Human Telomere Length Quantification qPCR Assay Kit （Relative ）
Advantages
Get results quickly,saving 50% of time
Optimized ready-to-use master mix for rapid PCR reactions.
Accurate detection of various starting amounts of templates,stable amplification,and highly reproducible
quantitative results.
Balanced ration of K+and NH4
+ ions,and independent ROX reference Dye packaging,suitable for all real-time
PCR instruments.
Introduction
Telomere (Telomere) is a DNA sequence at the end of a eukaryotic cell chromosome composed of multiple repeating
nucleotide elements (TTAGGG) in tandem. In addition to providing a buffer for non-transcribed DNA, it can also protect
the end of the chromosome from fusion and Degenerate, protect chromosome structure stability and genetic integrity.
Telomere is the most important and accurate indicator of a person's aging rate. Its initial length is determined by
genetic and environmental factors, and will decrease over time. Studies have shown that telomere length is closely
related to DNA repair, aging, apoptosis, and tumorigenesis. Therefore, accurate and repeatable measurement of
telomere length is particularly important for researchers. This product mainly uses relative quantitative qPCR to
directly compare the average telomere length of the sample, that is, the copy number ratio (T/S) of the telomere
repeat sequence (Tel) and the genome single copy gene (SCR) copy number (T/S) is used as the telomere relative
length. Single-copy gene primers (SCR) specifically recognize and amplify the 78bp long region on human chromosome
11.
The primer set in the kit has passed the test to ensure: (1) efficient and reliable quantification; (2) no non-specific
amplification. Each set of primers has been verified by amplification curve efficiency (E>98%, R2>0.99), melting curve
analysis and gel electrophoresis verification.
SYBR Green PCR SuperMix can perform specific and sensitive detection in a wide range, and is suitable for
standard and rapid thermal cyclers. The SYBR Green I dye in the master mix can analyze multiple target nucleic acids
without the need to synthesize sequence-specific probes. Antibody method hot-start Taq enzyme can effectively
inhibit the amplification caused by primer non-specific annealing. At the same time, the PCR formula is optimized,
suitable for the amplification of low-concentration templates, so that quantitative PCR can obtain a good standard
curve in a wide quantitative area.
Информация для заказа
| Область использования: | Производство: | Puda Scientific |
| Метод: | |
| Объем: | 100 тестов |
| Кат. номер: | PD-PCR-02522 |
| Цена (с НДС 20%): | по запросу | В корзину  |
Наименование: Human Telomere Length Quantification qPCR Assay Kit （Relative ）.
Примечание: |
