As a normal cellular process, telomere length decreases with age. Telomere length in humans seems to decrease at a rate of 24.8-27.7 base pairs per year. Telomere attrition is a hallmark of the aging process, and its measurement is crucial for understanding the underlying biological mechanisms and developing effective anti-aging interventions. At CD BioSciences, we provide solutions for determining telomere attrition rates in aging, using a range of techniques that offer optimal accuracy and reliability.
Fig .1 Telomere attrition limits the proliferative potential of cells. (McCord RA and Broccoli D, 2008)
To determine telomere attrition rates, it is essential to have high-quality samples. The sample requirements include:
At CD BioSciences, we use a variety of sample types for determining telomere attrition rates, including lymphocytes, whole blood leukocytes, adult bone marrow, fibroblasts, endothelial cells, brain cells, and muscle cells.
Methods | Data processing | Telomere Attrition Rate Determination |
Telomere restriction fragment (TRF) | We measure telomere length using different techniques. The initial measurement represents the starting point for telomere length, while the terminal measurement is obtained from a sample collected at a later time point using the same method. | Telomere attrition rate = (Initial telomere length - Terminal telomere length) / (Initial telomere length) × 100% |
Fluorescence in situ hybridization (FISH) | ||
Quantitative PCR (qPCR) |
CD BioSciences is committed to providing a broad range of telomere loss rate measurement solutions. We offer customized solutions tailored to the specific research question and experimental design, ensuring that the data obtained meets the requirements of our clients. If you are interested in our services, please feel free to contact us or make an online inquiry.
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All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.