Sanshibio 2× SYBR Green qPCR Mix

$15.00

Pengiriman Rp 45 - Gratis lebih dari USD 300

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Deskripsi

Nomor BarangEH003 Spesifikasi:1mL Storage: Simpan pada suhu -20°C

Perkenalan produk

  • Specialized reagent for Real-Time PCR utilizing the SYBR Green I dye-based fluorescence method.
  • Contains an antibody-blocked hot-start enzyme to suppress nonspecific amplification caused by primer dimerization or nonspecific annealing of primers under low-temperature conditions.
  • Enhances the specificity of the amplification reaction.
  • Features high amplification efficiency, strong detection specificity and sensitivity, good stability, and easy operational use.
  • Generates a robust standard curve within a broad quantitative range, memungkinkan kuantifikasi yang akurat.
  • Compatible with a variety of fluorescence quantitative PCR instruments, including those from Applied Biosystems, Eppendorf, Bio-Rad, Roche, and other domestic brands.

Isi produk:

KomponenEH003-02
2× SYBR Green qPCR Mix1ml

Catatan

  • ROX Reference Dye corrects inter-well fluorescence signal errors in certain Real-Time PCR amplification instruments.
  • ROX Reference Dye I is suitable for ABI PRISM 7000/7700/7300/7900HT and Step One Plus Real-Time PCR System.
  • ROX Reference Dye II is compatible with 7500 Real-Time PCR System, 7500 Fast Real-Time PCR System, Stratagene Mx3000P, Mx3005P, and Mx4000.
  • Both ROX Reference Dye I and II should be used at a final concentration of 1× in reactions.
  • Instruments like LightCycler, Thermal Cycler Dice Real Time System II, and Smart Cycler System do not require the use of ROX Reference Dye.

Penyimpanan:

Simpan pada suhu -20°C, dengan umur simpan minimum 12 bulan.

Activity Definition:

Using activated mahi-mahi sperm DNA as template/primer, the activity is defined as 1 satuan (U) of acid-insoluble material incorporated, by taking up 10 nmol of nucleotides within 30 minutes at 74°C.

Kontrol Kualitas:

This product has undergone quality testing and is free from deoxyribonuclease endonuclease activity, deoxyribonuclease exonuclease activity, dan kontaminasi ribonuklease. Host genomic DNA residual content is below 10 salinan.

Product Uses:

Real-time fluorescence Quantitative qPCR (Dye Method) amplifies DNA or cDNA; Absolute Quantitative qPCR; Relative Quantitative qPCR.

Instructions for Use:

  • Allow the required reagents to equilibrate to room temperature until completely dissolved, gently mix thoroughly (do not vortex), use after brief centrifugation to avoid excessive bubble formation and repeated freeze-thaw cycles. If used frequently, store at 4°C. Prepare the PCR reaction mix according to the components pressed down (prepare the reaction mix on an ice box):
Reagen25μL System VolumeKonsentrasi Akhir
2× SYBR Green qPCR Mix12.5μL
Primer I (10mikron)0.5-2.5μL0.2-1.0μM
Primer II (10mikron)0.5-2.5μL0.2-1.0μM
ROX Reference Dye I or ROX Reference Dye II0.5μL or 0.25μL
Templat DNA1-5μL
ddH2HAIHingga 25μL

Catatan:The amounts of each component can be adjusted according to actual needs. The addition of ROX Reference Dye should be determined by users based on the specific model being used.

  • In general, metode dua langkah dapat digunakan untuk reaksi. If amplification is not satisfactory with the two-step method, metode tiga langkah dapat digunakan untuk menyiapkan program reaksi PCR.
Metode/LangkahTwo-step real-time PCRThree-step real-time PCRSiklus
95℃ (Pra-denaturasi)2-5menit2-5menit1
95℃ (Denaturasi)10-20detik10-20detik35-45Siklus
55℃-65℃ (anil)20detik – 1min(Collect fluorescence)10-20detik
72℃ (Perpanjangan)20detik – 1min(Collect fluorescence)
Melting Curve

Catatan: The reaction conditions can be adjusted and optimized according to actual needs. The melting curve program should be selected and adapted based on the amplification instrument’s program being used.

  • After the reaction is complete, analyze the amplification curve and melting curve results. Refer to the Real-Time PCR instrument’s user manual for detailed analysis methods.

Tindakan pencegahan:

  1. Please select appropriate annealing (perpanjangan) temperatures based on primer design, with the primer Tm typically around 60°C. For primers with lower annealing temperatures, a three-step method is recommended. The final concentration of used primers can be adjusted within the range of 0.2-1.0μM. The DNA template concentration can be adjusted according to its concentration.
  2. SYBR Green I dye is a non-specific dye that emits fluorescence upon binding to double-stranded DNA (dsDNA). Namun, it is easily degraded under strong light. Karena itu, when designing primers, it is important to avoid primer dimer formation as much as possible. During usage, prolonged exposure to strong light should be avoided to enhance result accuracy, sensitivity, and specificity.
  3. Increasing the magnesium ion concentration can reduce the inhibitory effect of SYBR Green I on PCR reactions. When optimizing fluorescence PCR reactions using this product, it is advisable to slightly increase the magnesium ion concentration (0.5-3.0mM higher than standard PCR reactions).
  4. Use dedicated areas and pipettes before and after amplification, memakai sarung tangan, dan sering-seringlah mengubahnya. Setelah selesai reaksi PCR, do not open the reaction tubes to minimize contamination of the testing environment with PCR products.

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