Carbohydrates
Cell Signaling Technology Phospho-ROS1 (Tyr2274/2334) (E8F5J) Rabbit mAb 100 ul
Phospho-ROS1 (Tyr2274/2334) (E8F5J) Rabbit mAb 100 ul
Medchemexpress LLC Beta-glucuronidase (helix pomatia) | 9001-45-0 | 100 KU
Beta-glucuronidase (helix pomatia) is a glycosyl hydrolase that hydrolyzes β-glucuronic acid and sulfate esters in urine and other biological fluids, releasing β-glucuronate.
- Functions as a glycosyl hydrolase
- Hydrolyzes β-glucuronic acid
- Hydrolyzes sulfate esters
- Active in urine and other biological fluids
- Releases β-glucuronate
Medchemexpress LLC D-ribose (mixture of isomers) | 50-69-1 | MFCD00135453 | 98.0% | 150.13 g/mol | C5H10O5 | 500 MG
D-Ribose (mixture of isomers) is a research-grade endogenous sugar supplied as a high-purity solid for use in biochemical, enzymatic, and metabolic studies. The material is suitable for cell supplementation and analytical assays, and is offered with supporting documentation including SDS and COA.
- High purity (98.0%).
- Chemical formula C5H10O5; molecular weight 150.13 g/mol.
- Suitable for metabolic and enzymatic assays.
- Available in lab pack sizes, including 500 mg.
- Provided with SDS, COA, and analytical data.
Medchemexpress LLC Phospholipase D, Streptomyces chromofuscus (PLD) | 9001-87-0 | 5 KU
Phospholipase D, Streptomyces chromofuscus (PLD) is an enzyme of the phospholipase superfamily, found across various life forms and frequently used in biochemical research. It catalyzes the hydrolysis of phosphodiester bonds in glycerophospholipids, yielding phosphatidic acid and soluble choline. This enzyme is implicated in various disease-related processes. This product is an enzyme preparation derived from natural strains through deep liquid fermentation, containing highly active phospholipase.
- Catalyzes hydrolysis of phosphodiester bonds in glycerophospholipids.
- Produces phosphatidic acid and choline.
- Specifically catalyzes hydrolysis of phosphatidyl diester bond at the end of phosphatidylcholine.
- Enzyme activity is ≥50000 U/mL.
- Effective temperature range 35°C-55°C, optimum 40°C-50°C.
- Effective pH range pH4.0-7.5, optimum pH 5.0-6.0.
- Soluble in H2O at ≥ 100 mg/mL.
Cambridge Isotope Laboratories D-Glucose (U-13C6 99%) microbiological/pyrogen tested 1 g
D-Glucose (U-13C6 99%) microbiological/pyrogen tested 1 g
Selleck Chemical LLC Methotrexate disodium S5097-1g
Methotrexate sodium an analog of folic acid is a nonspecific inhibitor of the dihydrofolate reductase(DHFR) of bacteria and cancerous cells as well as normal cells It forms an inactive ternary complex with DHFR and NADPH Methotrexate (MTX) induces apoptosis
Cell Signaling Technology IGF-I Receptor beta (D4O6W) Rabbit mAb 20 ul
IGF-I Receptor beta (D4O6W) Rabbit mAb 20 ul
Medchemexpress LLC L-mannose | 10030-80-5 | MFCD00136021 | 98.0% | 180.16 g·mol⁻¹ | C6H12O6 | 50 MG
L-Mannose is a naturally occurring monosaccharide (CAS 10030-80-5) supplied as a solid reagent for biochemical research. It has formula C6H12O6, molecular weight 180.16 g·mol⁻¹, and is commonly used as a substrate in enzymatic assays and stereochemical carbohydrate studies.
- Monosaccharide reagent suitable for enzymatic assays.
- Purity 98.0% for reproducible results.
- Solid form, easy to weigh and store.
- Useful as a substrate for mannose-6-phosphate isomerase studies.
- Available in small pack sizes for research-scale use.
Cambridge Isotope Laboratories D-Glucose (1 2 3 4 5 6 6-D7 97-98%) 10 g
D-Glucose (1 2 3 4 5 6 6-D7 97-98%) 10 g
Medchemexpress LLC Sucralose (Standard) | 56038-13-2 | 397.63 | 25 MG
Sucralose (Standard) is the analytical standard of Sucralose, intended for research and analytical applications. It is a non-nutritive artificial sweetener and sugar substitute that can activate a conserved neural fasting response, exerting an appetite-stimulating effect in rodents.
- Serves as an analytical standard
- Used in qualitative, quantitative, and methodological research experiments
- Applicable for HPLC, GC, and MS
- Non-nutritive artificial sweetener
- Sugar substitute
- Can stimulate appetite in rodents by activating a neural fasting response