• StarLighter Probe qPCR Master Mix (Universal)
  • StarLighter Probe qPCR Master Mix (Universal)

StarLighter Probe qPCR Master Mix (Universal)

No.FS-Q2002/FS-Q2001-S

StarLighter Probe qPCR Mix (Universal) This universal probe-based kit enables rapid, real-time quantitative analysis of DNA samples from a variety of sources. Based on the high-performance hot-start engineered Taq DNA polymerase and optimized buffer, the kit effectively reduces nonspecific amplification and significantly increases qPCR efficiency, making it suitable for highly sensitive qPCR assays. The kit boasts a wide quantification range, enabling accurate quantitative and qualitative analysis of target genes and SNP detection. It offers excellent reproducibility, high reliability, and compatibility with a wide range of qPCR probes.

Item No./Specifications/Price:
FS-Q2002/5 ml, 4*1.25 ml/box/¥1200
FS-Q2001-S/1 ml, 1 tube/box/¥300
  • StarLighter Probe qPCR Master Mix (Universal)

Product Description

StarLighter Probe qPCR Mix(Universal)
StarLighter Probe qPCR Master Mix (Universal)


Product Advantages
  • Strong amplification specificity and reliable data results
  • High GC template amplification ability
  • High amplification efficiency and early Ct value
  • High signal-to-noise ratio and high sensitivity for low copy detection

Product Application
  • Gene expression analysis
  • SNP and allele typing
  • Validation of sequencing and microarray results

Product components


Product Performance
  • Strong amplification specificity and reliable data results

Fig.1 Comparison of the accuracy of quantitative results of different reagents

StarLighter Probe qPCR Mix (Universal) and reagents from other suppliers were used to quantify the ApoE gene (ApoE2 and ApoE3) using a human genome containing the ApoE3 genotype (without the ApoE2 genotype) as a template (ARMS-qPCR was used to genotype the two ApoE genotypes, ApoE2 and ApoE3). The StarLighter reagent effectively amplified the ApoE3 genotype (high GC content), while the reagent from supplier K failed to amplify the ApoE gene (amplified fragment length, 197 bp, GC content, 71%).

  • Strong amplification ability for high GC templates


Tab.1 Quantification using StarLighter Probe qPCR Mix (Universal) reagent and the human genome carrying ApoE3 gene isoforms as template. Compared with Supplier K, the StarLighter Probe qPCR Mix can detect well, while Supplier K cannot detect.


Fig.2 Comparison of the results of quantification of high GC content fragments using different reagents.

Using the human genome as a template, the ApoE3 gene was amplified at template concentrations of 50 ng, 5 ng, 0.5 ng, and 0.05 ng, resulting in a 197 bp amplified fragment with a GC content of 71%. StarLighter Probe qPCR Mix (Universal) reagents achieved efficient amplification, while no amplification was achieved using Supplier K (Ct>45).
  • High amplification efficiency and good linear range

Comparing the quantification of the internal reference gene Actin with StarLighter Probe qPCR Mix (Universal) and Supplier K, the Ct value was earlier than that of Supplier K and the amplification efficiency was better.

Fig.3 Comparison of quantitative results of different reagents for continuous gradient dilution template

Using the human genome as a template, the internal reference gene Actin was quantified at template concentrations of 50 ng, 5 ng, 0.5 ng, and 0.05 ng, respectively. The amplified fragment length was 179 bp. The StarLighter Probe qPCR Mix (Universal) effectively amplified the Actin gene, with improved amplification efficiency and R2 values compared to competing products. Ct values were approximately 1-1.5 cycles ahead of the supplier's K value.
  • High sensitivity, suitable for low copy detection

Fig.4 StarLighter Probe qPCR Mix quantitative results of low-copy samples

Using the human genome as a template, the starting concentration was 100 ng, followed by a 5-fold serial dilution. qPCR quantification was performed using StarLighter Probe qPCR Mix (Universal) reagent. The reference gene Actin and the target gene ApoE3 were effectively amplified at a template concentration as low as 0.032 ng, with a good linear relationship between the logarithmic value of the starting template amount and the corresponding Ct value.

  • High stability

Fig.5 StarLighter Probe qPCR Mix stability test results

Reagent A was repeatedly frozen and thawed at least 30 times; reagent B was stored at 37°C for up to 5 days; reagent C was stored at room temperature for up to 28 days; and reagent D was stored at 4°C for up to 43 days. Actin and ApoE genes were quantified using human DNA as a template, and no significant decrease in signal intensity or delay in Ct values was observed (this experiment was performed on a Thermo Q6 instrument).


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