Hifair™ AdvanceFast 1st Strand cDNA Synthesis Kit (No Dye) is a rapid reverse transcription kit developed based on the Hifair™ III 1st Strand cDNA Synthesis Kit (No Dye), suitable for PCR amplification and RT-qPCR experiments. Compared to the Hifair™ III 1st Strand cDNA Synthesis Kit (No Dye), it boasts stable detection rates, specificity, and yield assurance, with the total reverse transcription time potentially reduced to less than 6 minutes, significantly shortening experimental duration. The kit includes gDNA Digester Mix, which can eliminate genomic DNA contamination remaining in the RNA template, ensuring more reliable subsequent results. The kit provides two types of cDNA synthesis primers: Random Primers N6 and Oligo (dT)18. Users can choose between Random Primers N6, Oligo (dT)18, or Gene Specific Primers as reverse transcription primers according to their needs. The synthesized single-stranded cDNA product can be directly used for subsequent PCR or qPCR reactions. Specifications Cat.No. 11150ES10 / 11150ES60 Size 10 T/100 T Components Components No. Name 11150ES10 11150ES60 11150-A 4× Hifair™AdvanceFast SuperMix (No Dye) 50 μL 500 μL 11150-B 5×gDNA Digester Mix 20 μL 200 μL 11150-C Random Primers (50 μmol/L) 20 μL 200 μL 11150-D Oligo d(T)18 Primers (50 μmol/L) 20 μL 200 μL 11150-E RNase-free Water 200 μL 2×1 mL Storage This product should be stored at -25~-15℃ for 1 year. Instructions If the experiment requires the removal of residual genomic DNA 1)gDNA Digestion In a RNase-free centrifuge tube, prepare the following mixture and gently pipette to mix well. Incubate at 42℃ for 2 minutes. Components Volume (μL) RNase-free Water To 10 μL 5× gDNA Digester Mix 2 μL Total RNA* 10 pg-5 μg or mRNA* 10 pg-500 ng * It is recommended that the input amount of Total RNA should not exceed 2 μg. If the expression level of the target gene is low, the input amount can be increased to a maximum of 5 μg Total RNA. 2)Reverse Transcription Reaction System Preparation (20 μL System) Components Volume (μL) the reaction solution from the previous step 10 μL 4×Hifair™AdvanceFast SuperMix (No Dye) 5 μL Oligo d(T)18 Primers (50 μmol/L)** 2 μL or Random Primers (* for qPCR) (50 μmol/L)** or 2 μL RNase-free Water To 20 μL * The amount of primers can be adjusted according to the amount of template input. If the reverse transcription product is used for qPCR experiments, Random Primers can be added in the system according to the recommended amount. ** It is recommended to first add 4× Hifair™AdvanceFast SuperMix (No Dye), mix well, and then add the reverse transcription primer to ensure that the primer is not affected by gDNA Digester. 3)Reverse Transcription Procedure Settings Temp. Time 55℃* 5 min** 85℃ 5 sec * For templates with high GC content or complex templates, the reverse transcription temperature can be increased to 60℃. ** This product can synthesize cDNA sequences below 14 kb. If you need longer cDNA products, you can appropriately extend the reverse transcription time. If the experiment does not require the removal of genomic DNA 1)Reverse Transcription Reaction System Preparation (20 μL System) Components Volume (μL) 4×Hifair™AdvanceFast SuperMix (No Dye) 5 μL Oligo d(T)18 Primers (50 μmol/L)** 2 μL or Random Primers (* for qPCR) (50 μmol/L)** or 2 μL Total RNA* 10 pg -5 μg or mRNA 10 pg - 500 ng RNase-free Water To 20 μL * It is recommended that the input amount of Total RNA should not exceed 2 μg. If the expression level of the target gene is low, the input amount can be increased to a maximum of 5 μg Total RNA. ** The amount of primers can be adjusted according to the amount of template input. If the reverse transcription product is used for qPCR experiments, Random Primers can be added in the system according to the recommended amount. 2)Reverse Transcription Procedure Settings Temp. Time 55℃* 5 min** 85℃ 5 sec * For templates with high GC content or complex templates, the reverse transcription temperature can be increased to 60℃. ** This product can synthesize cDNA sequences below 14 kb. If you need longer cDNA products, you can appropriately extend the reverse transcription time. Notes All operations should be performed on ice and should be performed in a manner that avoids RNase contamination. This product is for research use only. Please operate with lab coats and disposable gloves,for your safety. Documents: Safety Data Sheet 11150_MSDS_HB250721.pdf Manuals 11150_Manual_Ver.EN20240201.pdf Related blog: The Reasonable Range of Ct Values in qPCR Experiments