Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-009518 |
Molecular Formula: C2[13C][15N]H7NO3 |
Molecular Weight: 107.08 |
Chemical Structure |
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Description | L-Serine-[13C,15N] is a 13C & 15N labelled analogue of L-Serine, which is a non-essential α-amino acid. |
Synonyms | H-Ser-OH-1-13C,15N; (S)-2-Amino-3-hydroxypropanoic acid-1-13C,15N |
Related CAS | 56-45-1 (unlabelled) |
InChI | InChI=1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/i3+1,4+1 |
InChI Key | MTCFGRXMJLQNBG-CQDYUVAPSA-N |
Purity | 98% by CP; 99% atom 13C; 98% atom 15N |
Appearance | White Solid |
L-Serine-[13C,15N], an isotopically labeled iteration of the amino acid serine, is a pivotal tool in scientific inquiry, aiding in the unraveling of metabolic pathways and the exploration of enzyme mechanisms. Here are the key applications of L-Serine-[13C,15N]:
Metabolic Flux Analysis: Utilizing L-Serine-[13C,15N], researchers delve into cellular metabolism by tracing the incorporation of the isotope into metabolic byproducts. This method enables the observation of carbon and nitrogen flow through metabolic pathways, offering deep insights into cellular metabolic states and fluxes. Such analysis is imperative for comprehending diseases like cancer, where metabolic reprogramming plays a crucial role.
Protein Synthesis Studies: By introducing L-Serine-[13C,15N] into proliferating cells, scientists can track the integration of serine into newly synthesized proteins. This practice aids in the exploration of protein turnover rates and synthesis dynamics under varying physiological circumstances. Additionally, it finds application in mass spectrometry-based proteomics, facilitating the identification and quantification of specific proteins within complex mixtures.
Enzyme Mechanism Elucidation: With the assistance of L-Serine-[13C,15N], researchers delve into the intricate mechanisms of serine-dependent enzymes like serine proteases and transaminases. The isotopic labeling technique allows for the tracking of serine throughout enzymatic reactions, shedding light on intermediate states and catalytic mechanisms. This knowledge is instrumental in guiding the development of enzyme inhibitors for therapeutic purposes.
Neurobiology Research: In the realm of neurobiology, L-Serine-[13C,15N] plays a pivotal role in examining serine’s contribution to the central nervous system, particularly in neurotransmitter synthesis and myelin formation. By tracing the isotope within neural cells, researchers uncover the pathways involved in brain metabolism and function, offering valuable insights into neurological diseases and paving the way for targeted treatment approaches.
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