5-c]quinolin-1-yl)butyl]methanesulfonamide | 532959-63-0 | MFCD30533308 | 99.9% | 361.5 g/mol | C17H23N5O2S | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000215581.png-250.jpg)
Medchemexpress LLC N-[4-(4-amino-2-ethylimidazo[4,5-c]quinolin-1-yl)butyl]methanesulfonamide | 532959-63-0 | MFCD30533308 | 99.9% | 361.5 g/mol | C17H23N5O2S | 25 MG
PF-4878691 is an orally active small-molecule toll-like receptor 7 (TLR7) agonist used in preclinical research to stimulate innate immune responses. It has reported antiviral activity against hepatitis C virus and is applied in oncology and infectious disease research models.
- Orally active TLR7 agonist.
- Stimulates innate immune responses, including interferon production.
- Demonstrated antiviral activity against hepatitis C virus.
- Suitable for preclinical in vitro and in vivo research.
- High chemical purity for research applications.
- For research use only; not for human or clinical use.
Medchemexpress LLC Bafilomycin C1 | 88979-61-7 | 99.9% | 1 MG
Bafilomycin C1 is a macrolide antibiotic isolated from Streptomyces sp. It is a potent, specific, and reversible inhibitor of vacuolar-type H+-ATPases (V-ATPases). Bafilomycin C1 inhibits the growth of gram-positive bacteria and fungi, induces cell apoptosis, and is used for studying hepatocellular carcinoma (HCC).
- Potent, specific, and reversible inhibitor of V-ATPases
- Isolated from Streptomyces sp.
- Inhibits gram-positive bacteria and fungi
- Induces cell apoptosis
- Used for studying hepatocellular carcinoma (HCC)
- Induces G0/G1 cell-cycle arrest
- Induces mitochondrial-mediated apoptosis
- 99.9% purity
Medchemexpress LLC Bio-THZ1 | 1604811-14-4 | 98.1% | 10 MG
bio-THZ1 is a biotinylated version of THZ1 that irreversibly binds to CDK7. THZ1 is identified as a selective and potent covalent CDK7 inhibitor with an IC50 of 3.2 nM.
- Biotinylated version of THZ1
- Irreversibly binds to CDK7
- Selective and potent covalent CDK7 inhibitor
- IC50 of 3.2 nM
Medchemexpress LLC KPLH1130 | 906669-07-6 | 99.9% | 50 MG
KPLH1130 is a pyruvate dehydrogenase kinase (PDK) inhibitor. It potently inhibits M1 macrophage polarization by reducing pro-inflammatory cytokines, decreasing M1 phenotype markers (HIF-1α, iNOS), and lowering nitric oxide (NO) production. It prevents the reduction of mitochondrial oxygen consumption rate (OCR) induced by inflammatory stimuli and improves glucose tolerance in HFD-fed mice. It can be used for the study of obesity-associated metabolic disorders and other inflammatory conditions.
- Potently inhibits M1 macrophage polarization
- Reduces pro-inflammatory cytokines
- Decreases M1 phenotype markers (HIF-1α, iNOS)
- Lowers nitric oxide (NO) production
- Prevents reduction of mitochondrial oxygen consumption rate (OCR)
- Improves glucose tolerance in HFD-fed mice
- Useful for studying obesity-associated metabolic disorders
- Useful for studying inflammatory conditions
Medchemexpress LLC Neomycin C (hexaacetate) | 66-86-4 | 97.1% | 1 MG
Neomycin C hexaacetate is an impurity of Neomycin and a stereoisomer of Neomycin B. It exhibits in vitro antimicrobial activity against Staphylococcus epidermidis and Staphylococcus aureus, and can be used for the research of bacterial infection.
- Exhibits in vitro antimicrobial activity against Staphylococcus epidermidis and Staphylococcus aureus.
- Useful for bacterial infection research.
- Molecular weight of 974.96.
- Chemical formula C35H70N6O25.
- Solid appearance.
- White to off-white color.
![Medchemexpress LLC 2-[4-[(4-methoxyphenyl)methoxy]-phenyl]acetonitrile | 1016535-83-3 | MFCD09929139 | 98.1% | 241.26 g/mol | C15H12FNO | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000299030.png-250.jpg)
Medchemexpress LLC 2-[4-[(4-methoxyphenyl)methoxy]-phenyl]acetonitrile | 1016535-83-3 | MFCD09929139 | 98.1% | 241.26 g/mol | C15H12FNO | 10 MG
Oct3/4-inducer-1 is a small-molecule activator that promotes expression, stabilization, and transcriptional activity of the Oct3/4 (Oct4) transcription factor in human somatic cells. Supplied for research use only, it is used in studies of pluripotency and cellular reprogramming.
- Promotes expression and stabilization of Oct3/4.
- Enhances Oct3/4 transcriptional activity in diverse human somatic cells.
- Provided as a solid with high reported purity (98.1%).
- Soluble in DMSO at 100 mg/mL for preparation of stock solutions.
- Suitable for studies of pluripotency and induced pluripotent stem cell formation.
- Recommended storage: solid at 4°C; aliquots in solution at -80°C for long-term storage.
American Research Products Inc Rat Insulin like growth factor
Rat Insulin-like growth factor binding protein 1 IGFBP-1 ELISA Kit from CUSABIO Detection Range 15 6 pg/mL-1000 pg/mL Sensitivity 3 9 pg/mL Sample serum plasma cell culture supernates tissue homogenates Method Sandwich
American Research Products Inc Rabbit basic fibroblast growth
Rabbit basic fibroblast growth factor bFGF ELISA Kit from CUSABIO Detection Range 7 8 pg/mL-500 pg/mL Sensitivity 1 95 pg/mL Sample serum plasma tissue homogenates Method Sandwich