Heavy-labeled Full-length Proteins

    Recombinant Human RFFL Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 RFFL-5299H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human CDC25C Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 CDC25C-5300H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human SYNPR Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 SYNPR-5301H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human UBXN11 Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 UBXN11-5302H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human TWISTNB Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 TWISTNB-5303H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human PAOX Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 PAOX-5304H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human WDR20 Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 WDR20-5305H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human HAAO Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 HAAO-5306H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human TMEM222 Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 TMEM222-5307H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human SEPTIN5 Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 SEPTIN5-5308H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human COX6C Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 COX6C-5309H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human SPRR2E Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 SPRR2E-5310H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human EPHX1 Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 EPHX1-5311H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human ZFAND5 Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 ZFAND5-5312H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

    Recombinant Human CSH1 Protein, Myc/DDK-tagged, C13 and N15-labeled

    🧪 CSH1-5313H

    Source:  HEK293

    Species:  Human

    Tag:  DDK&Myc

    Conjugation: 

    Protein Length: 

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    Background

    What is isotopic labeling?

    Isotopic labeling is a technique used in chemistry and biology where one or more of the atoms in a molecule is replaced with an isotope of that atom - usually a radioactive or a stable isotope. This is often done to help trace the path of atoms through a chemical reaction or metabolic pathway, or to measure the movement or distribution of a substance within a system. It can also be used to gain information about the structure or function of a molecule.

    What is isotopic labeling

    Due to the costly manners of producing isotopic chemicals and heterologous proteins, an economic 15N/13C isotopic labeling strategy is critically in demand. Stable isotope labeling by amino acids in cell culture (SILAC) is a multiplexing quantitative proteomic method that incorporates isotopically (heavy) labeled amino acids metabolically into the whole proteome.

    Creative BioMart now offers an extensive collection of Mass Spectrometry (MS) standards for 6,000 proteins. Produced in HEK293T cells and labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine, these full-length proteins with appropriate post-translational modifications are ideal identification and quantification standards.

    Advantages

    • Precision: Isotopic labeling allows for a very specific and precise identification and quantification of proteins.
    • Stability: Isotopes are chemically identical to their non-radioactive counterparts and thus do not interfere with the normal function or behavior of the protein.
    • Sensitivity: Isotopic labeling is highly sensitive and can detect even small changes in protein expression or function.
    • Non-destructive
    • Multiple Labeling: With isotopic labeling, multiple isotopes can be incorporated into the same protein, allowing for a detailed study of not only the protein's location but also its interactions with other proteins or molecules.
    • Authentic post-translational modifications
    • High data consistency
    • High reproducibility
    • Identifying the best SRM and MRM transitions
    • Suitable for most types of MS equipment
    • Over 90% incorporation efficiency

    Applications

    Structural Determination: NMR (nuclear magnetic resonance) spectroscopy and other techniques use isotopic labeling to determine the three-dimensional structure of proteins. Specifically labeled isotopes provide greater resolution and clarity in the data.

    Reaction Tracing: Isotopic labeling can track how a protein reacts or metabolizes within a system. For example, a labeled atom could be used to trace the metabolic pathway of a protein in a biological system.

    Quantification: Isotopic labeling can aid in the quantification of proteins in a complex mixture using mass spectrometry.

    Enzyme/Substrate Studies: In enzyme-substrate studies, isotopic labeling helps in identifying the mechanisms and pathways.

    Protein-Protein Interaction: Isotopic labeling is also used to study protein-protein interactions, protein folding, and dynamics.

    Biomolecular research: Isotopic labeling is fundamental for biomolecular research, including drug discovery and development.

    Protein Turnover Studies: It can be used to measure the synthesis and breakdown rates of proteins.

    It also allows for kinetic studies by helping to understand reaction rates and mechanisms.

    Related Resource