Clinical Chemistry Standards
Genscript Corporation Cardiac Troponin T cTnT Anti
Cardiac Troponin T (cTnT) Antibody (4B6) mAb Mouse
Genscript Corporation MonoRab NT-proBNP 10B11 mA
BNP and NT-proBNP are separated from precursor molecule proBNP via proteolytic processing The BNP and NT-proBNP level in blood are proportional to the severity of cardiac dysfunction They can be used for diagnosis of congestive heart failure (CHF)
DIASYS DIAGNOSTIC SYSTEMS USA LLC DiaSys β-Hydroxybutyrate is an aqueous Standard for use with β-Hydroxybutyrate asays (3x3mL)
DiaSys β-Hydroxybutyrate Standard is an aqueous standard for use in tests for quantitative in vitro determination of β-Hydroxybutyrate. For veterinary or research use only. The standard is used to calibrate β-Hydroxybutyrate assays. DiaSys β-Hydroxybutyrate Standard, both opened and unopened, must be stored refrigerated. Avoid contamination and protect from light. Once opened, DiaSys β-Hydroxybutyrate Standard is stable for 24 months if kept refrigerated and recapped immediatley after use.
YSI 3P LifeScience 1530 L-Lactate Standard, 30 mmol/L (125 mL)
30 mmol/L L-Lactate standard solution for use with YSI 1500, 2300, 2700, 2900 Series and 7100 Analyzers.
Selleck Chemical LLC L-(-)-Glucose S3131-25mg
L-Glucose (L-(-)-Glucose) is an enantiomer of D-glucose L-Glucose promotes food intake while cannot be used by cells as an energy source because it cannot be phosphorylated by hexokinase
Genscript Corporation NT-proBNP 3B42HC
BNP and NT-proBNP are separated from precursor molecule proBNP via proteolytic processing The BNP and NT-proBNP level in blood are proportional to the severity of cardiac dysfunction They can be used for diagnosis of congestive heart failure (CHF)
CAMBRIDGE ISOTOPE LABORATORIES SUPPLEMENTAL CARNITINE REFEREN
NC0949966 SUPPLEMENTAL CARNITINE REFEREN
Medchemexpress LLC 3-Hydroxybutyrate dehydrogenase (3-HBDH) | 9028-38-0 | ≥100 U/mg solid | 100 U
3-Hydroxybutyrate dehydrogenase (3-HBDH) is a mitochondrial enzyme that plays a key role in the ketone body metabolism pathway. It functions as the final enzyme for ketone synthesis in the liver and the initial enzyme for ketone breakdown in extracellular tissues. The absence of 3-Hydroxybutyrate dehydrogenase can lead to inhibited fatty acid oxidation in the liver during fasting in mice, resulting in lipid accumulation and the development of fatty liver.
- Mitochondrial enzyme.
- Key enzyme in ketone body metabolism.
- Involved in both ketone synthesis and breakdown.
- Its absence can lead to fatty liver and severe hypoketosis.