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Analysis the Immunoglobulin G and Histidine Interaction by Quartz Crystal Microbalance (QCM) / -Dissipation (QCM-D) (CAT#: STEM-MB-0709-CJ)
Introduction
Immunoglobulin G (IgG) is the most common type. IgG has 4 different subclasses, IgG1— 4. IgG is always there to help prevent infections. It's also ready to multiply and attack when foreign substances get into the body. When you don't have enough, you are more likely to get infections.
Histidine (symbol His or H) is an essential amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated –NH3+ form under biological conditions), a carboxylic acid group (which is in the deprotonated –COO− form under biological conditions), and an imidazole side chain (which is partially protonated), classifying it as a positively charged amino acid at physiological pH. Initially thought essential only for infants, it has now been shown in longer-term studies to be essential for adults also. It is encoded by the codons CAU and CAC.
Principle
The basic principle of QCM is the piezoelectric effect of quartz crystal. Upon an alternating voltage applied to the two poles of the quartz crystal, the quartz crystal of QCM produces mechanical vibration or oscillation. This resonance is greatly sensitive to the thickness of the crystal/electrode system and the frequency of the acoustic frequency. Once the mass on the quartz crystal increases or decreases, the resonance will be disturbed and the resonance frequency of the quartz crystal will change. Thus, the mass variation on the quartz crystal electrode surface is transformed into the frequency variation of the output electric signal of the quartz crystal oscillation and is further transformed into the high-precision data by the computer.
Applications
Immunology/Inflammation; Biochemistry
Procedure
1. Sensor preparation, reduce the risk of damaging or contaminating the sensor surface.
2. Preparation of sample liquids.
3. Places the sensor into the flow cell and ensures perfect alignment.
4. Instant identification of specific sensors by unique ID number.
5. Using quarter turn bayonet type sealed flow cell.
6. Enter the experiment details in the information panel.
7. Display frequency and dissipation in real time.
8. Observe the bubble-free filling through the transparent window.
9. Electronic log file detects all steps in the measurement process.
10. Export and analyze the data.
2. Preparation of sample liquids.
3. Places the sensor into the flow cell and ensures perfect alignment.
4. Instant identification of specific sensors by unique ID number.
5. Using quarter turn bayonet type sealed flow cell.
6. Enter the experiment details in the information panel.
7. Display frequency and dissipation in real time.
8. Observe the bubble-free filling through the transparent window.
9. Electronic log file detects all steps in the measurement process.
10. Export and analyze the data.
Materials
• Sample: Proteins; Microbes; Nucleic Acids; Enzymes; Cells; Polymers; Small molecules; Antibody; Lipids; Virus-like particles (VLPs);
• Equipment: Quartz Crystal Microbalance (QCM) / Quartz Crystal Microbalance-Dissipation (QCM-D)
• Running buffer
• (Optional) PBS solution
• Equipment: Quartz Crystal Microbalance (QCM) / Quartz Crystal Microbalance-Dissipation (QCM-D)
• Running buffer
• (Optional) PBS solution
Notes
1. QCM is an extremely sensitive mass balance that measures nanogram to microgram level changes in mass per unit area.
2. QCM detection limit is approximately 250 ng mL−1, which is similar to that of the existing enzyme-linked immunosorbent assay (ELISA) method.
3. Unlike traditional QCM, the QCM with an added D measures an additional parameter, namely the dissipation factor. so QCM-D has great advantages in providing binding kinetics information by virtue of its label-free breadth of applicability, low cost, and sensing unique mass distribution and viscoelastic behavior aspects of whole-cell responses in real time.
2. QCM detection limit is approximately 250 ng mL−1, which is similar to that of the existing enzyme-linked immunosorbent assay (ELISA) method.
3. Unlike traditional QCM, the QCM with an added D measures an additional parameter, namely the dissipation factor. so QCM-D has great advantages in providing binding kinetics information by virtue of its label-free breadth of applicability, low cost, and sensing unique mass distribution and viscoelastic behavior aspects of whole-cell responses in real time.
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